Job Title: Protection and Control EngineerJob DescriptionThe Protection and Control Engineer designs and supports high-voltage utility substation projects, providing technical expertise in protection and control systems, electrical design, and project execution. This role applies industry standards and client guidelines to develop complete engineering design packages, participates in project planning and proposals, and collaborates closely with engineers, designers, and remotely located team members. The position offers a remote work environment with significant exposure to electric utility projects and opportunities for professional growth.Responsibilities<ul><li>Apply knowledge of NEC, NESC, NEMA, ANSI, IEEE, and other industry standards, as well as client standards and applicable guidelines, to develop accurate and compliant engineering designs.</li><li>Provide technical support for client initiatives as a key technical resource under the guidance of an engineering supervisor.</li><li>Work collaboratively in a project team environment with other engineers and designers on detailed electrical design and project management for utility substation projects.</li><li>Participate in project conceptualization, including defining technical approaches, scope, and work plans.</li><li>Contribute to work planning and project execution to ensure deliverables are completed on time and within scope.</li><li>Support pre-bid walkdowns with clients to understand project requirements and site conditions.</li><li>Prepare technical proposals and project estimates for new client projects, helping to define scope, schedule, and resource needs.</li><li>Develop complete design packages for electrical substation systems, including single-line diagrams, AC and DC schematics, wiring diagrams, AC and DC station service diagrams, communication diagrams, SCADA points lists, and other related project deliverables.</li><li>Perform standard substation engineering calculations such as battery sizing calculations, voltage drop analyses, current transformer (CT) saturation checks, and cable sizing calculations.</li><li>Review and ensure the quality of substation design drawings and complete design packages prior to issue.</li><li>Effectively organize and manage multiple, complex assignments and competing priorities to deliver accurate work products on schedule.</li><li>Collaborate effectively with remotely located team members using current collaboration tools and applications.</li><li>Manage project tasks assigned to junior employees, providing guidance and oversight to support their work.</li><li>Travel as needed to support client relationships, pre-bid activities, site visits, and project requirements.</li><li>When appropriate and where in responsible charge, stamp project documents in accordance with professional engineering licensure requirements.</li></ul>Essential Skills<ul><li>Bachelors degree in Electrical Engineering from an accredited college or university.</li><li>At least 5 years of experience in protection and control design.</li><li>Direct, proven expertise in high-voltage projects with voltages up to 500 kV.</li><li>Strong knowledge of protection and control systems for utility substations.</li><li>Experience with substation design, including protection, relays, and control systems.</li><li>Proficiency in electrical design for utility substations and related systems.</li><li>Ability to perform standard substation calculations such as battery, voltage drop, CT saturation, and cable sizing calculations.</li><li>Proficiency in Computer-Aided Design (CAD) software such as AutoCAD, MicroStation, or similar tools.</li><li>Proficiency with CAD systems and current computer applications, including Microsoft applications and design/business enterprise software.</li><li>Ability to work effectively with remotely located team members.</li><li>Demonstrated ability to organize multiple and complex assignments and competing priorities to produce accurate deliverables on time.</li><li>Strong attention to detail and commitment to producing high-quality engineering work.</li><li>Capability to manage project tasks performed by junior employees.</li></ul>Additional Skills &amp; Qualifications<ul><li>Professional Engineer (PE) license is highly preferred, and willingness to stamp projects where in responsible charge.</li><li>Experience with protection and control (P&amp;C) systems and related engineering practices.</li><li>Knowledge and experience with relay systems and relay coordination for substations.</li><li>Experience with PLC programming related to protection and control or substation automation systems.</li><li>Experience preparing proposals and project estimates for electric utility projects.</li><li>Experience participating in pre-bid walkdowns and client-facing technical discussions.</li><li>Comfort with working in a consulting environment supporting a growing team.</li><li>Ability to travel as required to support client relationships and project needs.</li></ul>Work EnvironmentThis role operates in a remote work environment, collaborating primarily through digital platforms such as Microsoft Teams and other standard office and design software. Work is performed using CAD tools, Microsoft applications, and design and business enterprise software to support electric utility substation projects. The position involves coordination with geographically dispersed team members and occasional travel to client sites for walkdowns, meetings, and project-related activities. The environment emphasizes professional collaboration, attention to detail, and the ability to manage multiple complex assignments while supporting a growing consulting team in the electric utility space.Job Type &amp; LocationThis is a Permanent position based out of Pittsburgh, PA.Pay and BenefitsThe pay range for this position is $100000.00 - $180000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.A commitment to excellence and hard work will be rewarded with a competitive salary, career advancement opportunities, and a comprehensive benefits package designed to support your health, financial security, and work-life balance. Our benefits include medical, dental, vision, and prescription drug coverage; a 401(k)-retirement savings plan; and supplemental insurance options. We also provide company-paid life and AD&amp;D insurance, company-paid short-term disability coverage, company-paid maternity and bonding leave, and a generous paid time off program to ensure you have the support and flexibility you need both professionally and personally.Job Type &amp; LocationThis is a Permanent position based out of Pittsburgh, PA.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully remote position.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Protection And Control Engineer

Job Title: Remote Protection and Control EngineerJob DescriptionThe Protection and Control Engineer develops and supports highquality protection and control design packages for transmission and distribution substations. This role prepares detailed engineering drawings and documentation, performs technical studies and calculations, and supports relay settings and coordination activities. The engineer applies industry standards and utility design criteria while collaborating closely with a remote, teamoriented substation and protection and control group.Responsibilities<ul><li>Develop and modify protection and control design packages for transmission and distribution substations.</li><li>Prepare One-Line and Three-Line diagrams, AC/DC elementary schematics, wiring diagrams, protection and control panel layouts, cable schedules, and Bills of Materials.</li><li>Perform engineering calculations and studies related to protection and control systems, including fault analysis and coordination studies as needed.</li><li>Support relay settings development and relay coordination activities for substation protection schemes.</li><li>Apply applicable industry standards, including IEEE, ANSI, NEC, NESC, and utility-specific design criteria, to all protection and control designs.</li><li>Develop and maintain working knowledge of protective relays (such as SEL, GE, ABB, Siemens), transformer protection, line and bus protection, breaker failure schemes, transfer trip schemes, and SCADA and RTU systems.</li><li>Assist with relay setting calculations and the preparation of associated documentation and reports.</li><li>Review and refine protection and control drawings and design packages to ensure accuracy, completeness, and compliance with standards.</li><li>Collaborate closely with the substation and protection and control team to deliver coordinated, constructible designs that meet utility requirements.</li><li>Support quality-focused processes, contributing to consistent, reliable, and safe substation protection and control designs.</li></ul>Essential Skills<ul><li>Associate's or Bachelor's degree in Electrical Engineering or Electrical Engineering Technology.</li><li>3+ years of experience in protection and control engineering, substation design, or relay protection.</li><li>Experience developing and/or reviewing protection and control drawings and design packages.</li><li>Knowledge of utility design standards and engineering practices related to substation and protection and control work.</li><li>Experience with AutoCAD, MicroStation, or similar design platforms for electrical and protection and control design.</li><li>Hands-on experience with protection and control systems, including relays, fault analysis, cable tray layouts, substation design, electrical equipment, and switchgear.</li><li>Ability to interpret and prepare One-Line and Three-Line diagrams, AC/DC schematics, wiring diagrams, and panel layouts.</li><li>Familiarity with applying industry standards such as IEEE, ANSI, NEC, and NESC to protection and control designs.</li><li>Strong attention to detail and ability to produce accurate, consistent engineering documentation.</li><li>Effective communication and collaboration skills for working in a coordinated engineering team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Engineer-in-Training (EIT) certification (nice to have).</li><li>Professional Engineer (PE) license (nice to have).</li><li>Quality assurance and quality control (QA/QC) experience related to engineering design deliverables.</li><li>Experience working with protective relays from manufacturers such as SEL, GE, ABB, and Siemens.</li><li>Exposure to transformer protection, line and bus protection, breaker failure schemes, and transfer trip schemes.</li><li>Familiarity with SCADA and RTU systems in substation applications.</li><li>Interest in learning from Lead Protection and Control Engineers and growing within a substation and protection and control team.</li><li>Motivation to support a large utility system spanning multiple states, with a focus on reliability and safety.</li></ul>Work EnvironmentThis position operates in a remote work environment, with the substation and protection and control team collaborating closely through Microsoft Teams. The team culture emphasizes strong communication, knowledge sharing, and mutual support, providing opportunities to learn from Lead Protection and Control Engineers. The group maintains a healthy backlog of projects, offering steady, engaging work in substation and protection and control design. Work is primarily computer-based, using design platforms such as AutoCAD and MicroStation, along with standard office and collaboration tools in a virtual setting.Job Type &amp; LocationThis is a Contract position based out of Homestead, PA.Pay and BenefitsThe pay range for this position is $45.67 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Homestead, PA.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully remote position.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Position SummaryActalent connects passion with purpose. Our engineering and sciences services and talent solutions capabilities drive results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world.The position falls within Substation Department of the organization. The designer will develop electrical construction drawings for substations. They will mentor lower-level designers.Primary Duties and Responsibilities<ul><li>Work with the latest standards to create drawings for a given project.</li><li>Work with part naming and numbering conventions; and file naming and management protocols.</li><li>Use Vault and ProjectWise for project documentation to track all design modifications and new designs.</li><li>Handle complex projects with minimum supervision.</li><li>Coordinate with people from other departments who are involved in a design project</li><li>Mentor less experienced designers.</li><li>Check and validate drawings for the project and the drawings of peers and subordinates.</li><li>Will work under supervision of Professional Engineers.</li></ul>Protection and Control Focus<ul><li>Create and modify single line diagrams, three-line diagrams, AC &amp; DC schematics, wiring diagrams, cable schedules, or other equipment schematics such as MOABs, circuit breakers, CCVTs, and panel front views using AutoCAD, AutoCAD Electrical, and MicroStation.</li><li>Design protection schemes that deal with breaker controls, line relaying, bus relaying, and communication internal to the station as well as external to the station.</li></ul>Education and Experience Requirements<ul><li>Four plus years of experience designing schematics, wiring diagrams, single line diagrams, and schematics.</li><li>Four plus years of electrical design experience using MicroStation and AutoCAD.</li><li>Demonstrable proficiency using AutoCAD Electrical.</li><li>Associate degree in applied science (AAS) in drafting and computer aided (CAD) design or in civil, electrical or mechanical engineering technology or equivalent experience and/or education.</li></ul>Requisite Abilities and Skills<ul><li>Advanced ability to develop wiring diagrams and cable/conduit tables from schematics</li><li>Advanced knowledge with single line drawings, three-line drawings, fuse and circuit breaker coordination</li><li>Advanced understanding of design practices and engineering systems</li><li>Strong written and verbal communication</li><li>Demonstrate ability to work with others in supplying information and seeking assistance as necessary</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Birmingham, AL.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Birmingham, AL.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully remote position.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Protection And Controls Designer

Job Title: Wire Harness TechnicianJob DescriptionThe Wire Harness Technician will play a pivotal role in launching the company's first in-house wire harness manufacturing initiative. This position is responsible for building wire harnesses for production and pilot programs, developing a quality control and testing process, and supporting Engineering, Quality, and Electrical teams during prototype and validation activities.Responsibilities<ul><li>Build wire harnesses for production needs and prototype harnesses for pilot vehicles.</li><li>Interpret and work from wiring diagrams, schematics, and build instructions.</li><li>Crimp, strip, route, tape, terminate, and test 12V harnesses using industry-standard tools and techniques.</li><li>Validate fit, form, and function of harnesses in vehicle applications.</li><li>Develop and implement an end-to-end quality control process in collaboration with Quality and Engineering teams.</li><li>Establish testing methods, document inspection standards, and maintain accurate build records.</li><li>Assist in developing workflows for the new harness build cell, performing time studies and process evaluations.</li><li>Identify and implement continuous improvement changes, maintaining 5S standards in the harness area.</li><li>Collaborate with the Electrical Team to balance workloads and support Engineering and Quality with various evaluations.</li><li>Participate in pilot builds, engineering reviews, and production readiness activities.</li></ul>Essential Skills<ul><li>Hands-on experience building wire harnesses (12V automotive, upfitting, or similar).</li><li>Ability to read wiring diagrams, schematics, and work instructions.</li><li>Experience with harness testing and quality control, including continuity checks and inspection criteria.</li><li>Understanding of automotive electrical systems, 12V circuits, and related components.</li><li>Strong documentation skills for test procedures and build logs.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience developing a new manufacturing process or launching a new product line.</li><li>Understanding of lean manufacturing and continuous improvement methodologies.</li><li>Experience building prototype harnesses or pilot-phase components.</li><li>Exposure to supplier cost comparisons or make-vs-buy analysis.</li><li>Knowledge of upfitting or vehicle modification operations.</li></ul>Work EnvironmentThis role is based in a newly established harness cell, where you will help set up workflow, quality checks, and layout. The work environment includes hands-on tasks such as crimping, routing, assembly, testing, and documentation. You will collaborate with Engineering, Quality, and Electrical teams in a startup-like manufacturing setting that requires flexibility, problem-solving, and experimentation. The position supports both production needs and prototype/pilot builds for new vehicle programs. You are expected to follow and maintain 5S and safe work practices. The work schedule is 1st shift, 8-5 PM with a flexible start time, allowing you to begin as early as 7 AM.Job Type &amp; LocationThis is a Contract to Hire position based out of Adrian, MI.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Adrian, MI.Application DeadlineThis position is anticipated to close on Oct 30, 2026.Workplace TypeThis is a fully onsite position in Adrian,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Prototype Technician

DescriptionGas vehicle repair technician able to perform all aspects of mechanical repairs to include welding and fabrication work. Capable of electrical diagnoses and wiring repairs. Reading and interpretation of schematics. Extensive written and verbal communication skills, computer skills with ability to utilize Microsoft products. Capable of working within a team environmentBusiness Group emissions work for the government, prep vehicles from an emission standpoint, upfitting of electrical components in the vehicles, communicate well with the team lead and engineers, putting computer stacks, wiring, emission probes metal tube that goes into the vehicle), check temperature, weld fabrication of the exhaust systems, might set the whole vehicle up if something is not working, look into it and fix it Fabrication, electrical component set up and setting up the vehicles Suspension work, break work, dropping the fuel tanks, sometimes tear down engines Job Type &amp; LocationThis is a Contract position based out of Milford, MI.Pay and BenefitsThe pay range for this position is $27.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Milford, MI.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Milford,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Prototype Vehicle Technician Powertrain

<h2>Job Description</h2><ul><li>We are seeking a skilled Vehicle Repair Technician with expertise in gas vehicle repair, mechanical and electrical diagnostics, welding, and fabrication. This role requires reading and interpreting schematics, along with strong communication and computer skills. You will be working closely within a team to ensure the efficiency and safety of government emission vehicles.</li><li></li></ul><h2>Responsibilities</h2><ul><ul><li>Perform mechanical repairs including welding and fabrication.</li><li>Conduct electrical diagnoses and wiring repairs.</li><li>Read and interpret schematics for vehicle systems.</li><li>Prepare vehicles for government emission standards.</li><li>Upfit electrical components and install emission probes.</li><li>Conduct suspension work, brake work, and engine tear-downs.</li><li>Drop fuel tanks and perform exhaustive system fabrications.</li><li>Collaborate effectively with team leads and engineers.</li><li>Participate in weekly business meetings to manage workflows.</li></ul></ul><h2>Essential Skills</h2><ul><ul><li>Mechanical repair and troubleshooting expertise.</li><li>Electrical diagnostic proficiency.</li><li>Mechanical aptitude with the ability to tear apart and repair vehicles.</li><li>Strong wiring repair skills.</li><li>Experience in building wire harnesses and reading schematics.</li></ul></ul><h2>Additional Skills &amp; Qualifications</h2><ul><ul><li>2-year technical degree preferred, but open to candidates with significant experience.</li><li>At least 8-10 years of hands-on experience in vehicle repair.</li><li>Self-motivated, self-starter, and team player.</li><li>Excellent communication skills and problem-solving abilities.</li><li>Optimistic and proactive attitude.</li></ul></ul><h2>Work Environment</h2><ul><li>The work environment is collaborative, involving regular interaction with team leads and engineers. Weekly meetings are conducted to manage business processes effectively. The role may involve working on prolonged repair tickets, with projects lasting 2-3 weeks. The position is driven by high ticket volume and requires flexibility in managing time and tasks.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Milford, MI.Pay and BenefitsThe pay range for this position is $27.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Milford, MI.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Milford,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: Purification Technician III Day ShiftJob DescriptionThe Purification Technician III Day Shift supports downstream biologics manufacturing operations in a cGMP-regulated environment. This role focuses on purification processes, including chromatography and filtration, and requires hands-on operation of manufacturing equipment, execution of batch activities, and meticulous GMP documentation. The technician ensures safe, compliant, and efficient commercial production while collaborating with cross-functional teams and contributing to continuous improvement initiatives.Responsibilities<ul><li>Execute purification manufacturing operations in accordance with current Good Manufacturing Practices (cGMP), standard operating procedures, and batch record requirements.</li><li>Perform downstream processing activities such as chromatography, filtration, buffer preparation, equipment setup, and process monitoring.</li><li>Conduct in-process sampling and testing, including pH and conductivity measurements and visual inspections, to ensure process control and product quality.</li><li>Execute validation protocols following approved procedures and GMP requirements to support qualified and compliant manufacturing processes.</li><li>Utilize manufacturing systems and process control platforms, including Distributed Control Systems (DCS) and Manufacturing Execution Systems (MES), to manage production activities.</li><li>Perform takeouts, identity checks, material transactions, and production-related entries within electronic manufacturing systems.</li><li>Execute cleaning and sanitization activities, including Clean-in-Place (CIP) and Steam-in-Place (SIP) processes, to maintain equipment and facility readiness.</li><li>Maintain accurate, complete, and timely GMP documentation for all manufacturing operations and related activities.</li><li>Support manufacturing investigations and deviation management by identifying issues, documenting observations, and contributing to root cause analysis and corrective actions.</li><li>Participate in continuous improvement initiatives aimed at enhancing safety, quality, and operational efficiency within the manufacturing area.</li><li>Collaborate with cross-functional teams to ensure safe, compliant, and efficient production operations and effective communication across functions.</li><li>Participate in shift turnover activities, clearly communicating process status, issues, and priorities to incoming teams.</li><li>Identify and document deviations and initiate maintenance work orders when necessary to address equipment or process concerns.</li><li>Support production schedules and meet operational timelines in a fast-paced biologics manufacturing environment.</li><li>Perform other duties as assigned to support overall manufacturing objectives.</li></ul>Essential Skills<ul><li>Strong written and verbal communication skills to document activities and interact effectively with team members.</li><li>Knowledge of cGMP regulations and safety requirements applicable to biopharmaceutical manufacturing operations.</li><li>Ability to work effectively in a team environment and collaborate with cross-functional groups.</li><li>Strong time management skills and attention to detail to execute complex manufacturing processes accurately.</li><li>Ability to identify and document deviations and initiate maintenance work orders when necessary.</li><li>Ability to exercise sound judgment, work independently, and solve problems in a manufacturing environment.</li><li>Ability to support production schedules in a fast-paced biologics manufacturing facility.</li><li>Hands-on experience with purification, chromatography, and filtration processes in a manufacturing setting.</li><li>Comfort using manufacturing systems and process control platforms such as DCS and MES.</li><li>Capability to perform cleaning and sanitization activities, including CIP and SIP processes.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or GED with 4+ years of experience in a cGMP manufacturing environment; OR Associate degree in Life Sciences, Engineering, or a related technical discipline with 2+ years of cGMP manufacturing experience; OR Bachelors degree in Life Sciences, Engineering, or a related technical discipline; OR equivalent military training or experience.</li><li>Experience supporting purification, chromatography, filtration, recovery, or other downstream manufacturing operations.</li><li>Experience working within a GMP-regulated biologics, biotechnology, or pharmaceutical manufacturing environment.</li><li>Familiarity with automated manufacturing control systems and electronic batch records.</li><li>Experience operating AKTA systems, chromatography skids, tangential flow filtration (TFF) systems, depth filtration equipment, or other downstream processing equipment.</li><li>BioWork certification.</li><li>Ability to stand for extended periods while performing manufacturing tasks.</li><li>Ability to perform repetitive tasks using hands, wrists, and fingers for equipment operation and documentation.</li><li>Ability to bend, push, pull, reach, and lift materials up to 33 pounds as part of routine manufacturing activities.</li><li>Ability to ascend and descend ladders and access manufacturing equipment safely.</li><li>Ability to work in manufacturing environments requiring personal protective equipment, including respiratory protection when necessary.</li><li>Ability to work in temperature-variable manufacturing environments.</li></ul>Work EnvironmentThis position is based in an onsite biologics manufacturing facility operating under cGMP regulations. The role is assigned to the day shift on a 2-2-3 rotation schedule, supporting commercial downstream purification operations. The environment includes regular use of purification equipment such as chromatography systems, filtration units, and automated manufacturing control platforms including DCS and MES. Work is performed in production areas that may have variable temperatures and require the use of personal protective equipment, including respiratory protection when needed. The role involves standing for extended periods, performing repetitive manual tasks, lifting materials up to 33 pounds, and accessing equipment via ladders. The facility emphasizes safety, quality, and teamwork, with structured shift turnover practices and a focus on continuous improvement to maintain efficient and compliant operations.Job Type &amp; LocationThis is a Contract position based out of Morrisville, NC.Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Morrisville, NC.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Morrisville,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Purification Technician III  Day Shift

Job Title: Purification Technician III Night ShiftJob DescriptionThe Purification Technician III Night Shift supports downstream biologics manufacturing operations in a cGMP-regulated environment. This role focuses on purification processes such as chromatography and filtration and involves hands-on operation of manufacturing equipment, execution of batch activities, and meticulous GMP documentation. The technician ensures safe, compliant, and efficient commercial production while collaborating with cross-functional teams and contributing to continuous improvement initiatives.Responsibilities<ul><li>Execute purification manufacturing operations in accordance with current Good Manufacturing Practices (cGMP), standard operating procedures, and batch record requirements.</li><li>Perform downstream processing activities including chromatography, filtration, buffer preparation, equipment setup, and process monitoring.</li><li>Conduct in-process sampling and testing, including pH and conductivity measurements and visual inspections, to maintain process control and product quality.</li><li>Execute validation protocols following approved procedures and GMP requirements to support qualified and compliant manufacturing processes.</li><li>Use manufacturing systems and process control platforms, including Distributed Control Systems (DCS) and Manufacturing Execution Systems (MES), to manage production activities.</li><li>Perform takeouts, identity checks, material transactions, and production-related entries within electronic manufacturing systems.</li><li>Carry out cleaning and sanitization activities, including Clean-in-Place (CIP) and Steam-in-Place (SIP) processes, to maintain equipment and facility readiness.</li><li>Maintain accurate, complete, and timely GMP documentation for all manufacturing operations and related activities.</li><li>Support manufacturing investigations and deviation management by identifying issues, documenting observations, and contributing to root cause analysis and corrective and preventive actions.</li><li>Participate in continuous improvement initiatives to enhance safety, quality, and operational efficiency within the manufacturing area.</li><li>Collaborate with cross-functional teams to ensure safe, compliant, and efficient production operations and effective communication across functions.</li><li>Participate in shift turnover activities, clearly communicating process status, issues, and priorities to incoming teams.</li><li>Identify and document deviations and initiate maintenance work orders when necessary to address equipment or process concerns.</li><li>Support production schedules and meet operational timelines in a fast-paced biologics manufacturing environment.</li><li>Perform other duties as assigned to support overall manufacturing objectives.</li></ul>Essential Skills<ul><li>Strong written and verbal communication skills to document activities clearly and interact effectively with team members.</li><li>Knowledge of cGMP regulations and safety requirements applicable to biopharmaceutical manufacturing operations.</li><li>Ability to work effectively in a team environment and collaborate with cross-functional groups.</li><li>Strong time management skills and attention to detail to execute complex manufacturing processes accurately.</li><li>Ability to identify and document deviations and initiate maintenance work orders when necessary.</li><li>Ability to exercise sound judgment, work independently, and solve problems in a manufacturing environment.</li><li>Ability to support production schedules in a fast-paced biologics manufacturing facility.</li><li>Hands-on experience with purification, chromatography, and filtration processes in a manufacturing setting.</li><li>Comfort using manufacturing systems and process control platforms such as DCS and MES.</li><li>Capability to perform cleaning and sanitization activities, including CIP and SIP processes.</li><li>Strong understanding of GMP documentation, batch records, deviations, in-process sampling and testing, and equipment cleaning and sanitization.</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or GED with 4+ years of experience in a cGMP manufacturing environment; OR an Associate degree in Life Sciences, Engineering, or a related technical discipline with 2+ years of cGMP manufacturing experience; OR a Bachelors degree in Life Sciences, Engineering, or a related technical discipline; OR equivalent military training or experience.</li><li>Experience supporting purification, chromatography, filtration, recovery, or other downstream manufacturing operations.</li><li>Experience working within a GMP-regulated biologics, biotechnology, or pharmaceutical manufacturing environment.</li><li>Familiarity with automated manufacturing control systems and electronic batch records.</li><li>Experience operating AKTA systems, chromatography skids, tangential flow filtration (TFF) systems, depth filtration equipment, or comparable downstream processing equipment.</li><li>BioWork certification.</li><li>Experience with biologics purification, including chromatography, filtration/TFF, and buffer preparation in a cGMP manufacturing environment.</li><li>Ability to work an overnight night-shift schedule on a 2-2-3 rotation.</li><li>Ability to stand for extended periods while performing manufacturing tasks.</li><li>Ability to perform repetitive tasks using hands, wrists, and fingers for equipment operation and documentation.</li><li>Ability to bend, push, pull, reach, and lift materials up to 33 pounds as part of routine manufacturing activities.</li><li>Ability to ascend and descend ladders and access manufacturing equipment safely.</li><li>Ability to work in manufacturing environments requiring personal protective equipment, including respiratory protection when necessary.</li><li>Ability to work in temperature-variable manufacturing environments.</li></ul>Work EnvironmentThis role is based in an onsite biologics manufacturing facility operating under cGMP regulations and is assigned to the night shift on a 2-2-3 rotation schedule, supporting commercial downstream purification operations. Work takes place in production areas that use purification equipment such as chromatography systems, filtration units, and automated manufacturing control platforms including DCS and MES. The environment may have variable temperatures and requires the use of personal protective equipment, including respiratory protection when needed. The position involves standing for extended periods, performing repetitive manual tasks, lifting materials up to 33 pounds, and accessing equipment via ladders. The facility emphasizes safety, quality, and teamwork, with structured shift turnover practices and a strong focus on continuous improvement to maintain efficient and compliant operations.Job Type &amp; LocationThis is a Contract position based out of Morrisville, NC.Pay and BenefitsThe pay range for this position is $38.00 - $43.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Morrisville, NC.Application DeadlineThis position is anticipated to close on Nov 3, 2026.Workplace TypeThis is a fully onsite position in Morrisville,NC.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Purification Technician III  Night Shift

QA Document Review AssociateINTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO JABRUNNER @ACTALENTSERVICES .COM OR TEXT JAKE AT 614. 726. 7399 TO SET UP AN IMMEDIATE PHONE INTERVIEW!Job DescriptionThe QA Document Review Associate is a vital part of the Environmental Condition Team, responsible for ensuring the manufacture of safe and effective pharmaceuticals. This role involves performing quality compliance reviews of cGMP analytical data and results from the QC Microbiology and Environmental Monitoring team, facilitating corrections and clarifications, and providing final approval of records.Responsibilities<ul><li>Provide quality assurance reviews of laboratory raw data and reports, including environmental monitoring and microbiological worksheets, test summaries, and trending data.</li><li>Participate in identifying quality process improvements to enhance system, operation, and personnel efficiencies related to the QA Data Review process.</li><li>Write and revise SOPs and other GMP documentation as needed and initiate and complete the Change Request process.</li><li>Maintain accurate records of work performed in LIMS and Laboratory systems according to Good Documentation Practices, SOPs, and policies.</li><li>Assist with data for trending and report deviations from Out-of-Specification results.</li><li>Communicate any discrepancies or deviations to supervision or management upon discovery.</li><li>Ensure all work is performed and documented in accordance with existing company policies, procedures, Current Good Manufacturing Practices, and health and safety requirements.</li><li>Plan daily workload to meet requirements and maintain compliance with all required SOPs.</li></ul>Essential Skills<ul><li>Bachelors degree in Biological, Physical Sciences, Mathematics, or a related field, or an Associate Degree with experience in data review.</li><li>Extreme attention to detail to achieve quality results.</li><li>Experience in documentation and highly regulated fields.</li><li>Excellent communication, organization, and project management skills.</li><li>Proficiency in Microsoft Office (PowerPoint, Excel, Word).</li><li>Ability to work independently and collaboratively in a diverse and inclusive environment.</li><li>Handling confidential information with the ability to maintain confidentiality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in documentation is preferred.</li><li>Experience in highly regulated fields is preferred.</li></ul>Work EnvironmentThis position is primarily desk-based but requires walking around the facility to collect data and information. The dress code is business casual. The work hours are from 8:30 AM to 5:00 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Application DeadlineThis position is anticipated to close on Nov 8, 2026.Workplace TypeThis is a fully onsite position in Columbus,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Document Review Associate

QA InspectorSchedule a time here for more information! https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxlThe QA/QC Inspector performs in-process and finished goods inspections within a clinical label manufacturing environment. This role focuses on inspecting labels and production materials, identifying and documenting quality issues, and ensuring that all products meet established quality and regulatory requirements.Responsibilities<ul><li>Perform visual and automated quality inspections at multiple stages throughout the manufacturing process.</li><li>Inspect pharmaceutical labels for accuracy, legibility, alignment, print quality, and overall compliance with specifications and regulatory requirements.</li><li>Set up, monitor, and perform routine checks on automatic inspection equipment to ensure proper operation.</li><li>Identify defects, non-conformities, and deviations from specifications in labels and production materials.</li><li>Document inspection results clearly and accurately, and maintain complete and organized quality records.</li><li>Report quality issues, inspection findings, and trends promptly to supervision or management.</li><li>Troubleshoot inspection issues and assist in identifying root causes and implementing corrective actions.</li><li>Maintain production pace while consistently ensuring that quality standards and regulatory requirements are met.</li></ul>Essential Skills<ul><li>Minimum 1 year of experience in quality assurance (QA), quality control (QC), or a closely related field.</li><li>Experience working in a cGMP (current Good Manufacturing Practice) environment.</li><li>Experience with automated inspection equipment in a manufacturing or packaging setting.</li><li>Strong attention to detail and accuracy in visual and automated inspections.</li><li>Proficiency in documenting inspection results and maintaining quality records.</li><li>Troubleshooting and problem-solving skills related to inspection processes and equipment.</li><li>Ability to work effectively in a fast-paced, team-oriented manufacturing environment.</li><li>High school diploma or equivalent.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with pharmaceutical or clinical label review.</li><li>Quality assurance, quality control, or quality inspection within a manufacturing environment.</li><li>Familiarity with batch record review and documentation practices.</li><li>Comfort performing overnight work on a consistent schedule.</li></ul>Work EnvironmentThis role is based in a clinical label manufacturing facility that operates on a 3rd shift schedule from 11:00 PM to 7:30 AM. The environment is fast-paced and team-oriented, with a strong focus on compliance with cGMP standards and quality control procedures. The QA/QC Inspector works closely with production teams and uses both visual methods and automated inspection equipment to evaluate labels and materials. The position requires sustained attention to detail, consistent documentation, and the ability to maintain productivity while upholding strict quality and regulatory standards.Job Type &amp; LocationThis is a Permanent position based out of Bohemia, NY.Pay and BenefitsThe pay range for this position is $24.00 - $29.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Bohemia, NY.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Bohemia,NY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Inspector

QA InspectorThe QA/QC Inspector performs in-process and finished goods inspections within a clinical label manufacturing environment. This role focuses on inspecting labels and production materials, identifying and documenting quality issues, and ensuring that all products meet established quality and regulatory requirements.Responsibilities<ul><li>Perform visual and automated quality inspections at multiple stages throughout the manufacturing process.</li><li>Inspect pharmaceutical labels for accuracy, legibility, alignment, print quality, and overall compliance with specifications and regulatory requirements.</li><li>Set up, monitor, and perform routine checks on automatic inspection equipment to ensure proper operation.</li><li>Identify defects, non-conformities, and deviations from specifications in labels and production materials.</li><li>Document inspection results clearly and accurately, and maintain complete and organized quality records.</li><li>Report quality issues, inspection findings, and trends promptly to supervision or management.</li><li>Troubleshoot inspection issues and assist in identifying root causes and implementing corrective actions.</li><li>Maintain production pace while consistently ensuring that quality standards and regulatory requirements are met.</li></ul>Essential Skills<ul><li>Minimum 1 year of experience in quality assurance (QA), quality control (QC), or a closely related field.</li><li>Experience working in a cGMP (current Good Manufacturing Practice) environment.</li><li>Experience with automated inspection equipment in a manufacturing or packaging setting.</li><li>Strong attention to detail and accuracy in visual and automated inspections.</li><li>Proficiency in documenting inspection results and maintaining quality records.</li><li>Troubleshooting and problem-solving skills related to inspection processes and equipment.</li><li>Ability to work effectively in a fast-paced, team-oriented manufacturing environment.</li><li>High school diploma or equivalent.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with pharmaceutical or clinical label review.</li><li>Quality assurance, quality control, or quality inspection within a manufacturing environment.</li><li>Familiarity with batch record review and documentation practices.</li><li>Comfort performing overnight work on a consistent schedule.</li></ul>Work EnvironmentThis role is based in a clinical label manufacturing facility that operates on a 3rd shift schedule from 11:00 PM to 7:30 AM. The environment is fast-paced and team-oriented, with a strong focus on compliance with cGMP standards and quality control procedures. The QA/QC Inspector works closely with production teams and uses both visual methods and automated inspection equipment to evaluate labels and materials. The position requires sustained attention to detail, consistent documentation, and the ability to maintain productivity while upholding strict quality and regulatory standardsJob Type &amp; LocationThis is a Permanent position based out of Bohemia, NY.Pay and BenefitsThe pay range for this position is $24.00 - $29.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Bohemia, NY.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Bohemia,NY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QA Receiving TechnicianJob DescriptionThe QA Receiving Technician is responsible for monitoring, inspecting, documenting, and validating incoming materials and production quality activities within a food manufacturing environment. This role serves as a key quality resource by ensuring raw materials, packaging, and finished products meet company specifications and food safety requirements. The ideal candidate is detail-oriented, organized, and comfortable working both independently and cross-functionally with production, inventory, receiving, and quality teams.Responsibilities<ul><li>Inspect incoming raw materials, spices, ingredients, and packaging materials.</li><li>Compare incoming materials to approved specifications and requirements.</li><li>Review and maintain Certificates of Analysis (COAs).</li><li>Request missing specifications and documentation as needed.</li><li>Receive and document damaged goods and non-conforming materials.</li><li>Complete quality reports including condemnation, foreign material, and mislabeling documentation.</li><li>Collect and maintain supporting documentation and photographs when required.</li><li>Maintain accurate records and quality documentation.</li><li>Initiate quality holds and quarantine activities when necessary.</li><li>Perform post-production quality checks including package seal integrity, Modified Atmosphere Packaging (MAP) verification, and drain weight evaluations.</li><li>Conduct routine chemical testing and analysis in the laboratory.</li><li>Verify product quality throughout production processes.</li><li>Conduct internal quality audits including warehouse inspections, pest control audits, and facility and grounds inspections.</li><li>Support food safety and quality initiatives.</li><li>Assist with HACCP-related documentation and compliance activities.</li></ul>Essential Skills<ul><li>Quality assurance</li><li>Data entry</li><li>Raw material testing</li><li>Experience accurately documenting quality and production information</li><li>Ability to inspect incoming raw materials and compare findings against specifications</li><li>Experience reviewing COAs and quality documentation</li><li>Strong attention to detail and data entry accuracy</li><li>Comfortable working independently in a production environment</li><li>HACCP</li><li>Laboratory</li><li>Quality audits</li><li>Chemical analysis</li><li>Inventory management</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma or GED</li><li>Minimum 1 year of quality, manufacturing, production, laboratory, or related experience</li><li>Strong documentation and recordkeeping skills</li><li>Basic computer skills including Microsoft Excel and Word</li><li>Ability to work independently with minimal supervision</li><li>Strong mathematical and analytical skills</li><li>Ability to accurately record and communicate quality information</li><li>Food manufacturing experience</li><li>Pharmaceutical, biotech, or regulated manufacturing experience</li><li>HACCP exposure</li><li>Laboratory testing experience</li><li>Auditing experience</li><li>Bilingual English/Spanish</li></ul>Work EnvironmentThis position operates within a food manufacturing facility and laboratory environment. Employees frequently move between production, receiving, warehouse, and quality areas while monitoring product quality and food safety. Working conditions include exposure to wet and manufacturing environments, moving equipment and machinery, occasional exposure to hot, cold, and outdoor conditions, and frequent standing, walking, lifting, and bending. The schedule is Monday - Friday on a swing shift from 4:00 PM to 1:30 AM, with overtime potentially required based on operational needs. The team structure includes approximately 20 employees supported per shift.Job Type &amp; LocationThis is a Permanent position based out of Woodburn, OR.Pay and BenefitsThe pay range for this position is $42640.00 - $42640.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Medical
dental
vision
HSA
EAP
RX programJob Type &amp; LocationThis is a Permanent position based out of Woodburn, OR.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Woodburn,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Receiving Technician

Job Title: QA Receiving TechnicianJob DescriptionThe QA Receiving Technician is responsible for monitoring, inspecting, documenting, and validating incoming materials and production quality activities within a food manufacturing environment. This role serves as a key quality resource by ensuring raw materials, packaging, and finished products consistently meet established specifications and food safety requirements. The position suits a detail-oriented, organized individual who is comfortable working both independently and collaboratively with production, inventory, receiving, and quality teams.Responsibilities<ul><li>Inspect incoming raw materials, spices, ingredients, and packaging materials to ensure they meet approved specifications and requirements.</li><li>Compare incoming materials against documented specifications and quality standards and identify any non-conforming materials.</li><li>Review, maintain, and organize Certificates of Analysis (COAs) and other quality documentation for incoming materials.</li><li>Request missing specifications, COAs, and supporting documentation from appropriate internal or external contacts as needed.</li><li>Receive, document, and report damaged goods and non-conforming materials in accordance with quality procedures.</li><li>Complete detailed quality reports, including condemnation reports, foreign material reports, and mislabeling documentation.</li><li>Collect and maintain supporting documentation, photographs, and evidence for quality incidents when required.</li><li>Maintain accurate records and quality documentation to support traceability and compliance requirements.</li><li>Initiate quality holds and quarantine activities for suspect or non-conforming materials and products when necessary.</li><li>Perform post-production quality checks, including package seal integrity verification, Modified Atmosphere Packaging (MAP) checks, and drain weight evaluations.</li><li>Conduct routine chemical testing and analysis in the laboratory to verify product quality and compliance.</li><li>Verify product quality throughout production processes by performing in-process checks and documenting results.</li><li>Conduct internal quality audits, including warehouse inspections, pest control audits, and facility and grounds inspections.</li><li>Support food safety and quality initiatives by following established procedures and participating in improvement activities.</li><li>Assist with HACCP-related documentation and compliance activities, ensuring records are complete and accurate.</li><li>Accurately enter and manage quality and production data in electronic and paper-based systems.</li><li>Communicate quality findings clearly and promptly to production, inventory, receiving, and quality teams.</li><li>Work independently in a production and laboratory environment while following all safety and quality protocols.</li></ul>Essential Skills<ul><li>High School Diploma or GED.</li><li>Minimum 1 year of experience in quality, manufacturing, production, laboratory, or a related environment.</li><li>Experience accurately documenting quality and production information in a structured format.</li><li>Ability to inspect incoming raw materials and compare findings against established specifications.</li><li>Experience reviewing Certificates of Analysis (COAs) and related quality documentation.</li><li>Strong attention to detail with a high level of data entry accuracy.</li><li>Strong documentation and recordkeeping skills to maintain organized and complete quality records.</li><li>Basic computer skills, including the ability to use Microsoft Excel and Word for data entry and reporting.</li><li>Ability to work independently with minimal supervision while meeting deadlines and quality expectations.</li><li>Strong mathematical and analytical skills for measurements, calculations, and data evaluation.</li><li>Ability to accurately record and communicate quality information to cross-functional teams.</li><li>Comfort working in a production and food manufacturing environment with established safety and quality procedures.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in food manufacturing environments.</li><li>Experience in pharmaceutical, biotech, or other regulated manufacturing settings.</li><li>Exposure to HACCP principles and food safety programs.</li><li>Laboratory testing experience, including routine chemical analysis.</li><li>Experience conducting quality audits such as warehouse, pest control, or facility inspections.</li><li>Bilingual English/Spanish communication skills.</li><li>Interest in gaining experience in quality assurance and food safety.</li><li>Motivation to learn HACCP and quality systems and participate in continuous improvement.</li><li>Desire to work in a fast-paced manufacturing environment with opportunities for growth.</li><li>Comfort interacting with production, laboratory, inventory, receiving, and food safety operations in a cross-functional setting.</li></ul>Work EnvironmentThis position operates within a food manufacturing facility and laboratory environment on a Monday through Friday day shift schedule, typically from 6:00 AM to 2:30 PM, with overtime that may be required based on operational needs. The role supports approximately 20 employees per shift and involves frequent movement between production, receiving, warehouse, and quality areas while monitoring product quality and food safety. Working conditions include exposure to a wet manufacturing environment, moving equipment and machinery, and occasional exposure to hot, cold, and outdoor conditions. The position requires frequent standing, walking, lifting, and bending, and adherence to all facility safety, quality, and hygiene practices appropriate for a food production and laboratory setting.Job Type &amp; LocationThis is a Permanent position based out of Woodburn, OR.Pay and BenefitsThe pay range for this position is $40560.00 - $40560.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Medical
dental
vision
HSA
EAP
RX programJob Type &amp; LocationThis is a Permanent position based out of Woodburn, OR.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Woodburn,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QA SpecialistJob DescriptionThe QA Specialist supports all elements of the quality system to ensure compliance with FDA cGMP and other applicable quality standards, with a primary focus on Supplier Quality. This role manages supplier qualification activities, oversees supplier-related quality documentation, and collaborates closely with internal and external stakeholders to maintain robust, audit-ready quality systems within a pharmaceutical environment.Responsibilities<ul><li>Support all quality system elements to ensure compliance with FDA cGMP and other relevant quality standards, with an emphasis on Supplier Quality.</li><li>Manage supplier qualification activities for new and existing suppliers, ensuring they meet internal and regulatory requirements.</li><li>Coordinate supplier onboarding through the development and review of supplier qualification questionnaires, quality agreements, paper audits, and supporting documentation.</li><li>Review, process, and support supplier-related change controls, ensuring appropriate assessment, documentation, and implementation.</li><li>Assess supplier quality documentation to verify compliance with internal quality requirements and regulatory expectations.</li><li>Support the qualification of suppliers providing APIs, raw materials, components, packaging materials, bottles, pails, bags, contract manufacturing services (CMOs), and external laboratory services.</li><li>Track and manage supplier qualification projects from initiation through approval, maintaining clear timelines and status updates.</li><li>Communicate directly with suppliers regarding qualification requirements, documentation requests, and quality-related inquiries.</li><li>Support supplier risk assessments and supplier quality evaluations to identify and mitigate potential quality risks.</li><li>Participate in supplier audit preparation and follow-up activities, including documentation review and paper-based audits.</li><li>Maintain supplier qualification records and ensure all documentation is complete, accurate, and audit-ready.</li><li>Collaborate with internal stakeholders to resolve supplier quality issues and support continuous improvement initiatives within the quality system.</li><li>Assist with Annual Product Reviews (APRs) and related quality documentation, as applicable.</li><li>Contribute to the overall effectiveness of Quality Assurance and Quality Systems by supporting activities such as change control, label control, APRs, and other quality system processes.</li></ul>Essential Skills<ul><li>3+ years of experience in a FDA-regulated pharmaceutical facility preferred.</li><li>3+ years of experience in Quality Assurance and/or Quality Systems.</li><li>Demonstrated exposure to and experience with Quality Systems, preferably including Supplier Quality, Change Control, Label Control, and Annual Product Reviews.</li><li>Strong experience in supplier qualification, including hands-on work with supplier qualification questionnaires, quality agreements, change controls, paper-based audits, supplier documentation, and qualification requirements.</li><li>Knowledge of Annual Product Reviews (APRs) and related processes.</li><li>Experience working in a pharmaceutical environment with an understanding of regulatory expectations and quality standards.</li><li>Familiarity with quality systems management, supplier quality, auditing practices, and quality management principles.</li><li>Proficiency in MS Office tools, including Word, Excel, and Outlook.</li><li>Strong verbal, written, and electronic communication skills to effectively interact with suppliers and internal stakeholders.</li><li>Ability to manage multiple supplier qualification projects and documentation in an organized, detail-oriented, and audit-ready manner.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree strongly preferred.</li><li>Degree in Biology, Chemistry, or a related scientific field preferred.</li><li>Experience with regulatory submissions and regulatory affairs is beneficial.</li><li>Experience working with CMOs and external laboratories is an advantage.</li><li>Strong customer focus, integrity, and commitment to safety and compliance.</li><li>Demonstrated ability to collaborate effectively within cross-functional teams.</li><li>Proven track record of achieving results in a quality-focused environment.</li><li>Interest in learning multiple areas of quality systems and expanding expertise within Quality Assurance.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of St. Louis, MO.Pay and BenefitsThe pay range for this position is $26.44 - $34.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of St. Louis, MO.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in St. Louis,MO.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Specialist

Job Title: QA SpecialistJob DescriptionThe QA Specialist ensures that all manufacturing documentation and quality system activities comply with cGMP, Good Documentation Practices (GDP), and internal quality standards before product release. In this role, you review batch records and supporting documentation, prepare and verify Certificates of Analysis, manage key quality system processes, and support investigations and continuous improvement initiatives. You play a critical role in making sure products are safe, compliant, and ready for the consumer market.Responsibilities<ul><li>Review batch records and all supporting documentation for accuracy, completeness, and compliance with cGMP and Good Documentation Practices prior to final approval and product release.</li><li>Verify calculations, specifications, and manufacturing data to ensure documentation meets internal quality standards and customer requirements.</li><li>Prepare and review Certificates of Analysis (COAs) and other required quality and manufacturing documentation.</li><li>Manage quality system activities including deviations, corrective and preventive actions (CAPAs), change controls and change orders, quality alerts, customer complaints, and Annual Product Reviews in accordance with standard operating procedures and customer or partner agreements.</li><li>Support and prepare investigations related to deviations and other quality events, ensuring issues are properly documented, thoroughly investigated, and justified.</li><li>Monitor open quality events and follow up with appropriate teams to ensure assigned actions are completed accurately and on time.</li><li>Review responses to customer quality needs to ensure they are complete, accurate, and delivered in a timely manner.</li><li>Perform monthly quality data analysis and reporting to identify trends, recurring issues, and opportunities for improvement.</li><li>Collaborate cross-functionally with manufacturing and other departments to maintain strong quality and compliance standards.</li><li>Support continuous improvement initiatives by applying Lean Manufacturing principles, 5S, and other Lean tools to improve processes and eliminate waste.</li><li>Assist with writing deviations, investigations, and other quality documentation to support overall compliance with the companys quality systems.</li><li>Perform additional duties as assigned to support the quality assurance function and business needs.</li></ul>Essential Skills<ul><li>Bachelors degree in a scientific discipline or related field, or equivalent education and experience.</li><li>3+ years of quality experience in a cGMP manufacturing environment.</li><li>Strong knowledge of cGMP, GDP, and quality documentation requirements.</li><li>Hands-on experience with quality systems, including deviations, CAPAs, investigations, change controls, and batch record review.</li><li>Proficiency in reviewing and verifying manufacturing data, calculations, and specifications.</li><li>Strong analytical skills with the ability to interpret quality data, identify trends, and propose improvements.</li><li>Excellent written and verbal communication skills to document findings clearly and interact effectively with cross-functional teams.</li><li>Exceptional attention to detail and accuracy in documentation and data review.</li><li>Ability to manage multiple quality events and tasks simultaneously while meeting deadlines.</li><li>Comfort working with paper-based quality systems and performing repetitive documentation review and data entry.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with Lean Manufacturing or continuous improvement initiatives, including application of 5S and other Lean tools.</li><li>Quality-related certification such as ASQ, Certified Quality Auditor (CQA), or Certified Quality Manager (CQM).</li><li>Ability to work collaboratively with manufacturing, operations, and other departments in a fast-paced environment.</li><li>Demonstrated ability to respond and adapt to changes in processes, priorities, and workload.</li><li>Interest in career growth, with potential to progress into QA Analyst or advanced QA Specialist roles after 23 years.</li><li>Strong organizational skills and the ability to manage workload with a high degree of autonomy.</li></ul>Work EnvironmentThis is a full-time QA Specialist position working a consistent daytime schedule with a typical start time between 7:00 AM and 9:00 AM. The role is fully onsite at a manufacturing facility and is primarily office-based, with your own cubicle and autonomy to manage your day and workload. The environment offers exposure to a diverse range of products, including beauty, bath and body items, lip balms, skincare, sunscreens, cleaning detergents, and other personal care and OTC products, providing broad manufacturing and quality experience. The facility operates with paper-based quality systems, requiring continuous sitting, talking, and hand/wrist movement for keyboarding for six or more hours per day. Physical requirements include occasional bending, pushing, pulling, climbing stairs, reaching, lifting, grasping, standing, and walking. Sensory requirements include good eyesight, normal hearing, and the ability to speak clearly and be understood in English. You will experience continuous exposure to chemicals and fragrances used in personal care and OTC products and may encounter elevated levels of various fragrances at times. You must be able to use stairways, adapt to changes in the work environment, and work effectively in a high-paced setting. The position may require some work hours beyond the normal workday based on business demands, customer volume, and specific sales efforts. The company offers accruable paid time off, several paid days off, and holiday benefits, along with opportunities for growth as the organization continues to expand at a strong rate year over year.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $26.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Eden Prairie,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h3>QA Batch Record Reviewer / Quality Assurance Specialist</h3><h3>Job Overview:</h3>The QA Batch Record Reviewer will support Quality Assurance operations within a regulated manufacturing environment by ensuring batch documentation, investigations, and quality systems activities comply with GMP, GDP, FDA, and ISO 13485 requirements. This individual will play a key role in batch record review, material release activities, deviation investigations, CAPAs, change controls, and SOP development to support product quality and regulatory compliance.<h3></h3><h3>Key Responsibilities</h3><ul><li>Perform detailed review of batch production records and manufacturing documentation to ensure completeness, accuracy, and compliance prior to product release.</li><li>Review incoming raw material and component documentation for approval and release into inventory.</li><li>Support investigations for major, minor, and critical deviations, identifying root causes and assisting with implementation of corrective and preventive actions (CAPAs).</li><li>Participate in nonconformance investigations and quality event management activities.</li><li>Author, revise, and maintain Standard Operating Procedures (SOPs), work instructions, and quality documentation.</li><li>Create, review, and process change controls to support continuous improvement initiatives and operational changes.</li><li>Ensure all QA documentation practices adhere to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), FDA regulations, and ISO 13485 standards.</li><li>Collaborate cross-functionally with Manufacturing, Quality Control, Regulatory Affairs, and Supply Chain teams to resolve quality-related issues.</li><li>Assist with internal audits, inspections, and readiness activities for regulatory and customer audits.</li><li>Maintain accurate records within quality management systems and support data trending and quality metrics reporting.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Life Sciences, Biology, Chemistry, Biomedical Engineering, or a related scientific discipline preferred.</li><li>1-2 years of Quality Assurance experience within a GMP-regulated environment.</li><li>Experience reviewing batch records, manufacturing documentation, or quality records.</li><li>Working knowledge of GMP, GDP, FDA regulations, and quality systems.</li><li>Familiarity with deviation investigations, CAPAs, change controls, and document control processes.</li><li>Experience operating within an ISO 13485 regulated environment strongly preferred.</li><li>Strong attention to detail, organizational skills, and ability to manage multiple priorities.</li></ul><h3>Preferred Experience</h3><ul><li>Medical device, pharmaceutical, biotechnology, or combination product industry experience.</li><li>Exposure to electronic quality management systems (eQMS).</li><li>Experience supporting audits and regulatory inspections.</li><li>Knowledge of root cause analysis methodologies and risk assessment tools.</li></ul><h3>Key Skills</h3><ul><li>Quality Assurance</li><li>Batch Record Review</li><li>GMP Compliance</li><li>GDP Documentation</li><li>Deviation Investigations</li><li>CAPA Management</li><li>Change Control</li><li>SOP Authoring</li><li>Material Release</li><li>FDA Regulations</li><li>ISO 13485</li><li>Root Cause Analysis</li><li>Document Control</li></ul>Job Type &amp; LocationThis is a Contract position based out of Allendale, NJ.Pay and BenefitsThe pay range for this position is $26.00 - $28.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Allendale, NJ.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Allendale,NJ.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Assurance SpecialistFully Onsite | Long-Term Opportunity | Day Shift Hours Job DescriptionThe QA Specialist ensures that all manufacturing documentation and quality system activities comply with cGMP and internal quality standards before product release. In this role, you review batch records and supporting documentation, prepare and verify Certificates of Analysis, manage key quality system processes, and support investigations and continuous improvement initiatives. You play a critical role in making sure products are safe, compliant, and ready for the consumer market.Responsibilities<ul><li>Review batch records and all supporting documentation for accuracy, completeness, and compliance with cGMP and Good Documentation Practices prior to final approval and product release.</li><li>Verify calculations, specifications, and manufacturing data to ensure documentation meets internal quality standards and customer requirements.</li><li>Prepare and review Certificates of Analysis (COAs) and other required quality and manufacturing documentation.</li><li>Manage quality system activities including deviations, corrective and preventive actions (CAPAs), change controls and change orders, quality alerts, customer complaints, and Annual Product Reviews in accordance with standard operating procedures and customer or partner agreements.</li><li>Support and prepare investigations related to deviations and other quality events, ensuring issues are properly documented, thoroughly investigated, and justified.</li><li>Support continuous improvement initiatives by applying Lean Manufacturing principles, 5S, and other Lean tools to improve processes and eliminate waste.</li><li>Assist with writing deviations, investigations, and other quality documentation to support overall compliance with the companys quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in a scientific discipline or related field, or equivalent education and experience.</li><li>3+ years of quality experience in a cGMP manufacturing environment.</li><li>Strong knowledge of cGMP, GDP, and quality documentation requirements.</li><li>Hands-on experience with quality systems, including deviations, CAPAs, investigations, change controls, and batch record review.</li></ul>Work EnvironmentThis is a full-time QA Specialist position working a consistent daytime schedule with a typical start time between 7:00 AM and 9:00 AM. The role is fully onsite at a manufacturing facility and is primarily office-based, with your own cubicle and autonomy to manage your day and workload. The environment offers exposure to a diverse range of products, including beauty, bath and body items, lip balms, skincare, sunscreens, cleaning detergents, and other personal care and OTC products, providing broad manufacturing and quality experience.Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $26.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Eden Prairie, MN.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Eden Prairie,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

12 month contractDescription	Oversee internal quality operations and at external service providers (CDMOs/CTLs)	Review and approve service providers GMP documentation	Review and approve master/executed batch records, packaging records for, drug substances, drug product/finished drug product 	Perform GMP raw material release activities for internal manufacturing operations	Review and approve laboratory data related to release and stability of GMP materials, qualification of test methods and reference standards, including protocols, data and reports	Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents 	Review records including audit trails and ensure integrity of data and results generated by internal colleagues external CDMOs/CTLs	Support batch disposition activities, including data upload, review, and documentation in applicable quality systems	Compile data for Quality system reviewsAdditional Skills &amp; Qualifications	Bachelors in a scientific discipline with 4+ years of experience in the FDA regulated pharmaceutical/biotech industry with GMP manufacturing operations analytical development and quality 	Experience in Biologics and Combination Products (Cell and Gene Therapy, monoclonal antibodies) is preferred 	Experience with review of GMP manufacturing records (Master/Executed batch records, change controls, deviations, investigations, change controls, product complaints) associated with clinical programs	Hands-on experience with laboratory testing and method validationJob Type &amp; LocationThis is a Contract position based out of Lexington, MA.Pay and BenefitsThe pay range for this position is $60.00 - $70.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Lexington, MA.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Lexington,MA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Specilaist Quality Control

QA Supervisor - OvernightsBook here for more information: https://talentassistant.actalentservices.com/assistant/bookings/BfUTMTxlA growing food manufacturing organization is seeking a Food Safety &amp; Quality Assurance Supervisor to support and oversee quality and food safety programs within a production environment. This role will be responsible for supervising QA staff, ensuring compliance with regulatory and customer requirements, and supporting continuous improvement initiatives across operations. The position works closely with cross-functional teams including Operations, Sanitation, Maintenance, Warehousing, and Supply Chain to maintain high standards of food safety and product quality.Responsibilities<ul><li>Supervise and manage QA technicians and hourly quality staff.</li><li>Support onboarding, training, and ongoing development of QA personnel.</li><li>Allocate resources and manage workflows to meet departmental and operational goals.</li><li>Ensure effective food safety and quality training across cross-functional teams.</li><li>Support implementation and continuous improvement of food safety programs and regulatory compliance.</li><li>Oversee and verify adherence to HACCP, GMP, SSOP, and prerequisite programs.</li><li>Monitor production activities to ensure compliance with quality and food safety standards.</li><li>Analyze production and quality data to identify trends and improvement opportunities.</li><li>Review production records and perform pre-shipment checks to ensure only compliant products are released.</li><li>Lead investigations into customer complaints, non-conformances, deviations, and in-process quality issues.</li><li>Drive corrective and preventive actions (CAPA) and ensure proper documentation.</li><li>Partner with sanitation teams to verify cleaning effectiveness and identify improvement areas.</li><li>Generate shift reports and communicate findings across departments to ensure timely resolution.</li></ul>Essential Skills<ul><li>Quality assurance expertise in USDA and FDA standards.</li><li>Experience in food and beverage production.</li><li>Bilingual in Spanish.</li><li>Strong working knowledge of HACCP principles, GMPs, and sanitation programs.</li><li>Proficiency in food safety and quality systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in a scientific discipline or equivalent hands-on experience in food manufacturing quality.</li><li>35+ years of experience in food safety/quality within a USDA manufacturing environment.</li><li>Prior supervisory or team lead experience preferred.</li></ul>Work EnvironmentThe position covers two sites between Central Islip and Bayshore, owning all quality aspects for the shift. The majority of the day will be spent on the production floor with an office available. The supervisor will manage a department with six direct reports and collaborate closely with a sanitation team consisting of approximately 50 people on the overnight shift. The work shift is 10:00 pm to 6:30 am, 5-6 days a week as needed. Some team members only speak Spanish.Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Central Islip,NY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Supervisor - Overnights

Job Title: QA Supervisor - OvernightsJob DescriptionA growing food manufacturing organization is seeking a Food Safety &amp; Quality Assurance Supervisor to support and oversee quality and food safety programs within a production environment. This role will be responsible for supervising QA staff, ensuring compliance with regulatory and customer requirements, and supporting continuous improvement initiatives across operations. The position works closely with cross-functional teams including Operations, Sanitation, Maintenance, Warehousing, and Supply Chain to maintain high standards of food safety and product quality.Responsibilities<ul><li>Supervise and manage QA technicians and hourly quality staff.</li><li>Support onboarding, training, and ongoing development of QA personnel.</li><li>Allocate resources and manage workflows to meet departmental and operational goals.</li><li>Ensure effective food safety and quality training across cross-functional teams.</li><li>Support implementation and continuous improvement of food safety programs and regulatory compliance.</li><li>Oversee and verify adherence to HACCP, GMP, SSOP, and prerequisite programs.</li><li>Monitor production activities to ensure compliance with quality and food safety standards.</li><li>Analyze production and quality data to identify trends and improvement opportunities.</li><li>Review production records and perform pre-shipment checks to ensure only compliant products are released.</li><li>Lead investigations into customer complaints, non-conformances, deviations, and in-process quality issues.</li><li>Drive corrective and preventive actions (CAPA) and ensure proper documentation.</li><li>Partner with sanitation teams to verify cleaning effectiveness and identify improvement areas.</li><li>Generate shift reports and communicate findings across departments to ensure timely resolution.</li><li>Maintain strong communication with both internal teams and external stakeholders.</li><li>Support regulatory and third-party inspections as needed.</li><li>Collaborate with cross-functional teams to resolve quality and food safety issues.</li></ul>Essential Skills<ul><li>Quality assurance expertise in USDA and FDA standards.</li><li>Experience in food and beverage production.</li><li>Bilingual in Spanish.</li><li>Strong working knowledge of HACCP principles, GMPs, and sanitation programs.</li><li>Proficiency in food safety and quality systems.</li><li>HACCP certification strongly preferred; SQF certification is a plus.</li><li>Strong analytical, organizational, and problem-solving abilities.</li><li>Ability to communicate effectively across all levels of an organization.</li><li>Proficiency in Microsoft Office (Excel, Word, Outlook, etc.).</li><li>Ability to take initiative and proactively address food safety and quality concerns.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in a scientific discipline or equivalent hands-on experience in food manufacturing quality.</li><li>35+ years of experience in food safety/quality within a USDA manufacturing environment.</li><li>Prior supervisory or team lead experience preferred.</li></ul>Work EnvironmentThe position covers two sites between Central Islip and Bayshore, owning all quality aspects for the shift. The majority of the day will be spent on the production floor with an office available. The supervisor will manage a department with six direct reports and collaborate closely with a sanitation team consisting of approximately 50 people on the overnight shift. The work shift is 10:00 pm to 6:30 am, 5-6 days a week as needed. Some team members only speak Spanish.Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Central Islip,NY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QA Supervisor - OvernightsJob DescriptionA growing food manufacturing organization is seeking a Food Safety &amp; Quality Assurance Supervisor to support and oversee quality and food safety programs within a production environment. This role will be responsible for supervising QA staff, ensuring compliance with regulatory and customer requirements, and supporting continuous improvement initiatives across operations. The position works closely with cross-functional teams including Operations, Sanitation, Maintenance, Warehousing, and Supply Chain to maintain high standards of food safety and product quality.Responsibilities<ul><li>Supervise and manage QA technicians and hourly quality staff.</li><li>Support onboarding, training, and ongoing development of QA personnel.</li><li>Allocate resources and manage workflows to meet departmental and operational goals.</li><li>Ensure effective food safety and quality training across cross-functional teams.</li><li>Support implementation and continuous improvement of food safety programs and regulatory compliance.</li><li>Oversee and verify adherence to HACCP, GMP, SSOP, and prerequisite programs.</li><li>Monitor production activities to ensure compliance with quality and food safety standards.</li><li>Analyze production and quality data to identify trends and improvement opportunities.</li><li>Review production records and perform pre-shipment checks to ensure only compliant products are released.</li><li>Lead investigations into customer complaints, non-conformances, deviations, and in-process quality issues.</li><li>Drive corrective and preventive actions (CAPA) and ensure proper documentation.</li><li>Partner with sanitation teams to verify cleaning effectiveness and identify improvement areas.</li><li>Generate shift reports and communicate findings across departments to ensure timely resolution.</li><li>Maintain strong communication with both internal teams and external stakeholders.</li><li>Support regulatory and third-party inspections as needed.</li><li>Collaborate with cross-functional teams to resolve quality and food safety issues.</li></ul>Essential Skills<ul><li>Quality assurance expertise in USDA and FDA standards.</li><li>Experience in food and beverage production.</li><li>Bilingual in Spanish.</li><li>Strong working knowledge of HACCP principles, GMPs, and sanitation programs.</li><li>Proficiency in food safety and quality systems.</li><li>HACCP certification strongly preferred; SQF certification is a plus.</li><li>Strong analytical, organizational, and problem-solving abilities.</li><li>Ability to communicate effectively across all levels of an organization.</li><li>Proficiency in Microsoft Office (Excel, Word, Outlook, etc.).</li><li>Ability to take initiative and proactively address food safety and quality concerns.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelors degree in a scientific discipline or equivalent hands-on experience in food manufacturing quality.</li><li>35+ years of experience in food safety/quality within a USDA manufacturing environment.</li><li>Prior supervisory or team lead experience preferred.</li></ul>Work EnvironmentThe position covers two sites between Central Islip and Bayshore, owning all quality aspects for the shift. The majority of the day will be spent on the production floor with an office available. The supervisor will manage a department with six direct reports and collaborate closely with a sanitation team consisting of approximately 50 people on the overnight shift. The work shift is 10:00 pm to 6:30 am, 5-6 days a week as needed. Some team members only speak Spanish.Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Pay and BenefitsThe pay range for this position is $70000.00 - $80000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Central Islip, NY.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Central Islip,NY.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QA TechnicianJob DescriptionThe QA Technician supports a dynamic, fast-paced Chemical Analysis Division that provides innovative analytical solutions across industries such as pharmaceutical, food and beverage, environmental, mining, cement, metals, and academic and government sectors. This role helps the team meet daily production schedules and product quality goals by performing tests, inspections, and documentation to ensure products comply with established quality standards. The position requires strong communication, technical, and operational skills, as well as a collaborative approach to working with cross-functional teams.Responsibilities<ul><li>Perform a range of tests and inspections on raw materials, in-process samples, and finished products to verify compliance with established quality standards.</li><li>Collect and analyze data from quality control activities to identify trends, patterns, and potential quality issues.</li><li>Maintain accurate and up-to-date quality assurance documentation, including test records, inspection reports, and other relevant documents.</li><li>Communicate findings clearly and promptly to relevant team members to support timely decision-making and corrective actions.</li><li>Work closely with quality engineers, production personnel, and supervisors to address quality-related concerns and implement corrective and preventive actions.</li><li>Support the achievement of daily production schedules by ensuring quality checks are completed efficiently and accurately.</li><li>Follow established procedures and documentation practices to ensure consistency and compliance with cGMP requirements.</li><li>Demonstrate high ethical standards by consistently upholding and not compromising quality requirements.</li><li>Use appropriate personal protective equipment and follow chemical hygiene guidelines while performing all duties.</li><li>Handle materials safely, including occasionally lifting and manipulating items up to 50 pounds, and perform tasks that require standing, reaching, bending, stooping, and grasping throughout the shift.</li></ul>Essential Skills<ul><li>Minimum of 1 year of work experience in Quality Assurance, Quality Control, or a closely related field.</li><li>Experience working in a cGMP (current Good Manufacturing Practice) environment.</li><li>High school diploma or equivalent.</li><li>Demonstrated ability to follow established procedures and documentation requirements.</li><li>Strong communication skills to collaborate effectively with cross-functional teams.</li><li>Ability to collect, interpret, and analyze quality control data to identify trends and issues.</li><li>High ethical standards with a strong commitment to maintaining product quality and compliance.</li><li>Capability to occasionally lift up to 50 pounds unassisted.</li><li>Comfort with standing and moving for extended periods, including reaching, bending, stooping, and grasping.</li><li>Basic digital literacy to manage documentation and quality records accurately.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with quality control and quality assurance principles and practices.</li><li>Experience supporting production environments where adherence to schedules and quality goals is critical.</li><li>Ability to multitask and work effectively in a dynamic, fast-paced team setting.</li><li>Strong attention to detail when performing tests, inspections, and documentation.</li><li>Willingness to consistently use personal protective equipment and follow chemical hygiene practices.</li></ul>Work EnvironmentThis position is based at a plant facility in Oakwood Village, Ohio, within a Chemical Analysis Division that supports a broad range of industrial and scientific sectors. The work environment is dynamic and fast paced, with a strong emphasis on teamwork, multitasking, and clear communication across quality, production, and supervisory teams. The role involves working in a cGMP-compliant setting where adherence to procedures and documentation standards is essential. The position is categorized as contingent in the United States and may involve scheduling flexibility across Sunday through Saturday. The work requires regular standing and movement, including reaching, bending, stooping, and grasping, as well as occasional lifting and manipulation of materials up to 50 pounds unassisted. Personal Protective Equipment (PPE) is required, and employees must follow chemical hygiene practices to ensure a safe working environment.Job Type &amp; LocationThis is a Contract position based out of Bedford, Ohio.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Bedford, Ohio.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Bedford,Ohio.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA Technician

<h3>Quality Assurance Technician</h3>We are seeking an experienced Quality Assurance Inspector to support lot-release and manufacturing quality activities within a regulated medical device environment. This onsite role in San Diego will be responsible for ensuring commercial and clinical products meet established quality standards, documentation requirements, and product acceptance criteria.Responsibilities:<ul><li>Perform in-process and final product inspection and documentation review.</li><li>Review records for accuracy, completeness, signatures, dates, and adherence to Good Documentation Practices.</li><li>Ensure documentation complies with current Good Manufacturing Practices.</li><li>Conduct in-process manufacturing quality audits.</li><li>Support nonconforming material and NCMR activities.</li><li>Perform product inspection and testing for clinical products.</li><li>Review shipping documentation for order accuracy.</li><li>Generate reports and graphs using Microsoft Word and Excel.</li><li>Work cross-functionally with Quality, Manufacturing, Operations, Engineering, and R&amp;D.</li><li>Assist with training and help identify and resolve quality-related issues.</li></ul>Qualifications:<ul><li>High school diploma or equivalent required.</li><li>Approximately 2 to 3 years of relevant quality, inspection, or manufacturing experience preferred.</li><li>Experience with Good Documentation Practices and GMP.</li><li>Experience with quality inspection, manufacturing documentation, and quality processes.</li><li>Familiarity with NCMRs or nonconforming material processes.</li><li>Strong organizational skills and attention to detail.</li><li>Proficiency with Microsoft Word and Excel.</li><li>Ability to make sound decisions regarding quality issues and requirements.</li><li>Ability to distinguish between specified colors and pass an annual color vision test.</li></ul>Work Environment:This is an onsite, hands-on quality position supporting medical device manufacturing and lot release in San Diego. The role combines documentation review, quality auditing, product inspection, testing, and cross-functional collaboration. The schedule is approximately 8:00 AM to 4:30 PM, 40 hours per week, with possible overtime. The assignment is expected to last up to one year and may be extended.Job Type &amp; LocationThis is a Contract position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $23.00 - $27.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of San Diego, CA.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in San Diego,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h3>QA/QC Electrical Specialist | Data Center Construction</h3>Join a leading data center construction program in Wisconsin and play a key role in ensuring electrical systems are installed safely, accurately, and in compliance with project specifications. This position is ideal for electrical professionals with a strong eye for quality and experience in mission-critical, industrial, or commercial construction environments.<h3>Why Join Us?</h3><ul><li>Projects located throughout Southeastern Wisconsin</li><li>$178/day Per Diem for travelers living 50+ miles from the project site</li><li>Long-term opportunities on large-scale data center projects</li><li>Work alongside industry-leading construction and commissioning teams</li></ul><h3>Key Responsibilities</h3><ul><li>Inspect electrical installations to ensure compliance with NEC, NFPA, project specifications, and quality standards.</li><li>Review electrical drawings, one-line diagrams, and construction documents.</li><li>Identify deficiencies, track corrective actions, and help prevent rework.</li><li>Maintain inspection reports, testing records, quality logs, and turnover documentation.</li><li>Support commissioning activities and verify installation readiness.</li><li>Collaborate with project teams, subcontractors, vendors, and commissioning personnel.</li><li>Utilize Procore, Bluebeam, Autodesk Build/BIM360, and similar platforms to manage project documentation.</li></ul><h3>Qualifications</h3><ul><li>3+ years of electrical construction, QA/QC, or commissioning experience.</li><li>Ability to read and interpret electrical drawings, schematics, and one-line diagrams.</li><li>Strong knowledge of NEC and NFPA standards.</li><li>Excellent attention to detail and documentation skills.</li><li>Data center, industrial, semiconductor, or mission-critical project experience is preferred.</li></ul><h3>Preferred</h3><ul><li>QA/QC or commissioning experience on large-scale construction projects.</li><li>Experience with Procore, BIM360, Autodesk Build, or Bluebeam.</li><li>Electrical license, certification, or technical training is a plus.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Port Washington, WI.Pay and BenefitsThe pay range for this position is $75000.00 - $110000.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of Port Washington, WI.Application DeadlineThis position is anticipated to close on Nov 20, 2026.Workplace TypeThis is a fully onsite position in Port Washington,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QA/QC Electrical Specialist- Data Center

Job Title: QC ChemistJob DescriptionThe QC Chemist performs quality control testing on products and raw materials to ensure they meet established specifications and support safe, consistent manufacturing. This role offers the opportunity to work with a wide range of tests and instruments in a fast-paced laboratory environment, gaining broad hands-on experience in analytical and wet chemistry techniques. The position is ideal for someone motivated, eager to learn, and interested in growing their career in a production-focused chemical laboratory.Responsibilities<ul><li>Perform quality control analysis of finished products, raw materials, and special inter-department projects as needed.</li><li>Analyze test data and approve, reject, or adjust products and raw materials based on corporate quality control specifications.</li><li>Reexamine retained product samples when there is suspicion of defects or quality issues.</li><li>Collaborate closely with manufacturing personnel to support consistent product quality and resolve issues promptly.</li><li>Use everyday laboratory equipment and instruments, including performing titrations and measurements of viscosity and pH, as well as operating ICP, AA, and HPLC instruments as needed.</li><li>Work with Manufacturing and Purchasing teams to help maintain high quality standards for raw materials and raw material sources.</li><li>Maintain accurate and complete records of test results and enter data into computer systems in a timely manner.</li><li>Perform general laboratory housekeeping to maintain a clean, safe, and organized work area.</li><li>Carry out other general laboratory duties as assigned to support overall lab operations.</li></ul>Essential Skills<ul><li>Bachelors degree in Chemistry, or in Biology for candidates interested in production chemistry work.</li><li>At least 1 year of hands-on laboratory experience, which may include academic lab work, with exposure to titrations, pH testing, and viscosity measurements.</li><li>Demonstrated experience with wet chemistry techniques, including titration and routine solution preparation.</li><li>Basic computer skills, including the ability to use Word and Excel for data entry and documentation.</li><li>Ability to work effectively in a fast-paced environment and keep up with a high volume of testing and tasks.</li><li>Strong motivation and a proactive attitude toward learning and taking on responsibilities.</li><li>Ability to communicate clearly and work collaboratively with laboratory, manufacturing, and purchasing personnel.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with ICP, ICP-OES, AA, IFTR, or HPLC techniques gained in school or previous roles.</li><li>Prior experience in a quality control or production chemistry laboratory environment.</li><li>Interest in developing a long-term career in a chemical laboratory with opportunities for growth and advancement.</li><li>Strong interpersonal skills, with a collaborative and supportive approach to working with peers.</li><li>Comfort working with a broad product line and learning a large variety of tests and analytical methods.</li></ul>Work EnvironmentThis role is based in a newly built, clean, and modern quality control laboratory designed to support efficient and accurate testing. The standard schedule is Monday through Friday from 6:00 a.m. to 2:30 p.m., with occasional overtime and possible Saturday work as needed. The lab operates at a fast pace, and team members move quickly to keep up with testing demands while maintaining high quality standards. You will work with a wide range of laboratory instruments and methods, including titrations, viscosity and pH measurements, ICP, AA, and HPLC. The environment is collaborative and supportive, with colleagues who value communication, teamwork, and a willingness to help one another. Dress is typical for a chemical laboratory setting, with appropriate lab attire and safety gear used to support a safe and professional workplace.Job Type &amp; LocationThis is a Contract to Hire position based out of Ferndale, MI.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Ferndale, MI.Application DeadlineThis position is anticipated to close on Nov 10, 2026.Workplace TypeThis is a fully onsite position in Ferndale,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Chemist

The Quality Control Technician will inspect and test incoming raw materials and finished products, with a focus on disposables and electronic components, to ensure they meet all quality, regulatory, and internal standards. This role documents and manages non-conformances, supports process improvements, and follows established quality system regulations, ISO standards, and internal procedures while working closely with cross-functional teams in a regulated manufacturing environment.Responsibilities<ul><li>Inspect and test incoming raw materials related to disposables and electronics using appropriate inspection and measurement tools.</li><li>Perform visual, dimensional, and functional inspections of finished products to verify compliance with specifications and standards.</li><li>Review processes to ensure procedural compliance and recommend improvements to enhance product quality and inspection efficiency.</li><li>Identify key inspection points on components and products and select the proper tools and equipment to evaluate those points.</li><li>Conduct visual and dimensional testing such as leak, stress, and punch/pull tests using equipment including an Instron, micrometers, and calipers.</li><li>Perform inspections and process returned goods and materials (RGAs/RMAs), ensuring proper documentation and disposition.</li><li>Review inspection data and Device History Records (DHRs), including sterilization records, for accuracy and compliance with applicable standards.</li><li>Use recognized sampling plans to determine appropriate statistical sample sizes for inspections and tests.</li><li>Perform and review tests in accordance with Good Manufacturing Practice (GMP) protocol requirements.</li><li>Document and review inspection results in accordance with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP).</li><li>Generate non-conforming material reports (NCMRs) for products that do not meet test specifications and promptly notify the appropriate personnel.</li><li>Support and communicate the needs of the department and company to management in a clear and timely manner.</li><li>Assist engineering staff with process improvement initiatives, including first article inspections and qualification testing for products and components.</li><li>Work across all quality assurance areas, including incoming quality control (IQC), final inspection, and electronics inspection, as needed.</li><li>Understand, follow, and apply Quality System Regulations (QSR), ISO requirements, and internal company guidelines in daily activities.</li><li>Execute and maintain accurate documentation and records in the designated quality and/or ERP systems.</li><li>Troubleshoot basic quality issues related to incoming inspection, product performance, or test results and escalate when necessary.</li><li>Collaborate effectively with team members and other departments to resolve quality issues and support a strong quality culture.</li><li>Work overtime on Fridays when required to meet production and inspection demands.</li></ul>Essential Skills<ul><li>High school diploma or equivalent, with a minimum of 1 years of previous quality control experience.</li><li>Strong experience in dimensional inspection using calipers, micrometers, snap gauges, torque tools, and vision systems such as optical comparators and OGP Smart systems.</li><li>Proficiency in visual and dimensional testing, including leak, stress, and punch/pull tests using an Instron and other metrology equipment.</li><li>Ability to read and interpret engineering drawings, blueprints, product specifications, and procedures.</li><li>Experience with incoming inspection processes for raw materials and components.</li><li>Hands-on experience working with non-conformances and generating Non-Conforming Material Reports (NCMRs).</li><li>Experience reviewing and working with Device History Records (DHRs), including complete work order processes from start to finish.</li><li>Basic computer skills, including working knowledge of MS Excel and MS Access.</li><li>Ability to use or learn quality and ERP systems for documentation and record keeping.</li><li>Detail-oriented approach with strong organizational skills and the ability to complete tasks with minimal supervision.</li><li>Good written and oral communication skills, including the ability to read, write, and understand English.</li><li>Strong interpersonal skills and the ability to work effectively in a team environment with other departments and individuals.</li><li>Ability to perform troubleshooting on quality and inspection issues related to pneumatics, mechanical, and electrical testing.</li><li>Adaptability to changing environments and priorities while maintaining high quality standards.</li><li>Willingness and ability to work overtime on Fridays as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in a medical device or cleanroom manufacturing environment is highly desired.</li><li>Familiarity with Quality System Regulations (QSR), ISO standards, and Good Manufacturing Practices (GMP).</li><li>Experience documenting and reviewing inspection results in compliance with GMP and Good Documentation Practice (GDP).</li><li>Background in working with returned goods and materials (RGAs/RMAs) and associated documentation.</li><li>Experience supporting first article inspections and qualification testing for new or revised products.</li><li>A proactive, "go-getter" attitude with a strong commitment to quality and continuous improvement.</li><li>Ability to communicate departmental needs and quality concerns clearly to management and engineering teams.</li><li>Comfort working across multiple quality assurance areas, including incoming inspection, final inspection, and electronics inspection.</li></ul>Work EnvironmentThis role operates in a regulated manufacturing and quality assurance environment, potentially including cleanroom areas and spaces dedicated to medical device or electronic component inspection. The Quality Control Technician works primarily on-site using a variety of inspection and testing equipment such as calipers, micrometers, snap gauges, torque tools, optical comparators, OGP Smart systems, Instron machines, and other metrology and testing instruments for pneumatic, mechanical, and electrical testing. Work involves frequent interaction with engineering, production, and other quality team members in a collaborative, team-oriented setting. Standard work hours are Monday through Thursday from 7:00 a.m. to 5:30 p.m., with the ability and expectation to work overtime on Fridays when required to support production and inspection needs. The environment emphasizes adherence to QSR, ISO, GMP, and internal quality procedures, as well as accurate documentation in computer systems including MS Excel, MS Access, and ERP or quality documentation tools. Appropriate work attire is required to comply with safety, cleanliness, and, where applicable, cleanroom or controlled-environment protocols.Job Type &amp; LocationThis is a Contract to Hire position based out of Allen, TX.Pay and BenefitsThe pay range for this position is $23.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Allen, TX.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Allen,TX.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Inspector

Biochemist - QC SpecialistJob DescriptionThe QC Specialist leads day-to-day quality control laboratory activities, serving as the primary technical resource for technicians and other specialists. This role performs routine release testing, drives method development and validation efforts, and supports technical transfers to ensure robust and compliant analytical practices. The QC Specialist acts as a subject matter expert on key laboratory equipment, leads quality events and investigations, and partners with leadership to optimize processes and uphold a culture of safety, compliance, and continuous improvement.Responsibilities<ul><li>Direct the daily workload of QC Technicians and other Specialists, ensuring that quality control policies, procedures, and standards are consistently followed.</li><li>Serve as the primary point of contact for technical instruction, clarification, and troubleshooting for the QC team.</li><li>Perform regular release testing to support product and material disposition in accordance with established methods and specifications.</li><li>Lead and execute specialized development experiments, including method development, optimization, and improvement activities.</li><li>Participate in and, when appropriate, own method validation activities to ensure analytical methods are robust, reliable, and compliant.</li><li>Support and lead technical transfers of analytical methods, ensuring smooth implementation and proper documentation across laboratories or functions.</li><li>Regularly lead and own quality events such as deviations, laboratory investigations, and change activities, ensuring timely, thorough, and well-documented resolutions.</li><li>Review and approve documentation generated by QC Technicians and other Specialists, ensuring accuracy, completeness, and compliance with procedures.</li><li>Audit inventory management practices in the laboratory to ensure reagents and materials are properly controlled, labeled, and stored.</li><li>Ensure reagent and material qualifications are maintained, including monitoring expiration dates, qualification status, and usage.</li><li>Serve as a Subject Matter Expert (SME) for specialized laboratory equipment, providing guidance on proper use and troubleshooting.</li><li>Coordinate routine maintenance schedules and calibration activities for critical laboratory instruments to ensure readiness and compliance.</li><li>Ensure laboratory equipment and systems remain in a state of control and meet regulatory and internal quality expectations.</li><li>Partner with the QC Leader to identify obsolete or inefficient processes and propose improvements to enhance laboratory systems and workflows.</li><li>Anticipate potential problems in QC processes and proactively develop effective solutions to prevent issues and improve efficiency.</li><li>Participate in internal and external audit activities, representing QC operations and providing accurate and timely information to auditors.</li><li>Proactively prepare the laboratory space for inspections by identifying and addressing potential compliance gaps before audits occur.</li><li>Promote and personify core values of integrity, respect, and excellence in all interactions and decisions within the QC function.</li><li>Foster an environment of safety, compliance, and inclusion within the laboratory, encouraging collaboration and open communication.</li><li>Provide training, coaching, and informal leadership to colleagues, helping to build technical capability and a culture of continuous improvement.</li><li>Utilize laboratory software tools, including Empower software and other relevant systems, to document, analyze, and report QC data accurately.</li><li>Maintain meticulous laboratory records and documentation, ensuring traceability and adherence to data integrity principles.</li><li>Communicate effectively with cross-functional partners to share results, escalate issues, and support decision-making related to product quality.</li></ul>Essential Skills<ul><li>Minimum of 4+ years of relevant laboratory experience in a quality control or closely related analytical environment.</li><li>Bachelors Degree in Biochemistry, Biological Sciences, Pharmaceutical Sciences, or a closely related field, or an advanced degree (Masters or Ph.D.) in Biology, Chemistry, or an associated science with at least 2+ years of relevant experience.</li><li>Hands-on experience with HPLC (High Performance Liquid Chromatography) techniques in an analytical laboratory setting.</li><li>Hands-on experience with ELISA (Enzyme-Linked Immunosorbent Assay) techniques, including execution and troubleshooting.</li><li>Direct experience in analytical laboratory operations, including routine testing, documentation, and compliance with established procedures.</li><li>Experience in leadership or training roles within a laboratory environment, including guiding or mentoring other team members.</li><li>Strong verbal communication skills, with the ability to explain complex technical concepts clearly to diverse audiences.</li><li>Strong written communication skills, including the ability to generate clear, accurate, and compliant documentation and reports.</li><li>Strong interpersonal skills, with the ability to work effectively with and lead a diverse group of colleagues in a collaborative environment.</li><li>Proficient computer literacy, including use of laboratory-related software and standard office applications.</li><li>Demonstrated strong attention to detail, with a proven track record of accuracy, thoroughness, and data integrity.</li><li>Demonstrated ability to act as a leader of change, driving improvements and supporting process optimization in the laboratory.</li><li>Experience using Empower software for chromatography data acquisition, processing, and reporting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree (Masters or Ph.D.) in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.</li><li>Experience leading or owning deviations, laboratory investigations, and change activities in a regulated environment.</li><li>Experience in method development, validation, and technical transfer for analytical assays.</li><li>Experience acting as a Subject Matter Expert (SME) for specialized laboratory equipment.</li><li>Demonstrated ability to anticipate potential issues in QC processes and implement proactive solutions.</li><li>Experience preparing laboratories for internal or external audits and inspections.</li><li>Proven ability to foster a culture of safety, compliance, integrity, respect, and excellence within a team environment.</li></ul>Work EnvironmentThis role operates in a laboratory-based quality control environment on a day-shift schedule, Monday through Friday. Standard working hours are typically 8:00 a.m. to 5:00 p.m., with flexibility to work alternative schedules such as 7:00 a.m. to 4:00 p.m. or 9:00 a.m. to 6:00 p.m. as needed. The QC Specialist works as part of a collaborative team, alongside approximately 68 other professionals in similar roles, all in permanent positions. The laboratory uses advanced analytical technologies, including HPLC systems, ELISA platforms, and Empower software for chromatography data management. The environment emphasizes safety, compliance, and inclusion, with a strong focus on integrity, respect, and excellence in daily operations. Standard laboratory attire and appropriate personal protective equipment are required to ensure a safe and professional workspace.Job Type &amp; LocationThis is a Contract position based out of Elwood, KS.Pay and BenefitsThe pay range for this position is $31.25 - $40.86/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Elwood, KS.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Elwood,KS.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Lab Analyst

Job Title: QC Lab Associate Job DescriptionThe QC Lab Associate primarily supports QC Microbiology Laboratory operations at a pharmaceutical manufacturing facility in Round Lake, IL. This role focuses on biological testing for biologics and drugs throughout all stages of the manufacturing process, including incoming raw materials, in-process samples, finished products, and facility environmental and critical systems microbiological monitoring. The position is a first-shift role with flexible hours between 8:00 a.m. and 5:00 p.m., requires weekend and holiday work, and involves working in both Drug Delivery and Penicillin facilities.Responsibilities<ul><li>Conduct microbial analyses on raw materials, in-process samples, finished products, and samples collected from environmental monitoring programs within the manufacturing facility.</li><li>Perform routine facility environmental monitoring, including surfaces, air, particulate, and personnel monitoring, as well as critical systems monitoring such as water, clean steam, process compressed air, and nitrogen.</li><li>Prepare media and reagents used within the laboratory to support microbiological testing and routine laboratory operations.</li><li>Operate laboratory instrumentation, including particle counters, pH meters, SAS equipment, autoclaves, and computer systems such as LIMS, to collect, record, and manage data.</li><li>Monitor inventory of supplies, equipment, reagents, and media; order, receive, and stock supplies as necessary to ensure uninterrupted laboratory operations.</li><li>Maintain a clean, safe, and organized laboratory area and perform regular laboratory housekeeping activities in accordance with internal procedures and safety standards.</li><li>Conduct and document laboratory and nonconformance investigations, including data review, root cause analysis, impact assessment, and development of appropriate corrective and preventive actions.</li><li>Maintain data integrity and ensure compliance with standard operating procedures, FDA Quality System Regulations, and current Good Manufacturing Practice (cGMP) regulations.</li><li>Follow, understand, and comply with established procedures and policies related to cGMPs and safety requirements.</li><li>Contribute to other laboratory tasks and projects as assigned, supporting team objectives and continuous improvement initiatives.</li><li>Work in both Drug Delivery and Penicillin facilities as needed to support manufacturing and laboratory operations.</li></ul>Essential Skills<ul><li>Ability to perform all essential laboratory duties satisfactorily, including microbiological testing and documentation.</li><li>Must not be allergic to Penicillin, Cephalosporin, or their related products and minerals due to work in Penicillin facilities.</li><li>Knowledge in basic biology and microbiology principles, including aseptic technique.</li><li>Proficiency in Laboratory Information Management Systems (LIMS) for data entry, tracking, and reporting.</li><li>Ability to handle multiple tasks concurrently and complete them in a timely manner while maintaining accuracy.</li><li>Strong attention to detail, conscientious work habits, and high reading comprehension skills for reviewing data and documentation.</li><li>Ability to lift up to 50 pounds when required to handle laboratory supplies and equipment.</li><li>Capability to work independently and as part of a team in a laboratory and manufacturing environment.</li><li>Flexibility to work weekends and holidays as needed to support production and laboratory schedules.</li><li>Bachelors degree in microbiology or biological science.</li><li>Minimum of 2 years of experience in a laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of Good Laboratory Practice (GLP) principles and pharmaceutical aseptic processing cGMP requirements is preferred.</li><li>Demonstrated technical writing skills for documenting investigations, procedures, and reports.</li><li>Familiarity with structured root cause investigation methodologies, including DMAIC (Define, Measure, Analyze, Improve, Control).</li><li>Self-motivation, adaptability, and a positive attitude in a highly dynamic environment.</li><li>Strong organizational skills to manage inventory, documentation, and multiple ongoing tasks.</li><li>Ability to collaborate effectively with cross-functional teams in manufacturing and quality.</li><li>Comfort working in both Drug Delivery and Penicillin facilities and adapting to different process areas.</li></ul>Work EnvironmentThis is a first-shift position with hours typically between 8:00 a.m. and 5:00 p.m., operating on a Thursday through Monday schedule. Weekend and holiday work is required, and occasional off-shift work may be needed to support manufacturing and testing demands. The role is based in a QC Microbiology Laboratory within a pharmaceutical manufacturing facility in Round Lake, IL, and involves work in both Drug Delivery and Penicillin production areas. The environment includes routine exposure to biologics, drugs, and related materials, as well as critical systems such as purified water, clean steam, compressed air, and nitrogen. Laboratory work involves regular use of instrumentation such as particle counters, pH meters, SAS equipment, autoclaves, and computer systems including LIMS. The facility maintains strict cGMP, GLP, and FDA QSR standards, emphasizing data integrity, safety, and cleanliness. Showers are required when leaving the facility, and employees are expected to follow all safety procedures and dress appropriately for a controlled laboratory and manufacturing environment. The work requires standing for extended periods, handling laboratory materials, and occasionally lifting up to 50 pounds in a clean, highly regulated setting.Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Round Lake, IL.Application DeadlineThis position is anticipated to close on Nov 5, 2026.Workplace TypeThis is a fully onsite position in Round Lake,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Lab Associate

Job Title: QC Lab SupervisorJob DescriptionThe QC Supervisor oversees all quality control laboratory activities on 3rd shift (12:00 a.m. 8:00 a.m., Monday through Friday). This role manages laboratory operations, ensures accurate and compliant analytical testing, and provides technical support for routine processes and new products within a regulated GMP environment.Responsibilities<ul><li>Accept full responsibility for managing the quality control laboratory during the assigned shift.</li><li>Provide analytical support for routine processes and new product introductions in accordance with GMP requirements.</li><li>Manage the maintenance and calibration of laboratory equipment to ensure accurate and reliable performance.</li><li>Oversee documentation of raw materials, intermediates, in-process controls (IPCs), stability and cleaning samples, ensuring accuracy and compliance.</li><li>Review existing standard operating procedures (SOPs) and SOPQs and write new procedures as needed for new equipment, technologies, or processes.</li><li>Participate in the description and optimization of technical procedures and the review of analytical methods.</li><li>Initiate and manage change controls related to documentation, systems, and quality control laboratory reports.</li><li>Support the introduction and implementation of new work procedures in the laboratory.</li><li>Approve or reject raw materials, intermediates, in-process controls, stability samples, and cleaning samples based on analytical results and established criteria.</li><li>Ensure timely and accurate equipment maintenance and calibration activities are documented and completed.</li><li>Prepare and review analytical records in accordance with current SOPs and SOPQs for approval or rejection decisions.</li><li>Maintain order, cleanliness, and organization within the laboratory to support efficient and safe operations.</li><li>Oversee data entry and calculations in laboratory systems, ensuring accuracy and completeness, and generate analytical records and bulletins as required.</li><li>Control and manage the sample library, including proper storage, tracking, and retrieval of samples.</li><li>Write and investigate deviations, out-of-specification (OOS), out-of-trend (OOT), out-of-expectation (OOE) results, and other laboratory events, ensuring thorough documentation and follow-up.</li><li>Promote and ensure compliance with Health, Safety and Environment procedures, quality standards, GMP systems, and Data Integrity principles after receiving appropriate training.</li><li>Support and drive continuous improvement by identifying, defining, and implementing initiatives that increase efficiency and optimize the use of available resources.</li><li>Collaborate with laboratory leadership and other stakeholders to ensure alignment with organizational quality and operational goals.</li><li>Provide guidance and day-to-day leadership to a small team of analysts on 3rd shift, fostering a culture of quality, safety, and continuous improvement.</li></ul>Qualifications<ul><li>Degree in Sciences, preferably in Chemistry or Pharmacy.</li><li>Minimum of 3+ years of chemistry laboratory experience within a GMP environment (such as food, pharmaceutical, medical device, or chemical industries).</li><li>Strong knowledge of analytical chemistry principles and laboratory practices.</li><li>Hands-on experience with wet chemistry techniques.</li><li>Practical experience with high-performance liquid chromatography (HPLC).</li><li>Experience with gas chromatography (GC) and related chromatographic techniques.</li><li>Understanding of GMP regulations and quality systems in a regulated environment.</li><li>Experience working with raw materials, intermediates, in-process controls (IPCs), stability samples, and cleaning samples, including approvals and rejections.</li><li>Familiarity with data review and data integrity requirements, including ALCOA and ALCOA+ principles and audit trail review.</li><li>Training in Health, Safety and Environment practices applicable to laboratory operations.</li><li>Training on analytical techniques such as HPLC, HRGC, GC, FTIR, and related methods.</li><li>Proficiency with Microsoft Office applications, particularly Excel and Word.</li><li>Ability to write, review, and implement SOPs and other controlled documentation.</li><li>Experience investigating deviations, OOS, OOT, OOE, and laboratory events and documenting findings clearly.</li><li>Strong attention to detail, organizational skills, and ability to manage multiple tasks in a fast-paced environment.</li><li>Ability to work independently on a night shift while providing guidance to other analysts.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Morton Grove, IL.Pay and BenefitsThe pay range for this position is $34.00 - $40.87/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Morton Grove, IL.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Morton Grove,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Lab Supervisor

Job Title: QC Lab TechnicianJob DescriptionThis position is responsible for providing laboratory support, preparing solutions and buffers used in QC testing, and performing measurements utilizing QC instrumentation. Additional responsibilities include instrument operation and calibration, cleaning, inventory management, and general lab and administrative duties. The role requires the ability to work independently as well as collaboratively within a team environment.Responsibilities<ul><li>Prepare buffers and reagents used in QC testing.</li><li>Submit pipettes for calibration.</li><li>Perform cleaning tasks, including mopping walk-in coolers and preparing cleaning solutions.</li><li>Conduct measurements using laboratory equipment such as a pH meter, scale, and NanoDrop for concentration measurements.</li><li>Perform dilutions, initiate instruments, acquire and save data, and change staining solutions.</li><li>Maintain cleaning and temperature logs in the lab.</li><li>Handle biohazard disposal.</li><li>Conduct raw material checks.</li></ul>Essential Skills<ul><li>Proficiency in laboratory techniques and quality control processes.</li><li>Strong attention to detail, verified by references.</li><li>3+ months of pipetting experience, which can include academic experience.</li><li>Willingness to work overtime as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in science is preferred but candidates with relevant coursework or lab experience will also be considered.</li></ul>Work EnvironmentThe position operates in a lab environment, working Monday through Friday on the first shift. Employees can start between 6 AM and 9 AM, working an 8-hour shift with a 30-minute meal break. Once the start time is determined, it should remain consistent. There may be some overtime required. This role is initially a 6-month contract with the potential for transitioning into a full-time position.Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $25.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Minneapolis,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Lab Technician

<h2 style="text-align:center;">QC Lab Technician</h2>Job DescriptionThis position is responsible for providing laboratory support, preparing solutions and buffers used in QC testing, and performing measurements utilizing QC instrumentation. Additional responsibilities include instrument operation and calibration, cleaning, inventory management, and general lab and administrative duties. The role requires the ability to work independently as well as collaboratively within a team environment.Responsibilities<ul><li>Prepare buffers and reagents used in QC testing.</li><li>Submit pipettes for calibration.</li><li>Perform cleaning tasks, including mopping walk-in coolers and preparing cleaning solutions.</li><li>Conduct measurements using laboratory equipment such as a pH meter, scale, and NanoDrop for concentration measurements.</li><li>Perform dilutions, initiate instruments, acquire and save data, and change staining solutions.</li><li>Maintain cleaning and temperature logs in the lab.</li><li>Handle biohazard disposal.</li><li>Conduct raw material checks.</li></ul>Essential Skills<ul><li>Proficiency in laboratory techniques and quality control processes.</li><li>Strong attention to detail, verified by references.</li><li>3+ months of pipetting experience, which can include academic experience.</li><li>Willingness to work overtime as needed.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in science is preferred but candidates with relevant coursework or lab experience will also be considered.</li></ul>Work EnvironmentThe position operates in a lab environment, working Monday through Friday on the first shift. Employees can start between 6 AM and 9 AM, working an 8-hour shift with a 30-minute meal break. Once the start time is determined, it should remain consistent. There may be some overtime required. This role is initially a 6-month contract with the potential for transitioning into a full-time position.Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $25.00 - $26.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Minneapolis, MN.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Minneapolis,MN.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

<h3>QC Laboratory Lead</h3><h4>Position Overview</h4>We are seeking an experienced QC Laboratory Lead to oversee daily operations within a GMP-regulated Quality Control laboratory. This individual will serve as the technical and operational leader for their shift, ensuring testing activities are executed safely, efficiently, and in alignment with manufacturing and product release timelines.This role is ideal for a strong analytical chemist who has transitioned into leadership and enjoys coordinating laboratory operations, managing priorities, mentoring analysts, and driving performance within a fast-paced pharmaceutical environment. Approximately 80% of the role is focused on laboratory leadership and operations management, with 20% dedicated to hands-on laboratory support and technical guidance.<h3>Key Responsibilities</h3><ul><li>Lead day-to-day operations of a GMP Quality Control laboratory supporting commercial manufacturing.</li><li>Build and maintain testing schedules up to two weeks in advance to support production and release timelines.</li><li>Coordinate daily workload and testing priorities for QC Analysts, Chemists, and Laboratory Operators.</li><li>Monitor laboratory performance metrics and ensure adherence to schedule-driven KPIs.</li><li>Serve as the primary point of contact for shift activities, issue resolution, and cross-functional communication.</li><li>Partner closely with Quality Assurance, Manufacturing, and external contract laboratories to ensure timely execution of testing activities.</li><li>Review analytical data and quality documentation to ensure compliance with GMP standards.</li><li>Provide technical mentorship, coaching, and guidance to laboratory personnel.</li><li>Support employee development through training, performance feedback, and knowledge sharing.</li><li>Approve employee timecards and assist with staffing and resource planning.</li><li>Escalate operational issues and drive solutions to maintain testing schedules and production commitments.</li></ul><h3>Required Qualifications</h3><ul><li>Bachelor's degree in Chemistry, Biochemistry, or a related Life Sciences discipline.</li><li>4+ years of Quality Control laboratory experience in a GMP-regulated environment.</li><li>1+ year of experience leading analysts, coordinating laboratory operations, or serving as a technical lead.</li><li>Strong knowledge of cGMP regulations, quality systems, SOP compliance, and data integrity requirements.</li><li>Hands-on experience with HPLC analysis.</li><li>Experience with additional analytical techniques such as:<ul><li>Gas Chromatography (GC)</li><li>Mass Spectrometry (MS)</li><li>Moisture Analysis</li><li>Method Validation and Validation Support Activities</li></ul></li><li>Proven ability to prioritize multiple projects and manage competing testing demands.</li></ul><h3>Preferred Qualifications</h3><ul><li>Experience supporting pharmaceutical, biotechnology, or regulated manufacturing operations.</li><li>Experience working with outsourced or contract testing laboratories.</li><li>Strong troubleshooting and problem-solving skills.</li><li>Ability to influence teams and drive results without direct authority.</li><li>Experience reviewing analytical data packages, deviations, investigations, and laboratory documentation.</li><li>Demonstrated success coaching, mentoring, and developing junior scientists and analysts.</li></ul><h3>Ideal Candidate Profile</h3>The ideal candidate combines strong analytical chemistry expertise with proven frontline leadership experience. They are highly organized, thrive in a fast-paced GMP environment, and excel at coordinating laboratory resources, balancing testing priorities, and ensuring on-time delivery of quality results that support manufacturing operations.<h3>Work Environment</h3><ul><li>Onsite role within a GMP-regulated pharmaceutical manufacturing facility.</li><li>Fast-paced Quality Control laboratory supporting commercial production.</li><li>Frequent collaboration with QC, QA, Manufacturing, Operations, and site leadership teams.</li><li>May require occasional overtime, evening, or weekend support based on production demands.</li><li>Laboratory PPE, gowning, and safety requirements apply.</li><li>Combination of laboratory work, documentation review, team leadership, and computer-based tasks.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $33.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Permanent position based out of San Diego, CA.Application DeadlineThis position is anticipated to close on Nov 4, 2026.Workplace TypeThis is a fully onsite position in San Diego,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Laboratory Lead

Job Title: Quality Control Sample Runner Food ManufacturingJob DescriptionThis role focuses on supporting the Quality Control (QC) team by collecting production samples and transporting them to the QC area within a food manufacturing facility. You will move between production floors and the QC department throughout your shift, navigating multiple flights of stairs while handling sample bags. This is a hands-on, physically active position that offers an opportunity to gain experience in a Quality Control operation in a large-scale food manufacturing environment.Responsibilities<ul><li>Collect production samples from designated areas on the manufacturing floor throughout the assigned shift.</li><li>Transport samples from downstairs production areas to the upstairs QC area in a timely and reliable manner.</li><li>Navigate approximately four flights of stairs repeatedly while performing sample collection and delivery duties.</li><li>Handle and carry approximately 710 sample bags per trip, with each sample weighing around 500 grams.</li><li>Deliver all collected samples to QC technicians promptly to support ongoing testing and quality checks.</li><li>Assist QC technicians with sample-related support activities as needed, excluding laboratory testing.</li><li>Work safely and follow all safety procedures within an active food manufacturing environment.</li><li>Maintain consistent, reliable attendance for the assigned shift, recognizing that one worker supports each shift.</li><li>Coordinate movement between production/sample collection areas and the QC department as operational needs require.</li><li>Adhere to all site policies, including hygiene and safety requirements specific to food manufacturing.</li></ul>Qualifications<ul><li>High School Diploma</li></ul>Job Type &amp; LocationThis is a Contract position based out of Chicago, IL.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Chicago, IL.Application DeadlineThis position is anticipated to close on Nov 23, 2026.Workplace TypeThis is a fully onsite position in Chicago,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Sample Runner

Job Title: QC Scientist IJob DescriptionWe are seeking a QC Scientist I to perform routine testing of finished pharmaceutical products and stability samples. The role involves conducting HPLC and wet chemistry analysis following validated methods and SOPs, preparing standards, reagents, diluents, and mobile phases, and documenting testing activities and results accurately in laboratory systems.Responsibilities<ul><li>Conduct routine testing of finished pharmaceutical products and stability samples.</li><li>Perform HPLC and wet chemistry analysis following validated methods and SOPs.</li><li>Prepare standards, reagents, diluents, and mobile phases.</li><li>Document testing activities and results accurately in laboratory systems.</li><li>Perform instrument calibration, verification, and routine maintenance.</li><li>Identify and communicate out-of-specification or unexpected results.</li><li>Maintain compliance with GMP, GLP, safety, and documentation requirements.</li><li>Support manufacturing and quality operations through timely laboratory testing.</li></ul>Essential Skills<ul><li>Bachelor's degree in Chemistry or related physical science.</li><li>1-2 years of laboratory experience.</li><li>Hands-on HPLC experience.</li><li>Experience conducting analytical testing in a regulated environment.</li><li>Strong documentation and technical writing skills.</li><li>Ability to work independently and manage multiple priorities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Pharmaceutical industry experience.</li><li>Experience with GMP and GLP environments.</li><li>Experience with dissolution testing, chromatography, or stability testing.</li><li>Familiarity with laboratory investigations and OOS procedures.</li><li>Experience using LIMS or laboratory documentation systems.</li></ul>Work EnvironmentThe role operates on a stable Monday-Friday first-shift schedule with a flexible start time between 6:00 AM and 9:00 AM. The schedule must remain consistent once established. The work environment offers a collaborative laboratory team with structured processes and support, providing exposure to industry-leading analytical technologies and laboratory practices. This is an excellent opportunity for early-career scientists looking to gain experience in a highly regulated pharmaceutical environment, with strong training, development, and advancement opportunities.Job Type &amp; LocationThis is a Contract position based out of Cincinnati, OH.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Cincinnati, OH.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Cincinnati,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Scientist I

We are hiring for a QC Chemist I in the Pharmaceutical industry here in the Columbus, Ohio area. This is a long-term career opportunity for someone looking to grow in the sciences.This role will primarily be performing Quality Control laboratory testing on generic pharmaceutical products. An ideal candidate for this role will have a Bachelors Degree in a scientific field with strong chemistry experience from school.Shift: M-F 3pm-11:30pm (after training you can work 4 days a week, 10 hour shifts) INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO JABRUNNER @ACTALENTSERVICES .COM OR TEXT JAKE AT 614. 726. 7399 TO SET UP AN IMMEDIATE PHONE INTERVIEW!Job Description:This role will primarily be performing quality control laboratory testing on generic pharmaceutical products. Testing will primarily be chemistry focused and job duties will include:<ul><li>You will be performing sample preparation, wet chemistry, standard weighing, dilutions, and High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC).</li><li>Testing will be on a variety of generic pharmaceutical products including Oral Dose Solids and Nasals.</li><li>Will perform a variety of highly regulated documentation activities.</li><li>Will perform other duties in the lab as assigned.</li></ul>Qualifications:<ul><li>Bachelor's degree in a science field with strong chemistry coursework</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Columbus,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Scientist IJob DescriptionThe QC Scientist I performs analytical and quality control testing in a regulated laboratory environment. In this role, you execute established analytical methods, analyze and document results, maintain laboratory equipment, and ensure all laboratory activities comply with cGMP, GLP, GDP, and applicable quality requirements. You work independently with a strong scientific foundation in analytical chemistry, biochemistry, biology, or a related discipline, demonstrating exceptional attention to detail and the ability to troubleshoot analytical and laboratory issues within established quality systems.Responsibilities<ul><li>Perform routine and non-routine quality control testing using established analytical methods and instrumentation.</li><li>Prepare samples, reagents, standards, and solutions according to defined procedures.</li><li>Conduct testing using techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption-based methods, dissolution testing, and general organic chemistry techniques.</li><li>Analyze and interpret laboratory results, ensuring accuracy and reliability of data.</li><li>Identify unexpected results or testing issues and promptly escalate or investigate as appropriate.</li><li>Execute all laboratory activities in accordance with cGMP, GLP, GDP, SOPs, and established quality management systems.</li><li>Maintain complete, accurate, and traceable laboratory records that meet data integrity and documentation review requirements.</li><li>Follow applicable pharmacopeia standards and regulatory requirements during testing and documentation.</li><li>Support laboratory investigations, deviations, and corrective actions when required.</li><li>Support microbiological testing activities as needed, following proper procedures and protocols.</li><li>Utilize proper aseptic technique when handling samples and materials to prevent contamination.</li><li>Follow contamination-control practices and laboratory safety procedures at all times.</li><li>Operate, maintain, and calibrate laboratory instrumentation to ensure optimal performance.</li><li>Perform routine troubleshooting on laboratory instruments to resolve performance issues.</li><li>Document equipment maintenance and calibration activities in accordance with quality and regulatory expectations.</li><li>Use LIMS and analytical software to enter, track, review, and report laboratory data.</li><li>Maintain an organized laboratory environment and comply with PPE and safety requirements.</li></ul>Essential Skills<ul><li>Minimum 2 years of experience in a quality control laboratory environment.</li><li>Strong understanding of cGMP, GLP, GDP, and quality management systems.</li><li>Hands-on experience with analytical laboratory instrumentation and testing techniques.</li><li>Ability to execute testing according to established SOPs and accurately document results.</li><li>Experience maintaining, calibrating, and troubleshooting laboratory equipment.</li><li>Bachelors degree in a scientific discipline, preferably chemistry, biochemistry, biology, molecular biology, or a related field.</li><li>Experience following SOPs and GDP documentation practices.</li><li>Hands-on analytical laboratory experience in a regulated environment.</li><li>Strong computer skills, including proficiency with Microsoft Office and laboratory software.</li><li>Strong analytical and problem-solving abilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Biotechnology or pharmaceutical quality control experience.</li><li>Experience with HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, and dissolution testing.</li><li>Microbiological testing experience and familiarity with aseptic technique.</li><li>Experience using LIMS to manage and review laboratory data.</li><li>Knowledge of pharmacopeia standards and applicable regulatory requirements.</li></ul>Work EnvironmentThis role is based in a regulated laboratory environment that emphasizes compliance with cGMP, GLP, GDP, and established quality systems. You work with a variety of analytical instruments and technologies, including HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, dissolution testing equipment, and general organic chemistry tools, as well as LIMS and other analytical software. The laboratory follows strict contamination-control and safety procedures, and appropriate PPE is required. The position offers a comprehensive benefits package, including paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, a health savings account, life insurance, short-term and long-term disability, an employee assistance program, and transportation benefits, supporting a stable and well-rounded work experience.Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Pay and BenefitsThe pay range for this position is $26.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully onsite position in Eugene,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Scientist IMUST HAVE<ul><li>Biotechnology or pharmaceutical quality control experience.</li><li>Experience with HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, and dissolution testing.</li><li>Microbiological testing experience and familiarity with aseptic technique.</li><li>Experience using LIMS to manage and review laboratory data.</li><li>Knowledge of pharmacopeia standards and applicable regulatory requirements.</li></ul>Job DescriptionThe QC Scientist I performs analytical and quality control testing in a regulated laboratory environment. In this role, you execute established analytical methods, analyze and document results, maintain laboratory equipment, and ensure all laboratory activities comply with cGMP, GLP, GDP, and applicable quality requirements. You work independently with a strong scientific foundation in analytical chemistry, biochemistry, biology, or a related discipline, demonstrating exceptional attention to detail and the ability to troubleshoot analytical and laboratory issues within established quality systems.Responsibilities<ul><li>Perform routine and non-routine quality control testing using established analytical methods and instrumentation.</li><li>Prepare samples, reagents, standards, and solutions according to defined procedures.</li><li>Conduct testing using techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption-based methods, dissolution testing, and general organic chemistry techniques.</li><li>Analyze and interpret laboratory results, ensuring accuracy and reliability of data.</li><li>Identify unexpected results or testing issues and promptly escalate or investigate as appropriate.</li><li>Execute all laboratory activities in accordance with cGMP, GLP, GDP, SOPs, and established quality management systems.</li><li>Maintain complete, accurate, and traceable laboratory records that meet data integrity and documentation review requirements.</li><li>Follow applicable pharmacopeia standards and regulatory requirements during testing and documentation.</li><li>Support laboratory investigations, deviations, and corrective actions when required.</li><li>Support microbiological testing activities as needed, following proper procedures and protocols.</li><li>Utilize proper aseptic technique when handling samples and materials to prevent contamination.</li><li>Follow contamination-control practices and laboratory safety procedures at all times.</li><li>Operate, maintain, and calibrate laboratory instrumentation to ensure optimal performance.</li><li>Perform routine troubleshooting on laboratory instruments to resolve performance issues.</li><li>Document equipment maintenance and calibration activities in accordance with quality and regulatory expectations.</li><li>Use LIMS and analytical software to enter, track, review, and report laboratory data.</li><li>Maintain an organized laboratory environment and comply with PPE and safety requirements.</li></ul>Essential Skills<ul><li>Minimum 2 years of experience in a quality control laboratory environment.</li><li>Strong understanding of cGMP, GLP, GDP, and quality management systems.</li><li>Hands-on experience with analytical laboratory instrumentation and testing techniques.</li><li>Ability to execute testing according to established SOPs and accurately document results.</li><li>Experience maintaining, calibrating, and troubleshooting laboratory equipment.</li><li>Bachelors degree in a scientific discipline, preferably chemistry, biochemistry, biology, molecular biology, or a related field.</li><li>Experience following SOPs and GDP documentation practices.</li><li>Hands-on analytical laboratory experience in a regulated environment.</li><li>Strong computer skills, including proficiency with Microsoft Office and laboratory software.</li><li>Strong analytical and problem-solving abilities</li></ul>Work EnvironmentThis role is based in a regulated laboratory environment that emphasizes compliance with cGMP, GLP, GDP, and established quality systems. You work with a variety of analytical instruments and technologies, including HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, dissolution testing equipment, and general organic chemistry tools, as well as LIMS and other analytical software. The laboratory follows strict contamination-control and safety procedures, and appropriate PPE is required. The position offers a comprehensive benefits package, including paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, a health savings account, life insurance, short-term and long-term disability, an employee assistance program, and transportation benefits, supporting a stable and well-rounded work experience.Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Pay and BenefitsThe pay range for this position is $26.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Application DeadlineThis position is anticipated to close on Nov 12, 2026.Workplace TypeThis is a fully onsite position in Eugene,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Scientist IJob DescriptionWe are seeking a QC Scientist I to perform routine testing of finished pharmaceutical products and stability samples. The role involves conducting HPLC and wet chemistry analysis following validated methods and SOPs, preparing standards, reagents, diluents, and mobile phases, and documenting testing activities and results accurately in laboratory systems.Responsibilities<ul><li>Conduct routine testing of finished pharmaceutical products and stability samples.</li><li>Perform HPLC and wet chemistry analysis following validated methods and SOPs.</li><li>Prepare standards, reagents, diluents, and mobile phases.</li><li>Document testing activities and results accurately in laboratory systems.</li><li>Perform instrument calibration, verification, and routine maintenance.</li><li>Identify and communicate out-of-specification or unexpected results.</li><li>Maintain compliance with GMP, GLP, safety, and documentation requirements.</li><li>Support manufacturing and quality operations through timely laboratory testing.</li></ul>Essential Skills<ul><li>Bachelor's degree in Chemistry or related physical science.</li><li>1-2 years of laboratory experience.</li><li>Hands-on HPLC experience.</li><li>Experience conducting analytical testing in a regulated environment.</li><li>Strong documentation and technical writing skills.</li><li>Ability to work independently and manage multiple priorities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Pharmaceutical industry experience.</li><li>Experience with GMP and GLP environments.</li><li>Experience with dissolution testing, chromatography, or stability testing.</li><li>Familiarity with laboratory investigations and OOS procedures.</li><li>Experience using LIMS or laboratory documentation systems.</li></ul>Work EnvironmentThe role operates on a stable Monday-Friday first-shift schedule with a flexible start time between 6:00 AM and 9:00 AM. The schedule must remain consistent once established. The work environment offers a collaborative laboratory team with structured processes and support, providing exposure to industry-leading analytical technologies and laboratory practices. This is an excellent opportunity for early-career scientists looking to gain experience in a highly regulated pharmaceutical environment, with strong training, development, and advancement opportunities.Job Type &amp; LocationThis is a Contract position based out of Cincinnati, OH.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Cincinnati, OH.Application DeadlineThis position is anticipated to close on Nov 3, 2026.Workplace TypeThis is a fully onsite position in Cincinnati,OH.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Scientist IJob DescriptionThe QC Scientist I supports quality control activities in a laboratory environment by performing analytical testing, maintaining laboratory instruments, and ensuring compliance with regulatory and quality standards. This role applies scientific knowledge and hands-on laboratory skills to generate accurate, reliable data that supports product quality, process control, and regulatory submissions. The QC Scientist I follows established procedures, documents all work in accordance with Good Documentation Practices, and contributes to a culture of continuous improvement and operational excellence.Responsibilities<ul><li>Perform routine and non-routine quality control testing in accordance with established standard operating procedures (SOPs) and applicable regulatory guidelines.</li><li>Apply a strong understanding of cGMP, GLP, GDP, and quality management systems to ensure all testing and documentation meet compliance requirements.</li><li>Execute analytical methods using laboratory instrumentation such as HPLC, ICP-MS, UV-Vis spectroscopy, NMR, flow cytometry, and dissolution testing equipment, as applicable to assigned projects.</li><li>Conduct microbiological testing and aseptic techniques where required, ensuring strict adherence to contamination control practices.</li><li>Accurately document all testing activities, observations, calculations, and results in laboratory notebooks, electronic systems, and LIMS in accordance with Good Documentation Practices.</li><li>Review data for accuracy, completeness, and consistency, and promptly report any deviations, out-of-specification results, or anomalies to appropriate personnel.</li><li>Perform routine maintenance, calibration, and basic troubleshooting of laboratory equipment to ensure instruments remain in a qualified and reliable state.</li><li>Follow established schedules and priorities to complete testing within required timelines, supporting batch release, stability studies, and method validation as needed.</li><li>Interpret analytical data, apply strong analytical and problem-solving skills to investigate issues, and contribute to root cause analysis and corrective actions.</li><li>Collaborate with colleagues in quality, manufacturing, and other scientific teams to support cross-functional projects and ensure alignment with quality objectives.</li><li>Participate in training on new methods, instruments, and quality procedures, and apply this knowledge to daily work.</li><li>Support continuous improvement initiatives by identifying opportunities to enhance laboratory workflows, documentation practices, and data integrity.</li><li>Ensure laboratory activities align with pharmacopeia standards and relevant regulatory requirements where applicable.</li></ul>Essential Skills<ul><li>Bachelor's degree in Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific discipline.</li><li>Minimum 2 years of experience in a quality control laboratory environment.</li><li>Strong understanding of current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and quality management systems.</li><li>Hands-on analytical laboratory experience with instrumentation and testing techniques.</li><li>Experience maintaining, calibrating, and troubleshooting laboratory equipment.</li><li>Ability to execute testing according to established SOPs and accurately document results.</li><li>Strong computer skills, including proficiency with Microsoft Office and laboratory software.</li><li>Strong analytical and problem-solving abilities.</li><li>Ability to follow detailed procedures and work with a high level of accuracy and attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Biotechnology or pharmaceutical quality control experience.</li><li>Experience with high-performance liquid chromatography (HPLC).</li><li>Experience with inductively coupled plasma mass spectrometry (ICP-MS).</li><li>Experience with UV-Vis spectroscopy.</li><li>Experience with flow cytometry.</li><li>Experience with nuclear magnetic resonance (NMR).</li><li>Experience with dissolution testing.</li><li>Experience with microbiological testing and aseptic technique.</li><li>Experience working with Laboratory Information Management Systems (LIMS).</li><li>Knowledge of pharmacopeia standards and relevant regulatory requirements.</li><li>Interest in continuous learning and professional development in quality control and analytical sciences.</li></ul>Work EnvironmentThis position is based in a quality control laboratory environment that emphasizes compliance, accuracy, and safety. The role involves extensive hands-on work with analytical instruments and laboratory equipment, including technologies such as HPLC, ICP-MS, UV-Vis spectroscopy, NMR, flow cytometry, dissolution testers, and microbiological testing systems. Work is performed in accordance with cGMP, GLP, GDP, and quality management system requirements, with a strong focus on data integrity and documentation. The environment is collaborative and team-oriented, with regular interaction with other scientists and quality professionals. Employees receive a comprehensive benefits package that typically includes paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, a health savings account, life insurance, short-term and long-term disability coverage, an employee assistance program, and transportation-related benefits. The laboratory setting may require the use of appropriate personal protective equipment and adherence to established safety and cleanliness standards.Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Pay and BenefitsThe pay range for this position is $29.90 - $34.50/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Application DeadlineThis position is anticipated to close on Nov 18, 2026.Workplace TypeThis is a fully onsite position in Eugene,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Scientist IMUST HAVE<ul><li>Biotechnology or pharmaceutical quality control experience.</li><li>Experience with HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, and dissolution testing.</li><li>Microbiological testing experience and familiarity with aseptic technique.</li><li>Experience using LIMS to manage and review laboratory data.</li><li>Knowledge of pharmacopeia standards and applicable regulatory requirements.</li></ul>Job DescriptionThe QC Scientist I performs analytical and quality control testing in a regulated laboratory environment. In this role, you execute established analytical methods, analyze and document results, maintain laboratory equipment, and ensure all laboratory activities comply with cGMP, GLP, GDP, and applicable quality requirements. You work independently with a strong scientific foundation in analytical chemistry, biochemistry, biology, or a related discipline, demonstrating exceptional attention to detail and the ability to troubleshoot analytical and laboratory issues within established quality systems.Responsibilities<ul><li>Perform routine and non-routine quality control testing using established analytical methods and instrumentation.</li><li>Prepare samples, reagents, standards, and solutions according to defined procedures.</li><li>Conduct testing using techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, absorption-based methods, dissolution testing, and general organic chemistry techniques.</li><li>Analyze and interpret laboratory results, ensuring accuracy and reliability of data.</li><li>Identify unexpected results or testing issues and promptly escalate or investigate as appropriate.</li><li>Execute all laboratory activities in accordance with cGMP, GLP, GDP, SOPs, and established quality management systems.</li><li>Maintain complete, accurate, and traceable laboratory records that meet data integrity and documentation review requirements.</li><li>Follow applicable pharmacopeia standards and regulatory requirements during testing and documentation.</li><li>Support laboratory investigations, deviations, and corrective actions when required.</li><li>Support microbiological testing activities as needed, following proper procedures and protocols.</li><li>Utilize proper aseptic technique when handling samples and materials to prevent contamination.</li><li>Follow contamination-control practices and laboratory safety procedures at all times.</li><li>Operate, maintain, and calibrate laboratory instrumentation to ensure optimal performance.</li><li>Perform routine troubleshooting on laboratory instruments to resolve performance issues.</li><li>Document equipment maintenance and calibration activities in accordance with quality and regulatory expectations.</li><li>Use LIMS and analytical software to enter, track, review, and report laboratory data.</li><li>Maintain an organized laboratory environment and comply with PPE and safety requirements.</li></ul>Essential Skills<ul><li>Minimum 2 years of experience in a quality control laboratory environment.</li><li>Strong understanding of cGMP, GLP, GDP, and quality management systems.</li><li>Hands-on experience with analytical laboratory instrumentation and testing techniques.</li><li>Ability to execute testing according to established SOPs and accurately document results.</li><li>Experience maintaining, calibrating, and troubleshooting laboratory equipment.</li><li>Bachelors degree in a scientific discipline, preferably chemistry, biochemistry, biology, molecular biology, or a related field.</li><li>Experience following SOPs and GDP documentation practices.</li><li>Hands-on analytical laboratory experience in a regulated environment.</li><li>Strong computer skills, including proficiency with Microsoft Office and laboratory software.</li><li>Strong analytical and problem-solving abilities</li></ul>Work EnvironmentThis role is based in a regulated laboratory environment that emphasizes compliance with cGMP, GLP, GDP, and established quality systems. You work with a variety of analytical instruments and technologies, including HPLC, ICP-MS, UV-Vis spectroscopy, flow cytometry, NMR, dissolution testing equipment, and general organic chemistry tools, as well as LIMS and other analytical software. The laboratory follows strict contamination-control and safety procedures, and appropriate PPE is required. The position offers a comprehensive benefits package, including paid time off, paid holidays, medical, dental, and vision coverage, a 401(k) retirement plan, a health savings account, life insurance, short-term and long-term disability, an employee assistance program, and transportation benefits, supporting a stable and well-rounded work experience.Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Pay and BenefitsThe pay range for this position is $26.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Eugene, OR.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Eugene,OR.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Job Title: QC Stability ManagerJob DescriptionThe QC Stability Manager is responsible for leading and maintaining stability programs that support clinical and commercial cell and gene therapy products. This role serves as the stability subject matter expert and primary point of contact for all stability-related activities across internal teams, contract manufacturing organizations, and contract testing laboratories. The position plays a critical role in ensuring robust stability strategies, compliant execution of studies, and high-quality data to support shelf-life, storage conditions, and regulatory submissions for advanced therapies.Responsibilities<ul><li>Manage and oversee stability programs and studies that support clinical and commercial cell therapy products, ensuring alignment with quality and regulatory expectations.</li><li>Author, review, and approve stability protocols, study plans, reports, and all related documentation to ensure scientific soundness and regulatory compliance.</li><li>Coordinate the stability program end-to-end, including long-term, accelerated, in-use, freeze-thaw, transport, and comparability studies, driving timely execution and adherence to approved protocols.</li><li>Review, analyze, and trend stability data to support shelf-life assignments, expiry dating, storage conditions, and product quality decisions.</li><li>Oversee stability activities conducted by contract manufacturing organizations, external suppliers, and contract testing laboratories, ensuring compliance with quality standards and regulatory requirements.</li><li>Monitor overall stability program performance, maintain study tracking systems, and proactively communicate study status, data trends, and risks to key stakeholders.</li><li>Support batch disposition activities by reviewing quality control data and providing stability-related input to product release decisions.</li><li>Lead or support investigations related to stability failures, out-of-specification (OOS) and out-of-trend (OOT) results, laboratory deviations, and product quality issues, ensuring thorough root cause analysis and effective corrective actions.</li><li>Author and review stability-related content for regulatory documentation and support regulatory inspections, audits, and submissions.</li><li>Collaborate closely with internal cross-functional groups, including CMC and Quality, to align stability strategies with overall product development and commercialization plans.</li><li>Engage with external partners, including CDMOs/CMOs and contract laboratories, to coordinate stability activities, resolve issues, and maintain strong communication channels.</li></ul>Essential Skills<ul><li>Bachelors degree with 7+ years or Masters degree with 5+ years of experience in biotechnology, pharmaceutical, biologics, cell and gene therapy, or related industries.</li><li>At least 5+ years of experience managing or supporting GMP stability programs for clinical and/or commercial products.</li><li>Direct experience performing or overseeing release assays specific to cell therapies and supporting product quality assessments within a GMP environment.</li><li>Demonstrated experience managing stability activities performed by CMOs, contract testing laboratories, and external suppliers.</li><li>Hands-on experience with stability study design, execution, data analysis, trending, and reporting.</li><li>Strong knowledge of GMP regulations, ICH stability guidelines, and applicable global regulatory requirements related to stability.</li><li>Proficiency in working with stability programs and stability assays, including handling OOS and OOT results.</li><li>Ability to lead and contribute to investigations related to stability failures, OOS, OOT, and laboratory deviations.</li><li>Strong analytical skills and attention to detail when reviewing and interpreting stability data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting regulatory submissions such as IND, CTA, BLA, NDA, MAA, or equivalent.</li><li>Experience with electronic Quality Management Systems (eQMS) and electronic laboratory notebooks.</li><li>Experience supporting batch disposition and QC activities for cell and gene therapy products.</li><li>Background in startup or fast-paced biotechnology environments, with the ability to adapt to evolving priorities.</li><li>Experience applying statistical tools to evaluate stability trends and support shelf-life determinations.</li><li>Strong communication skills, with the ability to clearly present data trends and study outcomes to internal and external stakeholders.</li><li>Ability to collaborate effectively with CMC, Quality, and external partners to align stability strategies with product development goals.</li><li>Understanding of the role of Quality and Compliance in successful regulatory filings for advanced therapies.</li></ul>Work EnvironmentThis is a first-shift hybrid role with an expectation of one day onsite per week, providing a balance of remote and on-site work. A laptop will be provided to support daily responsibilities and collaboration with internal teams and external partners. The organization is a late-stage clinical biotechnology company focused on developing and launching curative targeted cell therapies for autoimmune diseases, where Quality and Compliance play a critical role in achieving successful regulatory filings. The environment is fast-paced and growth-oriented, offering the opportunity to contribute meaningfully to the advancement and commercialization of innovative therapies. While on contract, you will receive accrued paid time off, six paid holidays, health, dental, and vision benefits, as well as access to a 401(k) plan.Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $57.69 - $62.50/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a hybrid position in Philadelphia,PA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Stability Manager

Job Title: QC Supervisor (3rd Shift)Job DescriptionThe QC Supervisor oversees all quality control laboratory activities on 3rd shift (12:00 a.m. 8:00 a.m., Monday through Friday). This role manages laboratory operations, ensures accurate and compliant analytical testing, and provides technical support for routine processes and new products within a regulated GMP environment.Responsibilities<ul><li>Accept full responsibility for managing the quality control laboratory during the assigned shift.</li><li>Provide analytical support for routine processes and new product introductions in accordance with GMP requirements.</li><li>Manage the maintenance and calibration of laboratory equipment to ensure accurate and reliable performance.</li><li>Oversee documentation of raw materials, intermediates, in-process controls (IPCs), stability and cleaning samples, ensuring accuracy and compliance.</li><li>Review existing standard operating procedures (SOPs) and SOPQs and write new procedures as needed for new equipment, technologies, or processes.</li><li>Participate in the description and optimization of technical procedures and the review of analytical methods.</li><li>Initiate and manage change controls related to documentation, systems, and quality control laboratory reports.</li><li>Support the introduction and implementation of new work procedures in the laboratory.</li><li>Approve or reject raw materials, intermediates, in-process controls, stability samples, and cleaning samples based on analytical results and established criteria.</li><li>Ensure timely and accurate equipment maintenance and calibration activities are documented and completed.</li><li>Prepare and review analytical records in accordance with current SOPs and SOPQs for approval or rejection decisions.</li><li>Maintain order, cleanliness, and organization within the laboratory to support efficient and safe operations.</li><li>Oversee data entry and calculations in laboratory systems, ensuring accuracy and completeness, and generate analytical records and bulletins as required.</li><li>Control and manage the sample library, including proper storage, tracking, and retrieval of samples.</li><li>Write and investigate deviations, out-of-specification (OOS), out-of-trend (OOT), out-of-expectation (OOE) results, and other laboratory events, ensuring thorough documentation and follow-up.</li><li>Promote and ensure compliance with Health, Safety and Environment procedures, quality standards, GMP systems, and Data Integrity principles after receiving appropriate training.</li><li>Support and drive continuous improvement by identifying, defining, and implementing initiatives that increase efficiency and optimize the use of available resources.</li><li>Collaborate with laboratory leadership and other stakeholders to ensure alignment with organizational quality and operational goals.</li><li>Provide guidance and day-to-day leadership to a small team of analysts on 3rd shift, fostering a culture of quality, safety, and continuous improvement.</li></ul>Essential Skills<ul><li>Degree in Sciences, preferably in Chemistry or Pharmacy.</li><li>Minimum of 3+ years of chemistry laboratory experience within a GMP environment (such as food, pharmaceutical, medical device, or chemical industries).</li><li>Strong knowledge of analytical chemistry principles and laboratory practices.</li><li>Hands-on experience with wet chemistry techniques.</li><li>Practical experience with high-performance liquid chromatography (HPLC).</li><li>Experience with gas chromatography (GC) and related chromatographic techniques.</li><li>Understanding of GMP regulations and quality systems in a regulated environment.</li><li>Experience working with raw materials, intermediates, in-process controls (IPCs), stability samples, and cleaning samples, including approvals and rejections.</li><li>Familiarity with data review and data integrity requirements, including ALCOA and ALCOA+ principles and audit trail review.</li><li>Training in Health, Safety and Environment practices applicable to laboratory operations.</li><li>Training on analytical techniques such as HPLC, HRGC, GC, FTIR, and related methods.</li><li>Proficiency with Microsoft Office applications, particularly Excel and Word.</li><li>Ability to write, review, and implement SOPs and other controlled documentation.</li><li>Experience investigating deviations, OOS, OOT, OOE, and laboratory events and documenting findings clearly.</li><li>Strong attention to detail, organizational skills, and ability to manage multiple tasks in a fast-paced environment.</li><li>Ability to work independently on a night shift while providing guidance to other analysts.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a pharmaceutical or medical device QC laboratory environment.</li><li>Familiarity with chromatography data systems such as Empower and Chromeleon.</li><li>Experience working with Agilent instrumentation and associated software.</li><li>Knowledge of mass spectrometry and its application in analytical testing.</li><li>Understanding of data integrity tools and practices, including audit trail review and compliance.</li><li>Experience in a contract development and manufacturing (CDMO) or similar project-based environment.</li><li>Demonstrated ability to support new product introduction and method transfer activities.</li><li>Strong communication skills to collaborate effectively with laboratory leadership and cross-functional teams.</li><li>Proven ability to promote continuous improvement initiatives in laboratory operations.</li></ul>Work EnvironmentThis role is based in a quality control laboratory operating on 3rd shift, with core hours from 12:00 a.m. to 8:00 a.m., Monday through Friday. The QC Supervisor initially trains on 1st shift for approximately one month to become familiar with laboratory procedures, systems, and equipment before transitioning to 3rd shift. On 3rd shift, the supervisor works with a small team, typically two analysts, and serves as the on-site laboratory resource during those hours. The environment involves routine use of analytical technologies such as HPLC, gas chromatography, mass spectrometry, FTIR, and chromatography data systems like Empower, Chromeleon, and Agilent platforms. Work is conducted under strict GMP, quality, and data integrity standards, with a strong emphasis on Health, Safety and Environment practices. The laboratory setting is structured, regulated, and process-driven, offering opportunities for professional growth and advancement as additional customer projects and workstreams are integrated into the organization.Job Type &amp; LocationThis is a Contract to Hire position based out of Morton Grove, IL.Pay and BenefitsThe pay range for this position is $34.00 - $40.87/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Morton Grove, IL.Application DeadlineThis position is anticipated to close on Nov 4, 2026.Workplace TypeThis is a fully onsite position in Morton Grove,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Supervisor

Job Title: QC Supervisor Environmental Monitoring &amp; MetrologyJob DescriptionThe QC Supervisor Environmental Monitoring &amp; Metrology leads and supports the Environmental Monitoring, Cleaning Validation, and Metrology teams within a modern, growing quality control laboratory. This role oversees critical activities such as environmental monitoring, cleaning verification and validation, and equipment calibration, ensuring compliance with cGMP requirements and alignment with production priorities. The supervisor collaborates closely with cross-functional teams, drives investigations and continuous improvement, and mentors a team of chemists in a fast-paced, dynamic environment.Responsibilities<ul><li>Lead and support the Environmental Monitoring, Cleaning Validation, and Metrology teams to ensure all activities meet quality and regulatory expectations.</li><li>Prioritize daily work based on Production needs, especially when manufacturing is waiting on cleaning verification or environmental testing results.</li><li>Oversee environmental monitoring activities, including sampling, testing, data trending, and investigations related to environmental monitoring failures.</li><li>Manage cleaning verification and cleaning validation to ensure manufacturing equipment and suites consistently meet established cleaning requirements.</li><li>Coordinate cleaning activities with Production, Formulations, QC, and QA, ensuring timely resolution of issues and alignment with manufacturing schedules.</li><li>Take a big-picture view when issues arise to confirm that cleaning requirements and procedures are followed and effectively implemented.</li><li>Lead or support investigations related to environmental monitoring, cleaning, equipment, or calibration issues, and drive corrective and preventive actions.</li><li>Oversee equipment calibration, preventive maintenance, and qualification activities to maintain compliance and reliable instrument performance.</li><li>Help troubleshoot laboratory equipment and support teams in resolving technical issues with instruments such as HPLC, GC, and dissolution systems.</li><li>Review and approve SOPs, protocols, reports, and other documentation related to Environmental Monitoring, Cleaning Validation, and Metrology.</li><li>Participate in client and regulatory audits, providing subject matter expertise for environmental monitoring, cleaning validation, and metrology processes.</li><li>Mentor, train, and develop team members, supporting their technical growth and helping them adapt to changing priorities and production demands.</li><li>Promote a collaborative team environment, encouraging open communication and continuous learning across QC and related departments.</li><li>Ensure all work complies with cGMP standards, internal procedures, and applicable regulatory requirements.</li><li>Effectively manage time, resources, and schedules to balance multiple projects and shifting priorities.</li></ul>Essential Skills<ul><li>B.S. degree in chemistry, biochemistry, biology, or a related life science field.</li><li>At least 3 years of cGMP experience in a laboratory or pharmaceutical/biotech manufacturing environment.</li><li>Experience in environmental monitoring and/or cleaning validation in a regulated setting (strongly preferred).</li><li>Leadership experience supervising employees or leading teams, projects, or process improvement initiatives.</li><li>Hands-on experience with analytical chemistry techniques such as HPLC, GC, titration, and wet chemistry.</li><li>Strong background in quality control and QC testing within a cGMP framework.</li><li>Experience in metrology, equipment qualification, or calibration (preferred).</li><li>Familiarity with laboratory equipment operation and basic troubleshooting, including systems such as HPLC, GC, and dissolution instruments.</li><li>Experience with systems such as Empower, LIMS, or MasterControl (helpful).</li><li>Strong organizational and time-management skills with the ability to handle changing priorities.</li><li>Proactive, self-motivated approach with a strong sense of urgency and ownership.</li><li>Ability to see the bigger picture, ask thoughtful questions, and drive issues to resolution.</li><li>Strong communication skills with the ability to work effectively with Production, QA, QC, and other cross-functional teams.</li><li>Approachable and patient leadership style with the ability to support, coach, and motivate team members.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience leading cleaning validation projects and cleaning verification activities in a cGMP environment.</li><li>background in analytical development or method development is beneficial.</li><li>Demonstrated ability to lead investigations and implement corrective and preventive actions.</li><li>Experience working in a multi-team QC structure (e.g., Raw Materials, Finished Products, Analytical Development, Environmental Monitoring).</li><li>Ability to lead or support process improvements that enhance efficiency, data integrity, and compliance.</li><li>Comfort working in a fast-paced environment where priorities can shift based on production needs.</li></ul>Work EnvironmentThis position is based in a quality control laboratory environment with dedicated Environmental Monitoring and Metrology teams consisting of approximately six chemists. The role backfills a team member who has been promoted to a manager-level position, reflecting strong internal growth opportunities. On the chemistry side, the QC lab is organized into four teamsRaw Materials, Finished Products, Analytical Development, and Environmental Monitoring/QC Specialistseach typically led by a supervisor overseeing around six chemists. The laboratory has expanded over the last two years and has been recently remodeled, offering a modern, clean, and collaborative workspace. Chemists work at shared workstations rather than individual desks, fostering a team-oriented environment, while scientist-level staff have dedicated desks. All chemists are equipped with laptops and work with a variety of analytical instruments, including HPLC, GC, dissolution systems, and other QC equipment. The work is varied, providing exposure to multiple techniques and instruments and encouraging ongoing learning and development. The role is full-time, with a standard laboratory schedule aligned to production and QC needs. The organization offers a competitive benefits package that includes a sign-on bonus, paid holidays (including New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving Day and the day after, Christmas Eve, and Christmas Day), and a robust paid time off program. Full-time employees accrue up to 17 days (136 hours) of PTO in their first year and 22 days (176 hours) per year after the first 12 months, with rollover allowed subject to a maximum accrual based on years of service. Accrued PTO can be used immediately, with supervisor approval, for both contract and permanent employees. The culture emphasizes teamwork, professional growth, and continuous learning in a modern laboratory setting.Job Type &amp; LocationThis is a Permanent position based out of Verona, WI.Pay and BenefitsThe pay range for this position is $65000.00 - $85000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Competitive Benefits Include:

$0 monthly premium for medical insurance
$0 monthly premium option for dental insurance
Friendly work environment
Medical, dental, vision, life, AD&amp;D, and disability insurance
Pre-tax 401(k) and after-tax Roth 401(k) contribution options with company matching up to 5%
Generous paid time off, accruing up to 17 days of PTO within your first year
Tuition reimbursement program
Sign-on bonusJob Type &amp; LocationThis is a Permanent position based out of Verona, WI.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Verona,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Supervisor- Environmental Monitoring/Metrology

Job Title: QC Supervisor Raw MaterialsJob DescriptionThe QC Supervisor Raw Materials leads and develops the Raw Materials Quality Control team, ensuring timely, accurate testing and release of pharmaceutical, nutraceutical, and industrial raw materials to support production and formulation timelines. This role manages a fast-paced workload with shifting priorities, provides technical and troubleshooting support in a cGMP laboratory environment, and collaborates closely with internal teams and external clients to maintain high quality and regulatory standards.Responsibilities<ul><li>Lead, mentor, train, and supervise the Raw Materials QC team while providing support to the Finished Product QC team as needed.</li><li>Prioritize and coordinate raw material testing and release activities to ensure materials are available to meet Production and Formulations schedules.</li><li>Manage a fast-paced workload with multiple priorities, frequent interruptions, and evolving testing needs, while maintaining high quality standards.</li><li>Work closely with Production and Formulations teams to communicate testing status, priorities, issues, and raw material release timelines.</li><li>Oversee testing and analysis of pharmaceutical, nutraceutical, and industrial raw materials according to USP, EP, internal specifications, analytical methods, compendial monographs, and client requirements.</li><li>Maintain strong working knowledge of USP and EP raw material requirements and stay current with applicable regulatory and compendial standards, including ICH, FDA, FCC, EU, and JP requirements.</li><li>Lead raw material investigations, including deviations, quality investigations, and Out-of-Specification (OOS) results, ensuring thorough root cause analysis and appropriate corrective actions.</li><li>Partner closely with Quality and external clients during investigations, providing clear updates and effectively communicating technical findings.</li><li>Review and approve SOPs, analytical methods, material specifications, deviations, OOS investigations, protocols, and summary reports for accuracy and compliance.</li><li>Oversee and troubleshoot laboratory testing using HPLC, GC, UV, titration, and other wet chemistry techniques.</li><li>Provide technical guidance and troubleshooting support to Chemists and Scientists on analytical methods, testing issues, and laboratory equipment.</li><li>Support method validations, method transfers, method verifications, and routine stability studies for raw materials.</li><li>Perform and oversee analytical data review to ensure that testing and documentation meet established procedures, cGMP expectations, and quality requirements.</li><li>Coordinate activities with internal teams, clients, contract laboratories, and vendors related to testing, documentation, shipping, purchasing, quoting, and billing.</li><li>Generate and review QC metrics and provide regular workload and testing updates to leadership.</li><li>Promote strong laboratory practices and ensure compliance with applicable cGMP, safety, and quality procedures at all times.</li><li>Conduct annual performance reviews and hold regular meetings with direct reports to provide feedback, coaching, and development opportunities.</li></ul>Essential Skills<ul><li>B.S. degree in chemistry, biochemistry, biology, or a related life science field.</li><li>At least 3 years of cGMP experience in a laboratory or quality control environment.</li><li>Strong knowledge of USP, with experience in USP and EP raw material testing highly preferred.</li><li>Hands-on experience with HPLC and GC in an analytical chemistry or quality control setting.</li><li>Proficiency in wet chemistry techniques, including titration and related methods.</li><li>Demonstrated leadership experience, either through direct supervision of staff or strong project/team leadership.</li><li>Quality control and QC testing experience with raw materials in a regulated environment.</li><li>Ability to prioritize effectively, take ownership of responsibilities, and operate with a sense of urgency.</li><li>Experience working within systems such as Empower, LIMS, and/or MasterControl.</li><li>Strong verbal and written communication skills, with the ability to work collaboratively with clients and cross-functional teams.</li><li>Ability to troubleshoot analytical methods and laboratory equipment and provide technical guidance to team members.</li><li>Solid understanding of cGMP, safety, and quality procedures in a laboratory setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience leading or contributing to method validations, method transfers, method verifications, and stability studies.</li><li>Familiarity with regulatory and compendial standards such as ICH, FDA, FCC, EU, and JP requirements.</li><li>Experience coordinating with contract laboratories and vendors for testing, documentation, and logistics.</li><li>Strong data review skills with attention to detail and adherence to established procedures and quality requirements.</li><li>Ability to generate, interpret, and present QC metrics and workload reports to leadership.</li><li>Proven ability to manage multiple priorities and adapt to frequent interruptions in a dynamic laboratory environment.</li><li>Comfort working in smaller, collaborative teams with a focus on continuous learning and exposure to varied instrumentation.</li><li>Demonstrated ability to build positive working relationships across Production, Formulations, Quality, and external clients.</li></ul>Work EnvironmentThis role operates within a modern, expanding Quality Control laboratory focused on raw material testing. The Raw Materials team consists of approximately six chemists, and the position backfills a team member who has been promoted into a managerial role, offering clear growth potential. On the chemistry side, there are four primary teamsRaw Materials, Finished Products, Analytical Development, and Environmental Monitoring/QC Specialistswith each supervisor typically overseeing around six chemists. The lab has been remodeled to provide a contemporary, collaborative environment, with shared workspaces for chemists below the scientist level and individual desks for scientist-level staff. All chemists have access to laptops and work in shared spaces designed to foster teamwork and communication. The laboratory uses a variety of analytical instruments and systems, including HPLC, GC, UV, wet chemistry equipment, Empower, LIMS, and MasterControl, providing exposure to diverse techniques and ongoing learning opportunities. The workload is fast-paced with multiple priorities and frequent interactions across internal teams and external clients. The organization offers a competitive benefits package that includes a sign-on bonus, eight paid holidays, and a generous paid time off program with accrual that increases after the first year and allows rollover. Employees can use accrued PTO immediately, with supervisor approval, and this policy applies equally to contract and permanent employees. The culture emphasizes teamwork, professional development, and varied, engaging work in a modern QC lab setting.Job Type &amp; LocationThis is a Permanent position based out of Verona, WI.Pay and BenefitsThe pay range for this position is $65000.00 - $85000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Competitive Benefits Include:

$0 monthly premium for medical insurance
$0 monthly premium option for dental insurance
Friendly work environment
Medical, dental, vision, life, AD&amp;D, and disability insurance
Pre-tax 401(k) and after-tax Roth 401(k) contribution options with company matching up to 5%
Generous paid time off, accruing up to 17 days of PTO within your first year
Tuition reimbursement program
Sign-on bonusJob Type &amp; LocationThis is a Permanent position based out of Verona, WI.Application DeadlineThis position is anticipated to close on Nov 16, 2026.Workplace TypeThis is a fully onsite position in Verona,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Supervisor- Raw Materials

Job Title: QC TechnicianJob DescriptionThe QC Technician supports food safety and quality programs by performing laboratory testing, monitoring production lines, and ensuring all products meet established specifications and regulatory requirements. This role focuses on accurate testing, proper documentation, and active participation in food safety and quality systems within a busy, high-volume manufacturing environment.Responsibilities<ul><li>Ensure all parameters of food safety and product quality are consistently adhered to and maintained in the laboratory and designated production areas.</li><li>Calibrate laboratory and line equipment to ensure accurate and reliable test results.</li><li>Collect in-process and finished product samples and perform standardized qualitative and quantitative testing to verify conformance to specifications.</li><li>Perform and record product evaluation tests in accordance with HACCP plans, Standard Operating Procedures (SOPs), and other food safety and quality programs.</li><li>Accurately document and record all required information in the computer system following SOPs and established data entry protocols.</li><li>Conduct ATP testing as part of the allergen control program to verify sanitation effectiveness.</li><li>Perform microbiological testing as required to support food safety verification.</li><li>Maintain a retain sample library, ensuring proper storage, labeling, and traceability of product samples.</li><li>Recognize quality deficiencies and initiate appropriate follow-up actions to address nonconformances.</li><li>Identify and isolate product that does not meet quality or safety standards and ensure it is properly held and controlled.</li><li>Perform QC tasks including product sampling, line monitoring, auditing, laboratory testing, and equipment calibration to ensure compliance with specifications.</li><li>Hold products that do not meet quality standards and determine appropriate dispositions in line with company policies and procedures.</li><li>Interpret and understand all information contained within product specification sheets.</li><li>Maintain detailed knowledge of the quality characteristics and requirements for each product packaged.</li><li>Conduct laboratory testing procedures such as brix, refractive index, pH, density, sensory evaluation, weights, moisture analysis, and related tests.</li><li>Operate and maintain laboratory instruments including pH meters, viscosity meters, and gas chromatographymass spectrometry (GCMS) equipment.</li><li>Understand and comply with Good Manufacturing Practices (GMPs), food safety regulations, and all applicable SOPs.</li><li>Collaborate with production and quality teams to support continuous improvement of food safety and quality processes.</li><li>Support production operations across all required days to ensure the laboratory is staffed in alignment with production schedules.</li></ul>Essential Skills<ul><li>Experience in quality control within a food manufacturing or laboratory environment.</li><li>Hands-on proficiency using pH meters, viscosity meters, UV-visual measurement equipment, and related laboratory instruments.</li><li>Ability to perform food-related laboratory testing including brix, refractive index, pH, density, sensory evaluation, weights, and moisture analysis.</li><li>Strong understanding of food science or chemistry principles applied to quality control and product testing.</li><li>Working knowledge of gas chromatography techniques and equipment (GCMS).</li><li>Familiarity with HACCP plans, GMPs, SOPs, and food safety and quality programs.</li><li>Ability to accurately document test results and maintain organized records in computer systems.</li><li>Capability to recognize quality deficiencies and take appropriate corrective actions.</li><li>Ability to wear a half-face respirator when working with specific chemicals in production.</li><li>Willingness and ability to work evenings, weekdays, and some weekends in support of production schedules.</li><li>Demonstrated interest in working in and remaining within the food industry.</li></ul>Additional Skills &amp; Qualifications<ul><li>AA, BA, or BS degree in Food Science, Chemistry, or a related scientific field, OR at least 1 year of food quality control experience with specific lab testing responsibilities.</li><li>Experience conducting laboratory procedures such as brix, refractive index, pH, density, sensory evaluation, weights, and moisture testing in a food production setting.</li><li>Background in wholesale flavor, color, or ingredient manufacturing is beneficial.</li><li>Strong attention to detail and commitment to maintaining high quality and food safety standards.</li><li>Ability to work effectively in a fast-paced, high-volume production environment.</li><li>Comfort with rotating schedules and adapting to changing production needs.</li><li>Reliability and flexibility to support a 6-day workweek when required.</li><li>Interest in long-term career growth in food science, quality assurance, or laboratory roles.</li></ul>Work EnvironmentThis role is based in a laboratory setting within a busy food manufacturing facility, focusing on testing food products for pH, viscosity, and other quality parameters. The environment supports high production volumes, with production operating 7 days a week and the lab staffed to align with these operations. The QC Technician works primarily on second shift, typically from 4:00 p.m. to 12:30 a.m., Monday through Friday, with the expectation of working a 6-day week that includes one weekend day on a rotating basis. Weekend shifts on Saturday or Sunday may have different hours than the regular weekday shift, and scheduling aims to avoid back-to-back weekends when possible, though this may occur to cover sick time or vacations. The facility operates two production shifts Monday through Saturday and one shift on Sunday morning, requiring flexible lab coverage. Work involves routine use of laboratory equipment such as pH meters, viscosity meters, UV-visual measurement devices, and GCMS, as well as occasional use of a half-face respirator when handling specific chemicals in production. The culture emphasizes strong food safety and quality standards, continuous production support, and offers sick time for consultants and fully paid benefits upon conversion to permanent employment. Attire is typical for a food manufacturing and laboratory environment, including appropriate protective equipment and compliance with safety and hygiene requirements.Job Type &amp; LocationThis is a Contract to Hire position based out of Commerce, CA.Pay and BenefitsThe pay range for this position is $20.00 - $20.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Commerce, CA.Application DeadlineThis position is anticipated to close on Nov 11, 2026.Workplace TypeThis is a fully onsite position in Commerce,CA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Tech

Job Title: QC Technician (1st Shift)Job DescriptionThe QC Technician is responsible for all phases of incoming sampling and inspection of raw materials, components, primary and secondary labeling, and other manufacturing operating supplies in accordance with applicable specifications and procedures. This role ensures that all materials meet current Good Manufacturing Practices (cGMP) and other regulatory requirements, and that they are accurately evaluated and properly dispositioned following established Standard Operating Procedures (SOPs). The QC Technician works with minimal supervision, maintains precise documentation, and supports overall quality control and quality assurance activities.Responsibilities<ul><li>Perform incoming sampling and inspection of all raw materials, components, primary and secondary labeling, and other manufacturing operating supplies in accordance with applicable specifications and procedures.</li><li>Ensure all materials pending disposition are held in the appropriate, designated locations until final disposition is assigned.</li><li>Sample materials according to the applicable SOPs and material specifications, following defined sampling plans and techniques.</li><li>Sample and inspect materials using the appropriate tools, instruments, and personal protective equipment (PPE) to ensure safe and accurate evaluations.</li><li>Verify that materials meet applicable requirements by using the inspection methods described in SOPs and material specifications.</li><li>Follow strict cGMP guidelines to ensure that materials maintain the safety, identity, strength, quality, and purity that they are intended or represented to possess.</li><li>Maintain accurate, complete, and legible records for all inspected materials, ensuring traceability and compliance with documentation standards.</li><li>Determine the disposition of materials (such as accept, reject, or other defined status) based on inspection results, specifications, and applicable procedures.</li><li>Complete all required documentation when materials are dispositioned and route the records to the appropriate departments in a timely manner.</li><li>Properly identify and label materials with the correct disposition status and all required information, ensuring clear communication throughout the facility.</li><li>Assist in the training of incoming inspectors by demonstrating proper sampling, inspection, documentation, and cGMP practices.</li><li>Support Quality Release management when requested by providing inspection results, documentation, and other relevant information.</li><li>Assist QC Management with various tasks and responsibilities as needed to support departmental objectives and continuous improvement initiatives.</li><li>Collaborate effectively with colleagues across QC, QA, and manufacturing to resolve issues related to incoming materials and quality standards.</li><li>Work with minimal supervision while maintaining high standards of accuracy, compliance, and productivity.</li></ul>Essential Skills<ul><li>High School Diploma required.</li><li>Bachelors degree preferred, ideally in a scientific discipline.</li><li>12 years of related experience in quality control, laboratory operations, or a similar field preferred.</li><li>Experience with quality control of raw materials, including sampling and inspection activities.</li><li>Working knowledge of cGMP (current Good Manufacturing Practices) and their application in a laboratory or manufacturing environment.</li><li>Experience with quality assurance principles and document control practices.</li><li>Ability to perform inspections and sampling using appropriate tools, instruments, and PPE.</li><li>Strong written communication skills for accurate and compliant documentation.</li><li>Strong verbal communication skills to collaborate effectively with colleagues and support training activities.</li><li>Good mathematical skills to perform calculations related to sampling, measurements, and data recording.</li><li>Ability to work well with others and contribute to a collaborative team environment.</li><li>Ability to work with minimal supervision while maintaining high standards of accuracy and compliance.</li><li>Attention to detail and strong organizational skills for managing multiple materials and documentation requirements.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in biology or a related scientific discipline is beneficial.</li><li>Experience working in a QC laboratory environment and on a manufacturing floor.</li><li>Familiarity with inspection methods and tools used for evaluating raw materials and components.</li><li>Experience with quality control documentation, including inspection records, labels, and disposition forms.</li><li>Exposure to quality assurance processes, including quality release activities.</li><li>Ability to assist in training new or incoming inspectors on sampling, inspection, and documentation procedures.</li><li>Demonstrated reliability and accountability in following SOPs and regulatory requirements.</li><li>Interest in long-term opportunities with potential to transition to a permanent role.</li></ul>Work EnvironmentThe QC Technician works across a QC laboratory, manufacturing floor, and QC office settings, performing sampling and inspection activities in a regulated environment. This is a 1st shift position, scheduled Monday through Friday from 8:00 a.m. to 4:30 p.m. The role involves regular use of inspection tools, laboratory equipment, and personal protective equipment (PPE) to ensure safe handling of materials and adherence to cGMP standards. The position requires careful movement and storage of materials awaiting disposition, consistent documentation practices, and collaboration with quality and manufacturing teams in a structured, process-driven environment. The facility operates under strict SOPs and regulatory guidelines, providing a professional setting focused on product quality and continuous improvement.Job Type &amp; LocationThis is a Contract to Hire position based out of Bradley, IL.Pay and BenefitsThe pay range for this position is $21.50 - $21.50/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Bradley, IL.Application DeadlineThis position is anticipated to close on Nov 6, 2026.Workplace TypeThis is a fully onsite position in Bradley,IL.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QC Technician

Job Title: Quality InspectorJob DescriptionThe Quality Inspector will perform a variety of parts and product inspections to meet company and customer requirements. The role involves inspecting incoming parts, documenting inspection results in written or photo format, gathering data, and creating reports for customers. Additionally, the inspector will communicate quality discrepancies to shop supervisors and maintain material certifications and inspection documentation.Responsibilities<ul><li>Inspect incoming sub out parts.</li><li>Document results of inspections (written/photo).</li><li>Gather data and create reports for customers.</li><li>Communicate quality discrepancies to shop supervisors.</li><li>Maintain material certifications and inspection documentation.</li><li>Maintain calibration control for all IMTE inventory.</li><li>Perform inspections to ISO standards.</li><li>Notify management of need for CWI.</li><li>Use basic measurement tools such as combination square, protractor, and caliper.</li><li>Assist with sub out process request purchase order, tag, and document count.</li><li>Label nonconforming parts.</li><li>Read blueprints to ensure fabricated product meets specifications.</li><li>Maintain calibration control for all inventory.</li><li>Follow all safety procedures.</li><li>Perform other responsibilities as assigned by supervisor.</li></ul>Essential Skills<ul><li>Quality control</li><li>Quality assurance</li><li>Quality inspection</li><li>Blueprint reading</li><li>Inspection</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in Quality Control Technology from an accredited college, or 3+ years proven inspection experience in lieu of a degree.</li><li>Minimum of 2+ years of experience as an inspector in a close tolerance, custom metal manufacturing business.</li><li>Experience in a metal forming, machining, and/or welding environment is preferred.</li><li>Demonstrated competency in blueprint reading and use of precision measurement equipment.</li><li>General machining and welding knowledge is a plus.</li><li>Knowledge of metals and raw materials, along with understanding of production processes, quality control, and costs of manufacturing is a plus.</li></ul>Work EnvironmentThe work environment involves working in a close tolerance, custom metal manufacturing business. The role requires familiarity with metal forming, machining, and/or welding processes, and adhering to all safety procedures.Job Type &amp; LocationThis is a Contract to Hire position based out of Green Bay, WI.Pay and BenefitsThe pay range for this position is $28.00 - $30.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Green Bay, WI.Application DeadlineThis position is anticipated to close on Nov 19, 2026.Workplace TypeThis is a fully onsite position in Green Bay,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

QUALITY INSPECTOR

Job Title: QMS SpecialistJob DescriptionThe QMS Specialist will support a sixmonth documentation and compliance project focused on updating existing Control Plans, PFMEAs, and process flow charts and transitioning them from Excel into the Nexus system. Many of these quality documents are approximately 25 years old and were not updated when applicable standards changed in 2019, so this role involves detailed review, technical analysis, and improvement rather than simple data entry. The specialist will collaborate closely with Production Engineers across multiple departments to ensure all documents are accurate, current, and aligned with relevant standards before they are entered into Nexus.Essential Skills<ul><li>Hands-on experience updating PFMEAs and Control Plans within a quality documentation context.</li><li>Practical knowledge of IATF requirements and their application in a quality management system.</li><li>Experience working with quality management systems (QMS) and document control processes.</li><li>Proficiency in Microsoft Excel, Word and Teams</li><li>Strong attention to detail and accuracy when reviewing and updating technical documentation.</li><li>Ability to interpret technical information and translate it into clear, compliant quality documents.</li></ul>Additional Skills &amp; Qualifications<ul><li>VDA experience is a plus, particularly in relation to automotive quality standards and documentation.</li><li>Familiarity with automotive Tier 1 supplier environments is beneficial.</li><li>Experience working with or transitioning documentation into electronic quality systems such as Nexus is an advantage.</li><li>Background in quality assurance, quality engineering, or related fields is preferred.</li><li>Understanding of process flow charting and risk analysis within manufacturing environments.</li></ul>Work EnvironmentThe QMS Specialist will work in a structured office and production-support environment, collaborating closely with Quality and Production Engineering teams. The role follows a standard schedule of 8:00 a.m. to 5:00 p.m., Monday through Friday. Work will involve extensive use of Microsoft Excel, Word, Teams, and the Nexus system to review, update, and manage quality documentation. The environment supports focused, detail-oriented work and regular interaction with cross-functional stakeholders in an automotive Tier 1 supplier setting.Job Type &amp; LocationThis is a Contract position based out of Battle Creek, MI.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract position based out of Battle Creek, MI.Application DeadlineThis position is anticipated to close on Nov 13, 2026.Workplace TypeThis is a fully onsite position in Battle Creek,MI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Qms Specialist

Job Title: Quality Assurance Analyst (Float Role)Job DescriptionThis Quality Assurance Analyst float role ensures that products consistently meet the highest standards of quality and safety in alignment with industry regulations and internal policies. The analyst supports multiple areas as needed, performing audits, testing, and documentation to maintain compliance with GMP, SQF, HACCP, FDA, and state regulations. The role works closely with operations, sanitation, and maintenance teams to uphold food safety protocols and drive continuous improvement across the facility.Responsibilities<ul><li>Ensure product quality and safety meet established standards, regulatory requirements, and internal policies across assigned areas.</li><li>Conduct routine and targeted quality audits, including case audits, self-inspections, and mock recalls, to verify compliance with GMP, SQF, HACCP, FDA, and state regulations.</li><li>Verify Certificates of Analysis (COAs) for raw materials and finished products to confirm they meet specified quality and safety criteria.</li><li>Perform microbiological testing and other laboratory analyses to monitor product and environmental quality.</li><li>Monitor and verify critical control points (CCPs) and other key parameters within HACCP and food safety plans.</li><li>Review batch records for accuracy, completeness, and compliance with GMP and FDA requirements.</li><li>Maintain accurate and detailed quality documentation, including test results, audit findings, and corrective actions.</li><li>Identify nonconformances and quality issues, perform root cause analysis, and support implementation of effective corrective and preventive actions.</li><li>Collaborate with operations, sanitation, and maintenance teams to reinforce food safety and quality standards and drive continuous improvement initiatives.</li><li>Support environmental monitoring programs to ensure the facility maintains appropriate hygiene and sanitation conditions.</li><li>Assist in preparation for and participation in regulatory, customer, and third-party audits.</li><li>Promote and uphold a culture of excellence, food safety, and regulatory compliance throughout the facility.</li><li>Provide flexible coverage as a float quality analyst, supporting different shifts or areas as needed.</li><li>Be available for occasional overtime and weekend work to support audits, food safety incidents, or other urgent quality needs.</li></ul>Essential Skills<ul><li>15 years of experience in a quality-related role with a degree in the sciences, or 5+ years of quality experience within a GMP/FDA-regulated facility.</li><li>Practical experience in quality assurance and quality control within a regulated environment.</li><li>Working knowledge of GMP (Good Manufacturing Practices) and FDA regulations.</li><li>Hands-on experience with HACCP and food safety programs, including monitoring critical control points.</li><li>Experience performing inspections, quality analysis, and quality documentation.</li><li>Ability to conduct batch record review for compliance and completeness.</li><li>Experience with environmental monitoring and microbiological testing in a lab or production environment.</li><li>Strong understanding of food safety principles and regulatory requirements.</li><li>Proficiency in root cause analysis and problem-solving in response to quality issues.</li><li>Ability to interpret and verify Certificates of Analysis (COAs).</li><li>Solid biology or related scientific background applicable to food safety and quality.</li><li>Strong attention to detail and accuracy in documentation and recordkeeping.</li><li>Ability to work the 8:00 p.m.4:30 a.m. shift Wednesday through Saturday, with flexibility for occasional weekend or overtime coverage.</li></ul>Additional Skills &amp; Qualifications<ul><li>Degree in a scientific discipline such as biology, food science, or a related field.</li><li>Experience working within SQF-certified or similarly certified food safety and quality systems.</li><li>Familiarity with mock recalls, self-inspections, and internal audit programs.</li><li>Experience collaborating with cross-functional teams such as operations, sanitation, and maintenance.</li><li>Strong communication skills to clearly document findings and convey quality expectations.</li><li>Ability to adapt as a float resource, supporting multiple areas or processes as needed.</li><li>Demonstrated commitment to continuous improvement and maintaining a culture of excellence in quality and food safety.</li></ul>Work EnvironmentThis role follows a regular schedule of Wednesday through Saturday, 8:00 p.m. to 4:30 a.m., with typical hours centered around the evening and overnight shift. The position is based in a GMP- and FDA-regulated facility that operates under strict food safety and quality standards, including SQF, HACCP, and environmental monitoring programs. The work environment includes both laboratory and production floor settings, requiring regular interaction with operations, sanitation, and maintenance teams. There may be occasional overtime and weekend work, particularly during audits or food safety emergencies, and candidates should be willing to provide additional coverage when necessary.Job Type &amp; LocationThis is a Permanent position based out of Oak Creek, WI.Pay and BenefitsThe pay range for this position is $68000.00 - $83000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.This is a direct placement opportunity. The benefits will be provided upon start of assignment or earlier if requested by candidate.Job Type &amp; LocationThis is a Permanent position based out of Oak Creek, WI.Application DeadlineThis position is anticipated to close on Nov 9, 2026.Workplace TypeThis is a fully onsite position in Oak Creek,WI.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Analyst Float Role

Job DescriptionJoin a dynamic QA Release Group and Process Team where you will play a critical role in ensuring the quality and compliance of our production processes with regulatory standards.Responsibilities<ul><li>Perform detailed review and approval of batch records and associated technical documentation for routine production, validation, and change control activities to ensure compliance with USDA, FDA, and EU regulations.</li><li>Provide real-time, on-the-floor quality support for batch reviews, process auditing, and quality guidance to production personnel and the Process Team.</li><li>Support the deviation management process by identifying non-conformances, determining root cause, and participating in investigation report writing.</li><li>Assist with internal and external inspection audits by helping with preparation and response, and support the Process Team by tracking and reporting on continuous improvement goals.</li><li>Execute usage decisions and release transactions in SAP to manage product movement and final disposition for product release.</li></ul>Essential Skills<ul><li>Quality assurance expertise.</li><li>Experience with batch record review and quality investigations.</li><li>Strong critical thinking skills.</li><li>Ability to take feedback well and be self-driven.</li><li>Demonstrated experience reviewing GMP-regulated documents such as batch records, SOPs, and quality investigations.</li><li>Proficiency with computer systems including Microsoft Suite, SAP, and Veeva.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's Degree in a scientific discipline</li><li>At least 1-2 years of experience in a GMP-regulated environment, such as pharmaceuticals or biologics.</li></ul>Work EnvironmentThe work schedule is Monday through Friday, 1st shift. The position offers flexibility around start and end times but requires working 8 hours per day, totaling 40 hours per week.Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Dodge, IA.Pay and BenefitsThe pay range for this position is $30.00 - $35.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 Medical, dental &amp; vision
 Critical Illness, Accident, and Hospital
 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
 Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 Short and long-term disability
 Health Spending Account (HSA)
 Transportation benefits
 Employee Assistance Program
 Time Off/Leave (PTO, Vacation or Sick Leave)Job Type &amp; LocationThis is a Contract to Hire position based out of Fort Dodge, IA.Application DeadlineThis position is anticipated to close on Nov 17, 2026.Workplace TypeThis is a fully onsite position in Fort Dodge,IA.About Actalent 

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.



The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.



If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email actalentaccommodation@actalentservices.com for other accommodation options.



San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.



Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.



Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.

Quality Associate

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