Description
					Support supply planning activities within SAP IBP, including demand and supply reviews, scenario analysis, exception management, and supply commitments.
Develop, maintain, and analyze supply plans supporting commercial, clinical, and non-GMP manufacturing operations.
Translate demand forecasts, inventory targets, manufacturing assumptions, and capacity constraints into actionable supply plans.
Partner with Operations and Manufacturing teams to ensure production schedules support on-time and in-full delivery objectives.
Create rough-cut capacity plans and provide scheduling inputs to support manufacturing and supply chain decision-making.
Identify and escalate supply risks, inventory constraints, capacity gaps, and data quality issues while providing recommendations for mitigation.
Participate in cross-functional planning meetings, including Tier meetings, S&amp;OE processes, and supply review discussions.
Maintain and validate SAP and SAP IBP master data, including materials, locations, planning parameters, lead times, and related attributes.
Support item lifecycle management and master data governance activities, including setup, modifications, approvals, and obsolescence processes.
Develop planning metrics, dashboards, and reporting tools to monitor supply plan performance, inventory levels, schedule adherence, and data accuracy.
Conduct ad hoc supply chain analyses related to product launches, budgeting, forecasting, inventory optimization, and risk assessments.
										Skills
					Sap, integrated business process, supply planning, production planning, master data, demand planning, capacity planning, supply chain, inventory management, manufacturing planning
										Top Skills Details
					Sap,integrated business process,supply planning,production planning,master data,demand planning,capacity planning,supply chain,inventory management,manufacturing planning
										Additional Skills &amp; Qualifications
					Bachelor's degree in Supply Chain, Engineering, Business, Operations Management, or a related discipline.
Minimum of 7 years of supply chain planning experience.
Hands-on experience with SAP IBP, supply planning processes, and SAP master data management.
Experience supporting production planning, inventory planning, capacity planning, and demand-supply balancing activities.
Strong analytical, problem-solving, and cross-functional collaboration skills.
Advanced proficiency in Excel and planning/reporting tools.
Experience within pharmaceutical, biotechnology, life sciences, or other regulated manufacturing environments.
Familiarity with Sales &amp; Operations Execution (S&amp;OE), Integrated Business Planning (IBP), and Supply Review processes.
Experience supporting clinical and commercial manufacturing supply chains.
Knowledge of planning metrics, dashboard development, and supply chain performance reporting.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $60.00 - $67.00/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)Workplace TypeThis is a fully onsite position in Cambridge,MA.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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.

public

Sap Analyst

Job Title: SchedulerJob DescriptionWe are seeking a dedicated Scheduler to join our team in supporting ongoing projects in Boise, ID. The position offers the flexibility of working on-site at the Micron project in Boise or from the Portland office.Responsibilities<ul><li>Provide ongoing schedule tracking and labor projections for multiple projects using standardized company workbooks.</li><li>Develop large project and specific area micro schedules using Microsoft Project or P6.</li><li>Resource load project schedules with labor hours.</li><li>Regularly update and maintain project schedules, labor analysis tools, and track actual hours worked.</li><li>Coordinate with the construction team to update schedules for each project.</li><li>Develop impact and multiple scenario schedules.</li><li>Perform additional duties as assigned.</li></ul>Essential Skills<ul><li>2+ years of experience in a Scheduler position within the construction industry.</li><li>Proficiency in Microsoft Office Suite and Microsoft Project.</li><li>Ability to read, interpret, and analyze construction schedules.</li><li>Advanced knowledge of construction scheduling.</li><li>Excellent human relations skills and ability to maintain confidentiality.</li><li>Excellent oral and written communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Expereince in electrical subcontractor construction.</li><li>Experience supporting data center projects.</li><li>Two-year technical or business degree.</li></ul>Work EnvironmentThis position offers a dynamic work environment with the opportunity to work on-site at the Micron project in Boise, ID, operating on a 60/60/50 schedule. A company phone or allowance is provided, and relocation assistance is available for the right candidate. The role is salaried and part of a strong company culture. Benefits include medical, dental, and vision insurance, with stipends available if covered by a spouse. The company also provides term life insurance, AD&amp;D coverage, a 401k retirement plan with up to a 10% employer match, and PTO accrual of up to 3 weeks, which can be used immediately. The role also includes 7 company-paid holidays.Job Type &amp; LocationThis is a Permanent position based out of Boise, ID.Pay and BenefitsThe pay range for this position is $85000.00 - $100000.00/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.Company culture is very strong
Medical, dental, and vision insurance - if they are covered by spouse company will still pay them a stipend
Company paid term life insurance and AD&amp;D coverage
401k retirement plan with employer match and company contribution - up to 10% match
PTO accrual of up to 3 weeks, but can start using it right away 
7 company paid holidaysWorkplace TypeThis is a fully onsite position in Boise,ID.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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.

Scheduler

Job Title: SchedulerJob DescriptionThe Scheduler develops, maintains, and analyzes detailed project schedules to support complex engineering and construction initiatives. This role creates cost-loaded, resource-loaded, and logic-driven schedules, ensures accurate schedule and cost data throughout the project lifecycle, and delivers clear status reporting to project teams. The Scheduler also plays a key role in mentoring and training less experienced schedulers, contributing to the continuous improvement of project control standards and practices.Responsibilities<ul><li>Develop, maintain, and analyze comprehensive project schedules for assigned projects, ensuring they are cost-loaded, resource-loaded, and logic-driven.</li><li>Manage all project schedule and cost-related updates throughout the lifecycle of each project to keep information current and accurate.</li><li>Interface regularly with engineering, construction, planning, project management, and other transmission partners to verify schedule, resource, and cost information.</li><li>Lead project schedule baseline review meetings with team members to confirm assumptions, dependencies, and resource allocations.</li><li>Analyze project progress and provide recommendations on forecasted costs based on schedule performance and trends.</li><li>Maintain estimated project costs within the designated scheduling and project controls systems.</li><li>Perform final project assessments to ensure compliance with established project control group standards.</li><li>Assist in developing metrics and measures for the transmission engineering and project services (TE&amp;PS) project portfolio.</li><li>Participate in the development and refinement of project control standards, guidelines, and best practices.</li><li>Ensure planning, engineering, construction, and project management teams are following established project lifecycle management processes (PLMP).</li><li>Mentor and train less experienced schedulers to build team capability and consistency in scheduling practices.</li></ul>Essential Skills<ul><li>Eight years of experience in scheduling or project controls within a construction environment.</li><li>Eight years of experience interfacing with engineering, construction, planning, and project management teams on project delivery.</li><li>Strong proficiency in scheduling tools and project controls systems used for cost-loaded and resource-loaded schedules.</li><li>Demonstrated ability to analyze project progress and develop accurate cost forecasts.</li><li>Proven experience leading schedule baseline review meetings and collaborating with cross-functional stakeholders.</li><li>Ability to perform final project assessments and ensure compliance with established standards and guidelines.</li><li>Strong analytical skills with the ability to interpret schedule data, cost information, and performance metrics.</li><li>Effective communication skills to present schedule status, issues, and recommendations to project teams.</li><li>Ability to mentor and train less experienced schedulers, sharing best practices and standard methodologies.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate or Bachelor’s Degree (ABET) in Construction Management, Engineering, Accounting, or Business.</li><li>Experience contributing to the development of project control standards and guidelines.</li><li>Background in developing metrics and measures for project portfolios, particularly in engineering or transmission-related projects.</li><li>Familiarity with project lifecycle management processes and adherence to standardized procedures.</li><li>Experience working in an engineering-focused environment with multi-disciplinary project teams.</li></ul>Work EnvironmentThis role operates in a quiet engineering office environment that supports focused, analytical work. The dress code is business casual. Teamwork is highly encouraged and occurs frequently, with regular collaboration among engineering, construction, planning, and project management teams. The position involves working with scheduling and project control technologies and systems to manage cost and resource data, and requires comfort in a structured, process-driven setting where established standards and guidelines are followed.Job Type &amp; LocationThis is a Permanent position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $31.25 - $35.10/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)Workplace TypeThis is a hybrid position in Tulsa,OK.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of New Albany, OH.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in New Albany,OH.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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: SchedulerJob DescriptionWe are seeking a dedicated Scheduler to join our team in supporting ongoing projects in Boise, ID. The position offers the flexibility of working on-site at the Micron project in Boise or from the Portland office.Responsibilities<ul><li>Provide ongoing schedule tracking and labor projections for multiple projects using standardized company workbooks.</li><li>Develop large project and specific area micro schedules using Microsoft Project or P6.</li><li>Resource load project schedules with labor hours.</li><li>Regularly update and maintain project schedules, labor analysis tools, and track actual hours worked.</li><li>Coordinate with the construction team to update schedules for each project.</li><li>Develop impact and multiple scenario schedules.</li><li>Perform additional duties as assigned.</li></ul>Essential Skills<ul><li>2+ years of experience in a Scheduler position within the construction industry.</li><li>Proficiency in Microsoft Office Suite and Microsoft Project.</li><li>Ability to read, interpret, and analyze construction schedules.</li><li>Advanced knowledge of construction scheduling.</li><li>Excellent human relations skills and ability to maintain confidentiality.</li><li>Excellent oral and written communication skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Expereince in electrical subcontractor construction.</li><li>Experience supporting data center projects.</li><li>Two-year technical or business degree.</li></ul>Work EnvironmentThis position offers a dynamic work environment with the opportunity to work on-site at the Micron project in Boise, ID, operating on a 60/60/50 schedule. A company phone or allowance is provided, and relocation assistance is available for the right candidate. The role is salaried and part of a strong company culture. Benefits include medical, dental, and vision insurance, with stipends available if covered by a spouse. The company also provides term life insurance, AD&amp;D coverage, a 401k retirement plan with up to a 10% employer match, and PTO accrual of up to 3 weeks, which can be used immediately. The role also includes 7 company-paid holidays.Job Type &amp; LocationThis is a Permanent position based out of Boise, ID.Pay and BenefitsThe pay range for this position is $85000.00 - $100000.00/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.Company culture is very strong
Medical, dental, and vision insurance - if they are covered by spouse company will still pay them a stipend
Company paid term life insurance and AD&amp;D coverage
401k retirement plan with employer match and company contribution - up to 10% match
PTO accrual of up to 3 weeks, but can start using it right away 
7 company paid holidaysWorkplace TypeThis is a fully onsite position in Boise,ID.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of Nashville, TN.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Nashville,TN.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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.

<h1>Job Description</h1>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.Job Type &amp; LocationThis is a Contract to Hire position based out of Atlanta, GA.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Atlanta,GA.Application DeadlineThis position is anticipated to close on Sep 17, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of Kansas City, MO.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Kansas City,MO.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of Columbus, OH.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Columbus,OH.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of Austin, TX.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Austin,TX.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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: Plant Production Scheduling Coordinator M-F day shiftLong term opportunity to grow within companyJob DescriptionThe Plant Production Scheduling Coordinator is responsible for coordinating production scheduling activities at the plant, with a focus on quality assurance and accurate documentation. This role ensures the accuracy and efficiency of production workflows by managing batch scheduling, maintaining labeling and production supplies, updating key performance indicators (KPIs), and keeping all records and filing current. The coordinator works closely with labeling personnel and production teams to ensure labels are correct, production plans are clear, and operations run smoothly and efficiently.Responsibilities<ul><li>Coordinate production scheduling activities for the plant to support efficient and timely manufacturing execution.</li><li>Review and validate total demand requirements for product batches to determine optimal batch sizes and proper warehouse allocation.</li><li>Generate and issue batch tickets as required to support manufacturing execution and ensure production teams have accurate instructions.</li><li>Respond to informal product requests from authorized approval sources, prioritizing batches and providing visibility into production status.</li><li>Determine manufacturing resource requirements, including materials, labor, and equipment, and schedule these resources for optimal utilization.</li><li>Review resource constraints such as material availability, labor capacity, and equipment readiness, and adjust production schedules accordingly while considering contingency plans.</li><li>Notify appropriate parties when schedules need modification, especially when changes may affect customer promise dates.</li><li>Verify all production batch tickets for accuracy of allocations and notify relevant departments to correct any discrepancies.</li><li>Input daily information for completed production batches into spreadsheets to monitor batch-specific information and downtime key performance indicators (KPIs).</li><li>Maintain and update plant KPI data to support performance tracking and continuous improvement initiatives.</li><li>Maintain and order production and labeling supplies to ensure uninterrupted operations and accurate labeling.</li><li>Work with labeling personnel to ensure all labels are correct, compliant, and printed properly for each production batch.</li><li>Keep the production planning board in good order, ensuring it accurately reflects current schedules and priorities.</li><li>Keep all filing and documentation up to date, including production records, batch tickets, and related administrative documents.</li><li>Provide backup support to the Administrative Assistant as needed to ensure continuity of administrative functions.</li><li>Participate in Total Quality and ERP processes, supporting system updates, data accuracy, and process adherence.</li><li>Take an active role in hazard recognition and injury prevention by following all safety rules and regulations and reporting all injuries and incidents to a supervisor.</li><li>Follow all environmental rules and regulations to ensure hazardous materials and waste are managed in an environmentally responsible manner.</li><li>Demonstrate commitment to the company’s safety and quality programs by consistently following established policies and procedures.</li><li>Perform other duties and assignments as directed by management to support plant operations and business needs.</li></ul>Essential Skills<ul><li>High School Diploma or equivalent experience.</li><li>Experience using Microsoft Office applications.</li><li>Proficiency in Microsoft Excel for data entry, tracking, and reporting of production batches and KPIs.</li><li>Strong problem-solving skills and the ability to address issues related to scheduling, resources, and documentation.</li><li>Ability to read and interpret documents such as procedure manuals, operating and maintenance manuals, and safety rules.</li><li>Ability to use a computer for all required company processes, procedures, and training.</li><li>Attention to detail and accuracy when reviewing batch tickets, labels, and production documentation.</li><li>Ability to coordinate multiple tasks and priorities in a production environment.</li><li>Strong communication skills to collaborate effectively with production teams, labeling personnel, and other departments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in production planning or coordination in an industrial or manufacturing environment.</li><li>Familiarity with ERP systems and participation in Total Quality and ERP processes.</li><li>Experience working with labeling processes and documentation control.</li><li>Comfort working with KPI tracking and performance metrics.</li><li>Organizational skills to maintain up-to-date filing systems and production records.</li></ul>Work EnvironmentThis role operates in an industrial-type work environment within a plant setting. The position requires extensive computer usage for up to 8 hours per day, with most tasks performed at a workstation or office area within the facility. The role involves regular interaction with production areas, labeling personnel, and other plant staff, and may require moving between office and production floor environments. There are no unusual environmental, lifting, or exertion requirements associated with this position, but adherence to all plant safety and environmental rules is essential. The coordinator works within a structured environment that emphasizes safety, quality, accurate documentation, and effective use of production resources.Job Type &amp; LocationThis is a Contract position based out of Dayton, NV.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)Workplace TypeThis is a fully onsite position in Dayton,NV.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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.

<h1>Scheduler</h1><h2>Help Deliver Complex Construction Projects</h2>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.<h3>Why Join Us?</h3><ul><li>Work on high-profile data center and mission-critical projects.</li><li>Gain experience on complex, large-scale construction programs.</li><li>Collaborate with experienced project controls and construction professionals.</li><li>Excellent opportunity for career growth in scheduling and project controls.</li><li>12-month contract-to-hire opportunity with PTO, paid holidays, and travel benefits.</li></ul>If you're a Primavera P6 Scheduler looking to make an impact on some of the country's most challenging construction projects, we'd love to hear from you.Job Type &amp; LocationThis is a Contract to Hire position based out of Atlanta, GA.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Atlanta,GA.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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.

<h1>Job Description</h1>We're seeking a Scheduler to support large-scale construction projects, including mission-critical and data center facilities. In this role, you'll partner with project managers, field teams, and stakeholders to develop and maintain project schedules that drive successful project execution from planning through completion.<h3>What You'll Do</h3><ul><li>Develop, maintain, and analyze project schedules using Primavera P6.</li><li>Partner with project teams to track progress, identify risks, and develop solutions to keep projects on schedule.</li><li>Conduct regular site visits to evaluate project status and improve construction sequencing.</li><li>Prepare schedule updates, forecasts, and progress reports for project leadership.</li><li>Support Pull Planning, Lean construction initiatives, and project pursuit activities.</li><li>Collaborate with operations, project controls, and business development teams to support successful project delivery.</li></ul><h3>What We're Looking For</h3><ul><li>3-5 years of construction scheduling experience.</li><li>Proficiency with Primavera P6 and Microsoft Office.</li><li>Knowledge of CPM scheduling, construction sequencing, and project controls.</li><li>Ability to read and interpret construction drawings and specifications.</li><li>Strong communication, analytical, and organizational skills.</li><li>Experience supporting mission-critical, industrial, or data center projects is a plus.</li></ul><h3>Work Environment &amp; Travel</h3>This role combines office-based work with regular field visits to active construction sites. Candidates should be comfortable working in both office and construction environments, including occasional exposure to varying weather conditions during site visits.Travel is required and may include assignments supporting projects in locations such as Kansas City, MO; Bowling Green, OH; El Paso, TX; Nashville, TN; and Atlanta, GA. Projects are typically long-term and may last 2-3 years. Travel expenses, project relocation costs, per diem, and periodic trips home are provided in accordance with company travel policies.Job Type &amp; LocationThis is a Contract to Hire position based out of Kansas City, MO.Pay and BenefitsThe pay range for this position is $43.27 - $57.69/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)Workplace TypeThis is a fully onsite position in Kansas City,MO.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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.

<h2>Scientific Technician</h2><h3>About the Role</h3>We are seeking a Scientific Technician to support laboratory testing and donor processing operations. This role is responsible for performing analytical testing, operating laboratory equipment, documenting results, and maintaining compliance with quality and regulatory standards. This is an excellent opportunity for recent science graduates looking to start a career in laboratory operations, healthcare, or biomanufacturing.<h3>Responsibilities</h3><ul><li>Perform donor suitability testing and routine laboratory assays</li><li>Conduct analytical testing using manual and automated methods</li><li>Analyze, document, and review test results</li><li>Operate, calibrate, troubleshoot, and maintain laboratory equipment</li><li>Complete quality control activities and preventative maintenance procedures</li><li>Manage sample workflow and test data using laboratory information systems</li><li>Follow cGMP, regulatory, safety, and environmental requirements</li><li>Collaborate with laboratory and cross-functional teams to support daily operations</li></ul><h3>Qualifications</h3>Required:<ul><li>Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology, or a related scientific field</li><li>Strong computer skills</li><li>Excellent communication and organizational abilities</li><li>Strong attention to detail and ability to follow procedures</li></ul>Preferred:<ul><li>MLT or MT certification</li><li>Tennessee laboratory licensure</li><li>2+ years of laboratory experience</li></ul><h3>Schedule</h3><ul><li>Monday through Friday</li><li>2:00 PM - 10:30 PM</li></ul><h3>Work Environment</h3><ul><li>Laboratory and office setting within a donor processing facility</li><li>Hands-on work with analytical instruments and laboratory information systems</li><li>Focus on quality, compliance, and safety standards</li></ul>Join a growing organization where you can gain valuable laboratory experience and build a long-term career in the healthcare and life sciences industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Knoxville, TN.Pay and BenefitsThe pay range for this position is $21.00 - $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)Workplace TypeThis is a fully onsite position in Knoxville,TN.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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.

Scientific Technician

<h1>Scientific Technician</h1><h2>Position Overview</h2>We are seeking a Scientific Technician to join a donor processing and manufacturing facility. This role is responsible for performing laboratory testing, operating analytical equipment, maintaining quality standards, and ensuring compliance with cGMP and regulatory requirements. This is an excellent opportunity for recent science graduates looking to enter the medical and laboratory field with a company that offers strong training and career growth opportunities.<h2>Responsibilities</h2><ul><li>Perform and troubleshoot donor suitability testing and other laboratory assays.</li><li>Conduct routine analytical testing using manual and automated methods.</li><li>Analyze and document test results against established controls.</li><li>Operate, calibrate, troubleshoot, and maintain laboratory instruments and equipment.</li><li>Complete Quality Control (QC) activities and preventative maintenance according to SOPs.</li><li>Use laboratory information systems to manage sample workflow and test data.</li><li>Maintain compliance with cGMP, regulatory, and safety requirements.</li><li>Follow Health, Safety &amp; Environmental (HSE) policies and procedures.</li><li>Collaborate with laboratory personnel and cross-functional teams to resolve issues and support operations.</li></ul><h2>Shift:</h2><ul><li>Monday - Friday</li><li>2:00PM - 10:30PM</li></ul><h2>Qualifications</h2><h3>Required</h3><ul><li>Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology, or a related scientific field.</li><li>Strong computer skills.</li><li>Excellent communication and organizational skills.</li><li>Strong attention to detail and ability to follow procedures.</li></ul><h3>Preferred</h3><ul><li>Medical Laboratory Technician (MLT) or Medical Technologist (MT) certification.</li><li>Tennessee laboratory licensure.</li><li>2+ years of laboratory experience.</li></ul><h2>Why Join?</h2><ul><li>Open to recent graduates.</li><li>Comprehensive training provided.</li><li>No on-call responsibilities.</li><li>Competitive benefits package.</li><li>Tuition reimbursement.</li><li>Career growth opportunities within a global organization.</li><li>Supportive and team-oriented work environment.</li></ul><h2>Work Environment</h2>This position is based in a laboratory and office environment within a donor processing facility. Employees work with analytical instruments, laboratory information systems, and regulated processes while following established quality and safety standards.Ideal candidates will have a scientific experience, strong attention to detail, and an interest in building a career in laboratory operations, healthcare, or biomanufacturing.Job Type &amp; LocationThis is a Contract position based out of Knoxville, TN.Pay and BenefitsThe pay range for this position is $21.00 - $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)Workplace TypeThis is a fully onsite position in Knoxville,TN.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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: ScientistResponsibilities<ul><li>Identify and recommend improvements to laboratory and production processes to maintain and enhance quality, cost effectiveness, safety compliance, and other key performance parameters.</li><li>Perform timely release testing on all incoming raw materials required for manufacturing and on finished goods, ensuring results meet established specifications and timelines.</li><li>Coordinate the scheduling of all materials testing to meet company production and delivery requirements.</li><li>Ensure assigned products consistently meet quality requirements for both customers and the organization.</li><li>Draft clear, accurate written reports detailing the results of testing and analytical evaluations.</li><li>Approve the release of raw materials and finished goods based on analytical data and quality standards.</li><li>Proactively identify trends in laboratory analyses or functions, implement improvements, and communicate findings and recommendations to management.</li><li>Perform operations to support contract manufacturing organizations (CMOs) as necessary, including testing and documentation activities.</li><li>Operate and maintain laboratory equipment, identify issues when equipment fails, and conduct or recommend appropriate repairs.</li><li>Perform routine maintenance and calibration of laboratory equipment as needed to ensure accuracy and reliability.</li><li>Conduct peer review of analytical results generated by colleagues to ensure data integrity and compliance with procedures.</li><li>Perform peer review of test methods and protocols to confirm accuracy, clarity, and regulatory alignment.</li><li>Review and draft standard operating procedures (SOPs) as needed to reflect current practices and regulatory expectations.</li><li>Author and execute written protocols, including installation qualification and operational qualification (IQ/OQ) documents, as needed.</li><li>Cross-train to perform sample laboratory duties adequately and accurately, supporting flexibility and coverage within the team.</li><li>Lead and support audit-related activities in the lab, including preparation, execution, and follow-up of internal and external audits.</li><li>Collaborate with all levels of management and external vendors to support quality, compliance, and continuous improvement initiatives.</li><li>Manage multiple tasks and projects in a high-paced environment while consistently meeting deadlines and quality expectations.</li></ul>Essential Skills<ul><li>Expert-level knowledge and hands-on experience with HPLC or UPLC techniques.</li><li>Strong background in chemistry, analytical chemistry, wet chemistry, and laboratory operations.</li><li>Experience in quality control within a regulated laboratory or manufacturing environment.</li><li>Practical experience with audit management and audit support activities.</li><li>Thorough understanding of FDA regulations, FDA compliance, and current Good Manufacturing Practices (cGMP).</li><li>Strong verbal and written communication skills with the ability to work effectively with all levels of management and external vendors.</li><li>Proficiency with SAP Business One or similar enterprise resource planning software.</li><li>Working knowledge of scientific instrumentation and techniques relevant to analytical and quality control laboratories.</li><li>Working knowledge of regulatory, cGMP, and FDA regulations necessary to ensure products and production units meet quality standards.</li><li>Proficient computer skills, including basic spreadsheet functions and word processing.</li><li>Bachelor of Science degree in Chemistry, Microbiology, Biology, or a closely related scientific discipline.</li><li>At least 2 years of leadership experience, which may include leading projects, coordinating teams, and successfully meeting project deadlines.</li></ul>Work EnvironmentThis role is primarily based in a laboratory setting within a larger production facility. You will work around the lab and throughout the facility, supporting audits and preparing and managing FDA-related documentation. The environment is fast-paced and can be time-sensitive, requiring focus, adaptability, and careful adherence to safety and quality procedures. You will regularly use scientific instrumentation such as HPLC or UPLC systems and other analytical equipment, as well as computer systems including Microsoft Office, virtual meeting tools, and SAP Business One. The position involves close collaboration with laboratory colleagues, quality and regulatory teams, and other functional groups to maintain compliant, efficient, and well-documented operations.Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Pay and BenefitsThe pay range for this position is $28.00 - $32.00/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)Workplace TypeThis is a fully onsite position in Omaha,NE.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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.

Scientist

Job Title: Analytical Development ScientistJob DescriptionThis role focuses on supporting process development teams through advanced analytical testing and assay development in a fast-paced laboratory environment. The scientist performs complex analytical methods, generates and interprets data, troubleshoots issues, and ensures that results reliably support product development and GMP manufacturing decisions for vaccine and therapeutic products.Responsibilities<ul><li>Perform analytical assay development and characterization work to support vaccine and therapeutic product programs.</li><li>Support process development efforts by designing, executing, and refining analytical testing strategies.</li><li>Develop, optimize, and qualify analytical testing methods to ensure robust, reproducible data.</li><li>Run complex liquid chromatography and related analytical techniques, including HPLC, UPLC, reverse phase chromatography, size exclusion chromatography (SEC), lipid content analysis, and mass spectrometry (MS) where applicable.</li><li>Support formulation development and characterization activities by providing analytical data and method expertise.</li><li>Conduct GMP testing and lot release testing in accordance with established quality and regulatory standards.</li><li>Analyze data, interpret results, and troubleshoot analytical issues to resolve problems and improve methods.</li><li>Prepare and maintain clear, accurate technical reports, protocols, and GMP documentation.</li><li>Present analytical findings and recommendations to cross-functional teams in a clear and concise manner.</li><li>Collaborate closely with Process Development, Quality, Manufacturing, and Operations teams to align analytical strategies with development and production needs.</li><li>Work independently in the laboratory while managing a high volume of testing and supporting multiple internal functions simultaneously.</li><li>Ensure all laboratory activities adhere to applicable procedures, quality standards, and regulatory expectations.</li></ul>Essential Skills<ul><li>Bachelor's degree in a scientific discipline such as Biology, Biochemistry, Chemistry, Pharmaceutical Sciences, Engineering, or a related field.</li><li>At least 6 years of experience as an Analytical Development Scientist.</li><li>At least 6 years of experience developing and executing liquid chromatography methods, including reverse phase chromatography, size exclusion chromatography (SEC), and lipid content analysis.</li><li>Demonstrated proficiency in analytical method development, optimization, and qualification.</li><li>Strong analytical problem-solving abilities and experience troubleshooting complex assays.</li><li>Proven ability to work independently in a laboratory setting while managing a high testing volume.</li><li>Proficiency with Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.</li><li>Experience supporting process development activities through analytical testing in a biopharmaceutical or related environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>GMP experience, including GMP testing and lot release testing.</li><li>Hands-on experience with mass spectrometry (MS) techniques.</li><li>Formulation development and characterization experience.</li><li>Prior experience in biologics, vaccines, cell therapy, gene therapy, or pharmaceutical product development.</li><li>Background in analytical development within a biopharmaceutical, vaccine, or advanced therapeutics environment.</li><li>Experience supporting process development in a regulated setting.</li><li>Knowledge of federal compliance and sponsored project management gained through exposure to complex research programs.</li><li>Interest in mission-driven science focused on next-generation vaccines and emerging cancer vaccine platforms.</li><li>Motivation to grow through structured training, certifications, and professional development opportunities.</li><li>Ability to thrive in a collaborative, high-performing culture that values communication and shared problem-solving.</li></ul>Work EnvironmentThe position is based in a fast-paced GMP testing laboratory operating Monday through Friday from 8:00 AM to 5:00 PM. The environment centers on high-complexity analytical work supporting vaccine and therapeutic product development, with extensive use of HPLC, UPLC, reverse phase and size exclusion chromatography, lipid analysis, and mass spectrometry. Team members collaborate closely with scientists, faculty, and administrators across Process Development, Quality, Manufacturing, and Operations. The broader research setting offers access to large-scale, federally funded programs, multi-institutional collaborations, and sophisticated research administration systems. The culture emphasizes mission-driven science with global impact, combining the stability and infrastructure of a major research institution with the agility of an innovative, vaccine-focused center, and provides opportunities for ongoing learning, professional development, and participation in shaping future cancer vaccine initiatives.Job Type &amp; LocationThis is a Contract position based out of Durham, NC.Pay and BenefitsThe pay range for this position is $38.33 - $47.91/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)Workplace TypeThis is a fully onsite position in Durham,NC.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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: ScientistJob DescriptionThe Scientist plays a key role in ensuring product quality, regulatory compliance, and operational efficiency within a laboratory and manufacturing environment. This position focuses on analytical testing of raw materials and finished goods, continuous process improvement, support for audits and FDA-related documentation, and leadership within the laboratory and audit space.Responsibilities<ul><li>Identify and recommend improvements to laboratory and production processes to maintain quality, cost effectiveness, safety compliance, and other performance parameters.</li><li>Perform timely release testing on all incoming raw materials required for manufacturing and on finished goods, ensuring results are accurate and documented.</li><li>Coordinate the scheduling of all materials to meet internal production and quality requirements.</li><li>Ensure that assigned products consistently meet quality requirements for both customers and the organization.</li><li>Draft clear, written reports detailing the results of testing and analytical activities.</li><li>Approve the release of raw materials and finished goods based on established quality standards and test results.</li><li>Proactively identify trends in laboratory analysis and operations, implement improvements, and communicate findings and recommendations to management.</li><li>Perform operations in support of contract manufacturing organizations (CMOs) as needed.</li><li>Operate and maintain laboratory equipment, identify issues when equipment fails, and conduct or recommend appropriate repairs.</li><li>Perform routine maintenance and calibration of laboratory instruments and equipment as required.</li><li>Conduct peer review of analytical results generated by colleagues to ensure accuracy and compliance with procedures.</li><li>Perform peer review of test methods and protocols to maintain robust and reliable analytical practices.</li><li>Review and draft standard operating procedures (SOPs) as needed to align documentation with current procedures and regulatory expectations.</li><li>Author and execute written protocols, including IQOQ (Installation Qualification/Operational Qualification) documentation, as required.</li><li>Cross-train to competently perform sample laboratory duties accurately and efficiently.</li><li>Support audits and audit-related activities by providing laboratory data, documentation, and subject matter expertise on quality and compliance.</li></ul>Essential Skills<ul><li>Strong background in Chemistry, Biology, or related scientific discipline with practical laboratory experience.</li><li>Expert-level proficiency with HPLC or UPLC techniques for analytical testing.</li><li>Hands-on experience in analytical chemistry and wet chemistry within a quality control or laboratory environment.</li><li>Demonstrated experience in laboratory operations, including sample handling, testing, and documentation.</li><li>Excellent organizational skills and strong attention to detail to manage multiple tests, reports, and compliance requirements.</li><li>Excellent time management skills with a proven ability to meet deadlines in a fast-paced setting.</li><li>Strong verbal and written communication skills with the ability to collaborate effectively with all levels of management and external vendors.</li><li>Strong analytical and problem-solving skills, including the ability to read and understand technical instructions and materials in English.</li><li>Ability to function effectively in a high-paced and sometimes stressful environment while maintaining accuracy and composure.</li><li>Thorough understanding of FDA regulations and cGMP compliance requirements.</li><li>Working knowledge of regulatory expectations and quality standards to ensure products and production units meet required specifications.</li><li>Proficiency with Microsoft Office Suite and virtual meeting applications.</li><li>Experience using SAP Business One or similar enterprise resource planning software.</li><li>Proficient computer skills, including basic spreadsheet functions and word processing.</li><li>Working knowledge of scientific instrumentation and techniques relevant to analytical and quality control laboratories.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor of Science degree in Chemistry, Microbiology, Biology, or a closely related scientific field.</li><li>Experience supporting audits and audit management activities within a laboratory or manufacturing environment.</li><li>Experience providing audit support and preparing documentation for regulatory inspections.</li><li>Familiarity with FDA compliance documentation and processes.</li><li>Ability to act as a senior individual contributor and informal leader within the laboratory and audit space.</li><li>Comfort working with vendors and cross-functional teams to resolve quality and compliance issues.</li><li>Ability to contribute to continuous improvement initiatives and drive enhancements in laboratory efficiency and data integrity.</li></ul>Work EnvironmentThis role is primarily based in a laboratory setting and involves regular movement throughout the facility to support audits and FDA-related documentation. The Scientist works closely with production, quality, and regulatory teams, operating and maintaining scientific instrumentation and computer systems. The environment is fast-paced and may be stressful at times due to deadlines and audit activities, requiring consistent attention to detail and adherence to cGMP and FDA regulations. Standard laboratory safety practices and appropriate lab attire are expected while performing duties.Job Type &amp; LocationThis is a Contract to Hire position based out of Omaha, NE.Pay and BenefitsThe pay range for this position is $28.00 - $32.00/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)Workplace TypeThis is a fully onsite position in Omaha,NE.Application DeadlineThis position is anticipated to close on Sep 11, 2026.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: Scientist / Principal Associate Scientist – AAV Libraries &amp; Tissue-Based AnalyticsJob DescriptionThis role focuses on the design, generation, and selection of AAV libraries and the comprehensive analysis of tissue samples to evaluate vector biodistribution, transduction efficiency, and target cell engagement. You will optimize and execute tissue collection, processing, and downstream analytical workflows for both in vitro and in vivo studies to support the identification and selection of lead therapeutic candidates for translation to humans. The position is ideal for someone who enjoys hands-on work with tissues and mammalian cell culture, as well as AAV library preparation, and who is motivated to contribute to patient-focused therapeutic development.Responsibilities<ul><li>Contribute to the design, generation, and selection of AAV libraries to support discovery and translational development programs.</li><li>Process and evaluate tissue samples to assess vector biodistribution, transduction efficiency, and target cell engagement across multiple tissues and cell types.</li><li>Optimize and execute tissue collection, processing, and downstream analytical workflows for both in vitro and in vivo studies to enable selection of lead therapeutic candidates.</li><li>Perform tissue dissociation, nucleic acid extraction, and quantitative assessments of vector genomes, mRNA, and protein expression to characterize therapeutic performance and biological activity.</li><li>Utilize advanced tissue-based analytical techniques, including antibody-based imaging and FISH methodologies, to evaluate biodistribution, transgene expression, cellular localization, and target engagement in complex tissue specimens.</li><li>Develop, optimize, and troubleshoot tissue processing workflows to support high-throughput analysis of diverse tissue types while ensuring high data quality and reproducibility.</li><li>Rapidly process large numbers of tissue samples for DNA, RNA, and cell-based analyses in alignment with program timelines and project milestones.</li><li>Collaborate closely within the Molecular Therapeutics Department and across the broader R&amp;D organization to integrate tissue-derived data and biological insights into therapeutic candidate selection and advancement.</li><li>Apply molecular biology and quantitative analytical techniques to interpret experimental results and support data-driven decision making.</li><li>Contribute to maintaining accurate documentation of experiments, protocols, and results using appropriate informatics tools and laboratory systems.</li><li>Participate in troubleshooting, problem-solving, and continuous improvement of laboratory methods, workflows, and analytical strategies.</li><li>Engage with cross-functional teams to communicate findings, share technical expertise, and support the progression of discovery and translational programs.</li></ul>Essential Skills<ul><li>Extensive hands-on experience with tissue culture and mammalian cell culture.</li><li>Demonstrated experience with AAV libraries, including their design, generation, and application in experimental workflows.</li><li>Strong proficiency in tissue collection, processing, and downstream analytical workflows from in vitro and in vivo studies.</li><li>Hands-on experience in tissue dissociation and nucleic acid extraction from diverse tissue types.</li><li>Proficiency in quantitative analysis of nucleic acids and proteins, including ddPCR, ELISA, and MSD.</li><li>Experience performing quantitative assessments of vector genomes, mRNA, and protein expression to characterize therapeutic performance.</li><li>Experience in molecular biology sufficient to design, execute, and interpret complex biological experiments.</li><li>Ability to develop, optimize, and troubleshoot tissue processing workflows to support high-throughput analysis.</li><li>Strong statistical analysis skills and experience using statistical software such as PRISM.</li><li>Proficiency with computing tools and databases including Endnote, BLAST, Ensembl, NCBI, Uniprot, UCSC, GTEx, Microsoft applications, and Benchling.</li><li>For Principal Associate Scientist: typically a minimum of 6+ years of related experience with a Bachelor’s degree, or 4+ years of experience with a Master’s degree.</li><li>For Scientist I: typically a minimum of 8+ years of related experience with a Bachelor’s degree, or 6+ years with a Master’s degree, or a PhD with 0+ years of experience.</li><li>Strong problem-solving skills with the ability to work both independently and collaboratively within cross-functional teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Hands-on experience in tissue collection, including from preclinical models.</li><li>Hands-on experience with dosing and tissue collection procedures in mouse models (desirable).</li><li>Experience applying antibody-based imaging and FISH methodologies to complex tissue specimens.</li><li>Familiarity with evaluating biodistribution, transgene expression, cellular localization, and target engagement in tissue-based assays.</li><li>Experience in high-throughput tissue and cell-based analyses, including handling large numbers of samples under tight timelines.</li><li>Strong organizational skills and attention to detail in experimental design, execution, and documentation.</li><li>Ability to interpret and integrate data from multiple molecular and tissue-based assays to support therapeutic candidate selection.</li><li>Interest in working within a patient-focused environment aimed at improving the daily lives of individuals living with serious diseases.</li></ul>Work EnvironmentThis is a fully onsite laboratory-based position, operating Monday through Friday from 9:00 a.m. to 5:00 p.m. You will work in a research and development environment that emphasizes hands-on tissue and mammalian cell culture, AAV library preparation, and advanced molecular and tissue-based analytical techniques. The role involves frequent handling of tissue samples from both in vitro and in vivo studies, including high-throughput processing of DNA, RNA, and cell-based assays. You will use a range of laboratory technologies and informatics tools, including ddPCR, ELISA, MSD, antibody-based imaging, FISH, PRISM, Benchling, and various bioinformatics databases and software platforms. The environment encourages close collaboration across the Molecular Therapeutics Department and broader R&amp;D teams, with a strong focus on scientific rigor, data quality, reproducibility, and patient-centered impact.Job Type &amp; LocationThis is a Contract position based out of Boston, MA.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/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)Workplace TypeThis is a fully onsite position in Boston,MA.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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: ScientistJob DescriptionWe are seeking a dedicated Scientist to support our analytical laboratory operations, focusing on HPLC/LC method transfers. The successful candidate will utilize the Empower chromatography data system to execute method transfer protocols, perform analytical testing, and document analytical data in a GMP-regulated environment.Responsibilities<ul><li>Execute HPLC/LC method transfer protocols using the Empower CDS.</li><li>Perform sample and reagent preparation, and conduct analytical testing activities.</li><li>Complete analytical runs, replicates, and protocol-defined verification testing.</li><li>Review chromatographic data to ensure results meet established acceptance criteria.</li><li>Document testing activities and results in compliance with GMP requirements.</li><li>Support method verification, report generation, and transfer documentation.</li><li>Complete required training for DEA-controlled substance handling and testing.</li><li>Assist with the implementation of additional analytical methods and laboratory expansion.</li><li>Support increased testing capacity through routine laboratory testing activities.</li><li>Collaborate with Quality Assurance, Development, IT, and site personnel for successful project execution.</li><li>Participate in laboratory status meetings and provide project updates.</li><li>Support final reporting, knowledge transfer, and project closeout activities.</li></ul>Essential Skills<ul><li>Hands-on HPLC/LC laboratory testing experience.</li><li>Experience with Empower chromatography data system.</li><li>Ability to execute analytical test methods following approved protocols and SOPs.</li><li>Experience in preparing samples, standards, mobile phases, and reagents.</li><li>Ability to review chromatographic data and interpret analytical results.</li><li>Understanding of method transfer, verification, and reproducibility requirements.</li><li>Experience in a GMP-regulated pharmaceutical or biotechnology environment.</li><li>Ability to maintain accurate laboratory documentation and data integrity.</li><li>Knowledge of laboratory investigations, deviations, and quality systems.</li><li>Ability to manage multiple testing priorities while ensuring high-quality execution.</li></ul>Additional Skills &amp; Qualifications<ul><li>Minimum 3 to 5 years of experience in pharmaceutical, biotechnology, or analytical laboratories.</li><li>Minimum 2+ years of hands-on HPLC/LC testing experience.</li><li>Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, or a related scientific discipline preferred.</li><li>Experience with DEA-controlled substance testing or willingness to complete qualifications preferred.</li><li>Experience supporting method transfer, method validation, or method verification projects preferred.</li><li>Knowledge of FDA GMP regulations and laboratory compliance requirements.</li><li>Proficiency with laboratory documentation systems and Microsoft Office applications.</li><li>Experience supporting laboratory scale-up, increased testing capacity, or new method implementation is a plus.</li></ul>Work EnvironmentThe position is onsite at a dedicated facility, offering a fast-paced laboratory environment with changing priorities. The work involves collaboration across multiple departments, ensuring a dynamic and supportive team atmosphere.Job Type &amp; LocationThis is a Contract position based out of Clinton, IN.Pay and BenefitsThe pay range for this position is $50.00 - $55.00/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)Workplace TypeThis is a fully onsite position in Clinton,IN.Application DeadlineThis position is anticipated to close on Sep 19, 2026.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: ScientistJob DescriptionThe Scientist will perform analytical testing on client samples using UV/Vis spectroscopy, filtration techniques, and microscopy in a regulated laboratory environment. This role focuses on generating high-quality data while ensuring all work complies with FDA regulations and cGMP standards. It is an excellent opportunity for professionals from pharmaceutical, medical device, biotech, contract testing, or other regulated laboratories who want to contribute to the expansion and build-out of a growing testing facility.Responsibilities<ul><li>Perform analytical laboratory testing on client samples by following established standard operating procedures (SOPs) and approved test methods.</li><li>Analyze samples using UV/Vis spectroscopy to generate accurate and reliable quantitative and qualitative data.</li><li>Conduct filtration testing, including membrane filtration, particulate evaluations, and related filter integrity assessments.</li><li>Use microscopy to examine and identify particles, contaminants, and key sample characteristics.</li><li>Record and review laboratory data in compliance with cGMP and Good Documentation Practices (GDP), ensuring data integrity and traceability.</li><li>Maintain accurate laboratory records and enter results into laboratory information management systems (LIMS) or electronic lab notebooks (ELN) when applicable.</li><li>Ensure all testing activities align with FDA and other relevant regulatory requirements and internal quality standards.</li><li>Prepare reagents, solutions, and standards needed for routine and specialized testing activities.</li><li>Maintain, calibrate, and troubleshoot laboratory equipment to support consistent and reliable operation.</li><li>Participate in investigations involving out-of-specification (OOS), out-of-trend (OOT) results, deviations, and other quality events.</li><li>Assist with updating SOPs and supporting audits, inspections, and continuous improvement initiatives within the laboratory.</li><li>Contribute to the ongoing expansion of testing services by supporting new methods, technologies, and process improvements as the laboratory grows.</li></ul>Essential Skills<ul><li>Bachelor’s degree in chemistry, biology, materials science, or a closely related scientific discipline.</li><li>1–3 years of hands-on laboratory experience in a GMP-regulated laboratory environment.</li><li>Industry experience performing UV/Vis spectroscopy for analytical testing.</li><li>Practical experience with filtration testing, including membrane filtration, particulate testing, and filter integrity testing.</li><li>Experience using microscopy to identify and characterize particles and contaminants in samples.</li><li>Familiarity with maintaining a lab notebook or working within an electronic lab notebook (ELN) system.</li><li>Working knowledge of cGMP requirements and Good Documentation Practices (GDP) in a regulated laboratory setting.</li><li>Ability to follow detailed SOPs and test methods accurately and consistently.</li><li>Strong attention to detail and commitment to data integrity and regulatory compliance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a contract testing laboratory environment.</li><li>Instrumentation experience with HPLC, FTIR, and particle sizing equipment.</li><li>Exposure to method validation or technology transfer activities within a regulated setting.</li><li>Prior experience authoring CAPA (Corrective and Preventive Action) investigations.</li><li>Familiarity with USP, EP, and ICH guidelines and understanding of FDA regulatory expectations.</li><li>Ability to support audits and contribute to continuous improvement initiatives in the laboratory.</li><li>Strong problem-solving skills and ability to participate effectively in OOS, OOT, and deviation investigations.</li></ul>Work EnvironmentThe role is based in a brand-new contract testing laboratory that focuses on supporting pharmaceutical and medical device clients. The team is in an early growth phase and is adding key roles to help build out the business and expand testing services. You will work with modern analytical instrumentation and laboratory systems in a cGMP-compliant environment, collaborating closely with other scientists and quality-focused professionals. The setting offers the opportunity to influence laboratory processes and contribute to a culture of continuous improvement and scientific excellence.Job Type &amp; LocationThis is a Contract to Hire position based out of Minnetonka, MN.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)Workplace TypeThis is a fully onsite position in Minnetonka,MN.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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: Scientist / Principal Associate Scientist – AAV Libraries &amp; Tissue-Based AnalyticsJob DescriptionThis role focuses on the design, generation, and selection of AAV libraries and the comprehensive analysis of tissue samples to evaluate vector biodistribution, transduction efficiency, and target cell engagement. You will optimize and execute tissue collection, processing, and downstream analytical workflows for both in vitro and in vivo studies to support the identification and selection of lead therapeutic candidates for translation to humans. The position is ideal for someone who enjoys hands-on work with tissues and mammalian cell culture, as well as AAV library preparation, and who is motivated to contribute to patient-focused therapeutic development.Responsibilities<ul><li>Contribute to the design, generation, and selection of AAV libraries to support discovery and translational development programs.</li><li>Process and evaluate tissue samples to assess vector biodistribution, transduction efficiency, and target cell engagement across multiple tissues and cell types.</li><li>Optimize and execute tissue collection, processing, and downstream analytical workflows for both in vitro and in vivo studies to enable selection of lead therapeutic candidates.</li><li>Perform tissue dissociation, nucleic acid extraction, and quantitative assessments of vector genomes, mRNA, and protein expression to characterize therapeutic performance and biological activity.</li><li>Utilize advanced tissue-based analytical techniques, including antibody-based imaging and FISH methodologies, to evaluate biodistribution, transgene expression, cellular localization, and target engagement in complex tissue specimens.</li><li>Develop, optimize, and troubleshoot tissue processing workflows to support high-throughput analysis of diverse tissue types while ensuring high data quality and reproducibility.</li><li>Rapidly process large numbers of tissue samples for DNA, RNA, and cell-based analyses in alignment with program timelines and project milestones.</li><li>Collaborate closely within the Molecular Therapeutics Department and across the broader R&amp;D organization to integrate tissue-derived data and biological insights into therapeutic candidate selection and advancement.</li><li>Apply molecular biology and quantitative analytical techniques to interpret experimental results and support data-driven decision making.</li><li>Contribute to maintaining accurate documentation of experiments, protocols, and results using appropriate informatics tools and laboratory systems.</li><li>Participate in troubleshooting, problem-solving, and continuous improvement of laboratory methods, workflows, and analytical strategies.</li><li>Engage with cross-functional teams to communicate findings, share technical expertise, and support the progression of discovery and translational programs.</li></ul>Essential Skills<ul><li>Extensive hands-on experience with tissue culture and mammalian cell culture.</li><li>Demonstrated experience with AAV libraries, including their design, generation, and application in experimental workflows.</li><li>Strong proficiency in tissue collection, processing, and downstream analytical workflows from in vitro and in vivo studies.</li><li>Hands-on experience in tissue dissociation and nucleic acid extraction from diverse tissue types.</li><li>Proficiency in quantitative analysis of nucleic acids and proteins, including ddPCR, ELISA, and MSD.</li><li>Experience performing quantitative assessments of vector genomes, mRNA, and protein expression to characterize therapeutic performance.</li><li>Experience in molecular biology sufficient to design, execute, and interpret complex biological experiments.</li><li>Ability to develop, optimize, and troubleshoot tissue processing workflows to support high-throughput analysis.</li><li>Strong statistical analysis skills and experience using statistical software such as PRISM.</li><li>Proficiency with computing tools and databases including Endnote, BLAST, Ensembl, NCBI, Uniprot, UCSC, GTEx, Microsoft applications, and Benchling.</li><li>For Principal Associate Scientist: typically a minimum of 6+ years of related experience with a Bachelor’s degree, or 4+ years of experience with a Master’s degree.</li><li>For Scientist I: typically a minimum of 8+ years of related experience with a Bachelor’s degree, or 6+ years with a Master’s degree, or a PhD with 0+ years of experience.</li><li>Strong problem-solving skills with the ability to work both independently and collaboratively within cross-functional teams.</li></ul>Additional Skills &amp; Qualifications<ul><li>Hands-on experience in tissue collection, including from preclinical models.</li><li>Hands-on experience with dosing and tissue collection procedures in mouse models (desirable).</li><li>Experience applying antibody-based imaging and FISH methodologies to complex tissue specimens.</li><li>Familiarity with evaluating biodistribution, transgene expression, cellular localization, and target engagement in tissue-based assays.</li><li>Experience in high-throughput tissue and cell-based analyses, including handling large numbers of samples under tight timelines.</li><li>Strong organizational skills and attention to detail in experimental design, execution, and documentation.</li><li>Ability to interpret and integrate data from multiple molecular and tissue-based assays to support therapeutic candidate selection.</li><li>Interest in working within a patient-focused environment aimed at improving the daily lives of individuals living with serious diseases.</li></ul>Work EnvironmentThis is a fully onsite laboratory-based position, operating Monday through Friday from 9:00 a.m. to 5:00 p.m. You will work in a research and development environment that emphasizes hands-on tissue and mammalian cell culture, AAV library preparation, and advanced molecular and tissue-based analytical techniques. The role involves frequent handling of tissue samples from both in vitro and in vivo studies, including high-throughput processing of DNA, RNA, and cell-based assays. You will use a range of laboratory technologies and informatics tools, including ddPCR, ELISA, MSD, antibody-based imaging, FISH, PRISM, Benchling, and various bioinformatics databases and software platforms. The environment encourages close collaboration across the Molecular Therapeutics Department and broader R&amp;D teams, with a strong focus on scientific rigor, data quality, reproducibility, and patient-centered impact.Job Type &amp; LocationThis is a Contract position based out of Boston, MA.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/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)Workplace TypeThis is a fully onsite position in Boston,MA.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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: Scientist IIJob DescriptionWe are seeking a Scientist II with expertise in chemistry and a strong understanding of HPLC and LC/MS. This contractor role will support PET tracer metabolite analysis and routine radiotracer production activities.Responsibilities<ul><li>Support the setup and optimization of HPLC systems for metabolite analysis of PET tracers.</li><li>Perform the daily operation of HPLC systems used for metabolite analysis.</li><li>Conduct routine PET radiotracer production activities.</li><li>Independently establish HPLC methods and ensure that systems are robust, reliable, and properly maintained.</li><li>Document experimental procedures, results, and laboratory activities in accordance with applicable standards.</li><li>Follow all relevant laboratory safety, quality, and compliance procedures.</li></ul>Essential Skills<ul><li>Bachelor's degree in chemistry or a related scientific discipline with at least five years of experience, or a Master's degree in chemistry or a related scientific discipline with at least three years of research experience.</li><li>Working knowledge of HPLC and LC/MS.</li><li>Ability to work independently and maintain laboratory systems effectively.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in PET radiochemistry.</li><li>Experience with setting up, optimizing, and maintaining HPLC systems.</li><li>Experience with radiotracer production or analytical characterization of PET tracers.</li></ul>Work EnvironmentThe work environment involves laboratory settings where you will utilize advanced technologies such as HPLC and LC/MS. You will independently manage systems and ensure compliance with safety and quality standards.Job Type &amp; LocationThis is a Contract position based out of North Chicago, IL.Pay and BenefitsThe pay range for this position is $50.00 - $55.00/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)Workplace TypeThis is a fully onsite position in North Chicago,IL.Application DeadlineThis position is anticipated to close on Sep 15, 2026.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.

Scientist II

<h1>Scientist II - Reagent &amp; Assay Development</h1>Location: Peachtree Corners, GA (On-Site)Pay Range: $43-$55/hr - will vary based on experience Type: Contract-to-Hire (6 Months)Schedule: Flexible start/end times between 7:00 AM - 6:00 PM<h2>Overview</h2>Seeking a Scientist II to join a leading biotechnology company specializing in immunohematology and transfusion medicine products. This role will support the development, optimization, characterization, and validation of diagnostic reagents and in-vitro assays used to improve patient care worldwide.This is an excellent opportunity for scientists with experience in assay development, immunology, immunohematology, immunoassays, or related laboratory research who are looking to contribute to innovative product development in a highly collaborative environment.<h2>Responsibilities</h2><ul><li>Design, plan, and execute laboratory experiments supporting reagent and assay development projects.</li><li>Analyze and interpret experimental data and communicate findings to cross-functional teams.</li><li>Perform studies involving antigen-antibody interactions, serologic methods, reagent characterization, and assay performance evaluation.</li><li>Support reagent formulation, assay optimization, stability studies, and product characterization activities.</li><li>Assist with verification, validation, and design transfer activities for new and existing products.</li><li>Investigate technical issues, troubleshoot laboratory challenges, and recommend corrective actions.</li><li>Maintain accurate laboratory documentation, protocols, technical reports, and experimental records.</li><li>Collaborate with R&amp;D, Quality, Regulatory, Clinical, and Manufacturing teams to support project objectives.</li><li>Contribute to continuous improvement initiatives and support product lifecycle activities.</li></ul><h2>Qualifications</h2><h3>Required:</h3><ul><li>Bachelor's degree in Biology, Immunology, Biochemistry, Biomedical Sciences, or a related scientific discipline with 4+ years of relevant experience.</li><li>OR Master's degree with 2+ years of relevant industry experience.</li><li>OR PhD with applicable research experience.</li><li>Experience with assay development and reagent development</li><li>Experience conducting laboratory experiments and analyzing scientific data - must have data analysis experience</li><li>Strong understanding of scientific methods and experimental design.</li><li>Excellent documentation, organization, and communication skills.</li></ul><h3>Preferred:</h3><ul><li>Experience with immunohematology, immunology, transfusion medicine, serology, or immunoassays.</li><li>Experience in medical device, biotechnology, diagnostics, or regulated laboratory environments.</li><li>Familiarity with verification, validation, and product development processes.</li><li>Knowledge of FDA, ISO, GMP, or quality system requirements.</li></ul><h2>Why Join?</h2><ul><li>Opportunity to work with cutting-edge diagnostic technologies.</li><li>Collaborative and innovative research environment.</li><li>Opportunity with long-term growth potential.</li><li>Flexible work schedule.</li><li>Holiday pay</li><li>Comprehensive benefits package including medical, dental, vision, 401(k), life insurance, and supplemental coverage options.</li></ul>Apply today to join a team developing innovative diagnostic solutions that make a difference in patient care around the world.<h3>Keywords for sourcing</h3>Scientist, Scientist II, Research Scientist, Associate Scientist, Sr Scientist, Immunologist, Immunohematology Scientist, Assay Development Scientist, R&amp;D Scientist, Immunoassay Scientist, Serology Scientist, Biochemistry Scientist, Transfusion Medicine Scientist, Medical Device Scientist, Biotechnology Scientist.Job Type &amp; LocationThis is a Contract to Hire position based out of Peachtree Corners, GA.Pay and BenefitsThe pay range for this position is $43.00 - $55.00/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)Workplace TypeThis is a fully onsite position in Peachtree Corners,GA.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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.

Scientist II - Reagent & Assay Development

Job Title: Scientist II, NMRJob DescriptionThe Scientist will support the Reference Standards Laboratory by performing NMR-based analytical testing and data interpretation to advance multiple ongoing projects. This role involves sample preparation, NMR data acquisition and analysis, documentation of experimental activities and reporting results, and collaboration with other team members to ensure project milestones are met.Responsibilities<ul><li>Perform NMR-based analytical testing and data interpretation to support ongoing laboratory projects.</li><li>Prepare and analyze samples, operate NMR instrumentation, and document and review results.</li><li>Maintain compliance with laboratory procedures and collaborate with team members to ensure timely completion of project deliverables.</li></ul>Essential Skills<ul><li>Hands-on NMR experience.</li><li>Strong analytical skills.</li><li>Ability to work independently in a fast-paced laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>B.A./B.S. in a scientific discipline with a minimum of 4 years of relevant laboratory experience, or M.S. degree in Chemistry, Pharmacy, or a related field with at least 2 years of relevant laboratory experience.</li><li>Prior hands-on experience with NMR instrumentation, data acquisition, and spectral interpretation is highly desirable.</li></ul>Work EnvironmentThis is an onsite laboratory environment with a high magnetic field. No pacemakers or implants are allowed. The environment requires the use of regular lab PPE, including gloves, lab coat, and safety goggles. Exposure to different levels of chemical hazard classification materials is expected, and it offers a highly collaborative team setting.Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $44.20 - $61.88/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)Workplace TypeThis is a fully onsite position in Rockville,MD.Application DeadlineThis position is anticipated to close on Sep 14, 2026.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.

Scientist II, NMR

Description
					The Scientist will support the Reference Standards Laboratory by performing NMR-based analytical testing and data interpretation to advance multiple ongoing projects. Responsibilities include sample preparation, NMR data acquisition and analysis, documentation of experimental activities and reporting results, and collaboration with other team members to ensure project milestones are met.
Summary of Duties:
• Perform NMR-based analytical testing and data interpretation to support ongoing laboratory projects; prepare and analyze samples, operate NMR instrumentation, document and review results, maintain compliance with laboratory procedures, and collaborate with team members to ensure timely completion of project deliverables.
										Skills
					NMR, analytical testing, data interpretation, data analysis, sample preparation, reporting, Chemistry, spectral interpretation
										Top Skills Details
					NMR,analytical testing,data interpretation,data analysis,sample preparation,reporting,Chemistry
										Additional Skills &amp; Qualifications
					Basic Qualifications:
• The position requires hands-on NMR experience, strong analytical skills, and the ability to work independently in a fast-paced laboratory environment.
• B.A./B.S. in a scientific discipline with a minimum of 4 years of relevant laboratory experience; or
• M.S. degree in Chemistry, Pharmacy, or a related field with at least 2 years of relevant laboratory experience.
• Prior hands-on experience with NMR instrumentation, data acquisition, and spectral interpretation is highly desirable to enable immediate contribution to ongoing laboratory projects.
										Experience Level
					Intermediate Level
					Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $44.20 - $61.88/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)Workplace TypeThis is a fully onsite position in Rockville,MD.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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: Scientist II, NMRJob DescriptionThe Scientist will support the Reference Standards Laboratory by performing NMR-based analytical testing and data interpretation to advance multiple ongoing projects. This role involves sample preparation, NMR data acquisition and analysis, documentation of experimental activities and reporting results, and collaboration with other team members to ensure project milestones are met.Responsibilities<ul><li>Perform NMR-based analytical testing and data interpretation to support ongoing laboratory projects.</li><li>Prepare and analyze samples, operate NMR instrumentation, and document and review results.</li><li>Maintain compliance with laboratory procedures and collaborate with team members to ensure timely completion of project deliverables.</li></ul>Essential Skills<ul><li>Hands-on NMR experience.</li><li>Strong analytical skills.</li><li>Ability to work independently in a fast-paced laboratory environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>B.A./B.S. in a scientific discipline with a minimum of 4 years of relevant laboratory experience, or M.S. degree in Chemistry, Pharmacy, or a related field with at least 2 years of relevant laboratory experience.</li><li>Prior hands-on experience with NMR instrumentation, data acquisition, and spectral interpretation is highly desirable.</li></ul>Work EnvironmentThis is an onsite laboratory environment with a high magnetic field. No pacemakers or implants are allowed. The environment requires the use of regular lab PPE, including gloves, lab coat, and safety goggles. Exposure to different levels of chemical hazard classification materials is expected, and it offers a highly collaborative team setting.Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $44.20 - $61.88/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)Workplace TypeThis is a fully onsite position in Rockville,MD.Application DeadlineThis position is anticipated to close on Sep 19, 2026.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.

<h1>Scientist III - Reagent &amp; Assay Development</h1>Location: Peachtree Corners, GA (On-Site)Pay Range: $57-$64/hr - based on experience<h2>Overview</h2>Seeking an experienced Scientist III to join a leading biotechnology organization focused on developing innovative immunohematology reagents and diagnostic assays. This role will play a key part in the development, optimization, and integration of diagnostic reagents and assays for automated in-vitro diagnostic platforms.The ideal candidate will bring strong expertise in assay development, immunology, immunohematology, transfusion medicine, or diagnostic product development and will thrive in a collaborative, fast-paced R&amp;D environment.<h2>Responsibilities</h2><ul><li>Independently design, plan, and execute complex laboratory experiments supporting reagent and assay development programs.</li><li>Develop, optimize, and characterize reagents, formulations, and assay parameters for automated diagnostic platforms.</li><li>Analyze scientific data, interpret results, and provide technical recommendations to project teams.</li><li>Evaluate assay performance, including sensitivity, specificity, precision, stability, reproducibility, interference, and robustness.</li><li>Lead experimental workstreams and Design of Experiments (DOE) activities within larger product development programs.</li><li>Troubleshoot technical issues related to reagent development, assay performance, platform integration, validation, and manufacturing transfer.</li><li>Support verification, validation, and commercialization efforts for new and existing diagnostic products.</li><li>Contribute to design documentation, technical reports, risk assessments, validation protocols, and regulatory submissions.</li><li>Collaborate with R&amp;D, Quality, Regulatory, Manufacturing, Systems Engineering, Software, and Technical Operations teams.</li><li>Mentor junior scientists and provide technical guidance to Scientist I and Scientist II team members.</li></ul><h2>Qualifications</h2><h3>Required</h3><ul><li>Bachelor's degree in Biology, Immunology, Biochemistry, Biomedical Sciences, or related scientific discipline with 7+ years of relevant experience.</li><li>OR Master's degree with 4+ years of relevant experience.</li><li>OR PhD with 1-2+ years of industry or post-doctoral experience.</li><li>Strong experience in reagent development, assay development, immunology, immunohematology, or transfusion medicine.</li><li>Experience independently planning and executing scientific research projects.</li><li>Proven ability to analyze complex scientific data and solve technical problems.</li><li>Excellent written and verbal communication skills.</li></ul><h3>Preferred</h3><ul><li>Experience developing assays or reagents for automated in-vitro diagnostic platforms.</li><li>Experience with immunohematology testing, serology, or blood banking technologies.</li><li>Familiarity with medical device, biotechnology, or diagnostic product development environments.</li><li>Experience leading Design of Experiments (DOE) studies.</li><li>Knowledge of product validation, manufacturing transfer, and regulatory requirements.</li></ul><h2>Why Join?</h2><ul><li>Opportunity to contribute to cutting-edge diagnostic technologies that impact patient care globally.</li><li>Collaborative environment with exposure to cross-functional product development teams.</li><li>Opportunity to lead technical projects and mentor junior scientists.</li><li>Comprehensive benefits including:<ul><li>Medical, Dental &amp; Vision Insurance</li><li>401(k) with Pre-Tax and Roth Contribution Options</li><li>Life Insurance</li><li>Short &amp; Long-Term Disability</li><li>Health Savings Account (HSA)</li><li>Transportation Benefits</li><li>Employee Assistance Program</li><li>PTO and Sick Leave Eligibility</li></ul></li></ul><h2>Ideal Backgrounds</h2><ul><li>Scientist III</li><li>Sr Scientist</li><li>Research Scientist</li><li>Sr Research Associate</li><li>Immunology Scientist</li><li>Immunohematology Scientist</li><li>Assay Development Scientist</li><li>Reagent Development Scientist</li><li>Diagnostic Development Scientist</li><li>Transfusion Medicine Scientist</li><li>Medical Device Scientist</li><li>Biotechnology Scientist</li></ul>Apply today to join an innovative team developing the next generation of immunohematology reagents and diagnostic assays for automated testing platforms.<h2></h2>lJob Type &amp; LocationThis is a Contract to Hire position based out of Peachtree Corners, GA.Pay and BenefitsThe pay range for this position is $57.00 - $64.00/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)Workplace TypeThis is a fully onsite position in Peachtree Corners,GA.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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.

Scientist III - Reagent & Assay Development

Description
					We are seeking a mid-career scientific professional (equivalent to USP Scientist III or higher) with expertise in biologics, microbiology, and compendial laboratory testing to serve as a subject matter expert responsible for translating, reviewing, and validating USP procedures for digital deployment.
The successful candidate will help transform complex laboratory procedures into structured, executable workflows while collaborating with scientific content, quality, informatics, and product teams to support vendor-neutral laboratory software environments.
Summary of Duties:
• Serve as scientific SME for USP General Chapters , , , and , interpreting compendial procedures for digital implementation.
• Create, review, and validate structured method content for scientific accuracy, procedural completeness, calculations, acceptance criteria, materials, equipment, and alignment with source documentation.
• Apply laboratory SOP and workflow expertise to ensure procedures reflect practical execution in regulated laboratory and manufacturing environments.
Perform scientific quality review, identify interpretation risks or discrepancies, and recommend improvements to content development and review processes.
• Collaborate with laboratory informatics and product teams to support workflow design, metadata capture, and implementation across LIMS, ELN, LES, and related systems.
• Support alignment with laboratory data standards, machine-readable content models, and structured data principles.
										Skills
					LIMS, ELN, LES, CDS, Biologics, Microbiology, compendial laboratory testing, digital implementation, validate method, USP General Chapters, SOP writing, controlled documentation, Microbiological testing, biologics development, cell based assays, protein characterization, sterile manufacturing environments, lab digitization, workflow automation, scientific content transformation, data standards, laboratory informatics, analytical datasets, AI, machine learning, scientific content management, knowledge extraction, Python, SQL, Power BI, Tableau, Allotrope Foundation, Pistoia Alliance
										Top Skills Details
					LIMS,ELN,LES,CDS,Biologics,Microbiology,compendial laboratory testing,digital implementation,validate method,USP General Chapters,SOP writing,controlled documentation
										Additional Skills &amp; Qualifications
					Basic Qualifications:
• Bachelor’s degree in Biology, Microbiology, Biochemistry, Biotechnology, Life Sciences, or a related scientific discipline; advanced degree preferred.
• 5+ years of experience in biologics, microbiology, compendial testing, analytical development, quality control, or regulated laboratory environments.
• Demonstrated expertise with USP General Chapters , , , and , including interpretation and application of compendial methods.
• 3+ years of experience authoring, reviewing, revising, or approving laboratory SOPs, test methods, work instructions, or related controlled documentation.
• Working knowledge of laboratory quality systems, data integrity requirements, laboratory workflows, and analytical instrumentation.
• Experience using laboratory information systems such as LIMS, ELN, LES, CDS, or similar platforms.
• Ability to translate laboratory procedures into structured, digitally executable workflows while maintaining scientific accuracy and compliance.
• Strong scientific writing, review, analytical, and cross-functional collaboration skills.

Preferred Qualifications:
• Advanced degree (MS or PhD) in Microbiology, Biotechnology, Biochemistry, Biological Sciences, or a related field.
• Experience in microbiological testing, biologics development, cell-based assays, protein characterization, or sterile manufacturing environments.
• Experience supporting laboratory digitization, workflow automation, or scientific content transformation initiatives.
• Development expertise with structured data formats, data standards, metadata management,
• FAIR data principles, or laboratory informatics frameworks.
• Experience applying data science, analytics, or data visualization techniques to laboratory, quality, or analytical datasets.
• Familiarity with AI and machine learning applications for scientific content management, laboratory operations, workflow automation, or knowledge extraction.
• Working knowledge of Python, SQL, Power BI,
										Experience Level
					Expert Level
					Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $52.11 - $74.25/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)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Sep 14, 2026.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.

Scientist III, Biologics SME

Job Title: Scientist III, Biologics Subject Matter ExpertJob DescriptionWe are seeking a mid-career scientific professional with expertise in biologics, microbiology, and compendial laboratory testing. This role involves serving as a subject matter expert responsible for translating, reviewing, and validating USP procedures for digital deployment. The successful candidate will transform complex laboratory procedures into structured, executable workflows and collaborate with scientific content, quality, informatics, and product teams to support vendor-neutral laboratory software environments.Responsibilities<ul><li>Serve as a scientific SME for USP General Chapters , , , and , interpreting compendial procedures for digital implementation.</li><li>Create, review, and validate structured method content for scientific accuracy, procedural completeness, calculations, acceptance criteria, materials, equipment, and alignment with source documentation.</li><li>Apply laboratory SOP and workflow expertise to ensure procedures reflect practical execution in regulated laboratory and manufacturing environments.</li><li>Perform scientific quality review, identify interpretation risks or discrepancies, and recommend improvements to content development and review processes.</li><li>Collaborate with laboratory informatics and product teams to support workflow design, metadata capture, and implementation across LIMS, ELN, LES, and related systems.</li><li>Support alignment with laboratory data standards, machine-readable content models, and structured data principles.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biology, Microbiology, Biochemistry, Biotechnology, Life Sciences, or a related scientific discipline; advanced degree preferred.</li><li>5+ years of experience in biologics, microbiology, compendial testing, analytical development, quality control, or regulated laboratory environments.</li><li>Demonstrated expertise with USP General Chapters , , , and , including interpretation and application of compendial methods.</li><li>3+ years of experience authoring, reviewing, revising, or approving laboratory SOPs, test methods, work instructions, or related controlled documentation.</li><li>Working knowledge of laboratory quality systems, data integrity requirements, laboratory workflows, and analytical instrumentation.</li><li>Experience using laboratory information systems such as LIMS, ELN, LES, CDS, or similar platforms.</li><li>Ability to translate laboratory procedures into structured, digitally executable workflows while maintaining scientific accuracy and compliance.</li><li>Strong scientific writing, review, analytical, and cross-functional collaboration skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree (MS or PhD) in Microbiology, Biotechnology, Biochemistry, Biological Sciences, or a related field.</li><li>Experience in microbiological testing, biologics development, cell-based assays, protein characterization, or sterile manufacturing environments.</li><li>Experience supporting laboratory digitization, workflow automation, or scientific content transformation initiatives.</li><li>Development expertise with structured data formats, data standards, metadata management.</li><li>Familiarity with FAIR data principles, laboratory informatics frameworks.</li><li>Experience applying data science, analytics, or data visualization techniques to laboratory, quality, or analytical datasets.</li><li>Familiarity with AI and machine learning applications for scientific content management, laboratory operations, workflow automation, or knowledge extraction.</li><li>Working knowledge of Python, SQL, Power BI.</li></ul>Work EnvironmentThe position offers remote working opportunities with a preference for candidates located in the DMV area. The role operates on East Coast hours, providing flexibility while ensuring collaboration with teams.Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $52.11 - $74.25/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)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Sep 25, 2026.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: Scientist III, Biologics Subject Matter ExpertJob DescriptionWe are seeking a mid-career scientific professional with expertise in biologics, microbiology, and compendial laboratory testing. This role involves serving as a subject matter expert responsible for translating, reviewing, and validating USP procedures for digital deployment. The successful candidate will transform complex laboratory procedures into structured, executable workflows and collaborate with scientific content, quality, informatics, and product teams to support vendor-neutral laboratory software environments.Responsibilities<ul><li>Serve as a scientific SME for USP General Chapters , , , and , interpreting compendial procedures for digital implementation.</li><li>Create, review, and validate structured method content for scientific accuracy, procedural completeness, calculations, acceptance criteria, materials, equipment, and alignment with source documentation.</li><li>Apply laboratory SOP and workflow expertise to ensure procedures reflect practical execution in regulated laboratory and manufacturing environments.</li><li>Perform scientific quality review, identify interpretation risks or discrepancies, and recommend improvements to content development and review processes.</li><li>Collaborate with laboratory informatics and product teams to support workflow design, metadata capture, and implementation across LIMS, ELN, LES, and related systems.</li><li>Support alignment with laboratory data standards, machine-readable content models, and structured data principles.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biology, Microbiology, Biochemistry, Biotechnology, Life Sciences, or a related scientific discipline; advanced degree preferred.</li><li>5+ years of experience in biologics, microbiology, compendial testing, analytical development, quality control, or regulated laboratory environments.</li><li>Demonstrated expertise with USP General Chapters , , , and , including interpretation and application of compendial methods.</li><li>3+ years of experience authoring, reviewing, revising, or approving laboratory SOPs, test methods, work instructions, or related controlled documentation.</li><li>Working knowledge of laboratory quality systems, data integrity requirements, laboratory workflows, and analytical instrumentation.</li><li>Experience using laboratory information systems such as LIMS, ELN, LES, CDS, or similar platforms.</li><li>Ability to translate laboratory procedures into structured, digitally executable workflows while maintaining scientific accuracy and compliance.</li><li>Strong scientific writing, review, analytical, and cross-functional collaboration skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree (MS or PhD) in Microbiology, Biotechnology, Biochemistry, Biological Sciences, or a related field.</li><li>Experience in microbiological testing, biologics development, cell-based assays, protein characterization, or sterile manufacturing environments.</li><li>Experience supporting laboratory digitization, workflow automation, or scientific content transformation initiatives.</li><li>Development expertise with structured data formats, data standards, metadata management.</li><li>Familiarity with FAIR data principles, laboratory informatics frameworks.</li><li>Experience applying data science, analytics, or data visualization techniques to laboratory, quality, or analytical datasets.</li><li>Familiarity with AI and machine learning applications for scientific content management, laboratory operations, workflow automation, or knowledge extraction.</li><li>Working knowledge of Python, SQL, Power BI.</li></ul>Work EnvironmentThe position offers remote working opportunities with a preference for candidates located in the DMV area. The role operates on East Coast hours, providing flexibility while ensuring collaboration with teams.Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $52.11 - $74.25/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)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Sep 19, 2026.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: Scientist III, Biologics Subject Matter ExpertJob DescriptionWe are seeking a mid-career scientific professional with expertise in biologics, microbiology, and compendial laboratory testing. This role involves serving as a subject matter expert responsible for translating, reviewing, and validating USP procedures for digital deployment. The successful candidate will transform complex laboratory procedures into structured, executable workflows and collaborate with scientific content, quality, informatics, and product teams to support vendor-neutral laboratory software environments.Responsibilities<ul><li>Serve as a scientific SME for USP General Chapters , , , and , interpreting compendial procedures for digital implementation.</li><li>Create, review, and validate structured method content for scientific accuracy, procedural completeness, calculations, acceptance criteria, materials, equipment, and alignment with source documentation.</li><li>Apply laboratory SOP and workflow expertise to ensure procedures reflect practical execution in regulated laboratory and manufacturing environments.</li><li>Perform scientific quality review, identify interpretation risks or discrepancies, and recommend improvements to content development and review processes.</li><li>Collaborate with laboratory informatics and product teams to support workflow design, metadata capture, and implementation across LIMS, ELN, LES, and related systems.</li><li>Support alignment with laboratory data standards, machine-readable content models, and structured data principles.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biology, Microbiology, Biochemistry, Biotechnology, Life Sciences, or a related scientific discipline; advanced degree preferred.</li><li>5+ years of experience in biologics, microbiology, compendial testing, analytical development, quality control, or regulated laboratory environments.</li><li>Demonstrated expertise with USP General Chapters , , , and , including interpretation and application of compendial methods.</li><li>3+ years of experience authoring, reviewing, revising, or approving laboratory SOPs, test methods, work instructions, or related controlled documentation.</li><li>Working knowledge of laboratory quality systems, data integrity requirements, laboratory workflows, and analytical instrumentation.</li><li>Experience using laboratory information systems such as LIMS, ELN, LES, CDS, or similar platforms.</li><li>Ability to translate laboratory procedures into structured, digitally executable workflows while maintaining scientific accuracy and compliance.</li><li>Strong scientific writing, review, analytical, and cross-functional collaboration skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Advanced degree (MS or PhD) in Microbiology, Biotechnology, Biochemistry, Biological Sciences, or a related field.</li><li>Experience in microbiological testing, biologics development, cell-based assays, protein characterization, or sterile manufacturing environments.</li><li>Experience supporting laboratory digitization, workflow automation, or scientific content transformation initiatives.</li><li>Development expertise with structured data formats, data standards, metadata management.</li><li>Familiarity with FAIR data principles, laboratory informatics frameworks.</li><li>Experience applying data science, analytics, or data visualization techniques to laboratory, quality, or analytical datasets.</li><li>Familiarity with AI and machine learning applications for scientific content management, laboratory operations, workflow automation, or knowledge extraction.</li><li>Working knowledge of Python, SQL, Power BI.</li></ul>Work EnvironmentThe position offers remote working opportunities with a preference for candidates located in the DMV area. The role operates on East Coast hours, providing flexibility while ensuring collaboration with teams.Job Type &amp; LocationThis is a Contract position based out of Rockville, MD.Pay and BenefitsThe pay range for this position is $52.11 - $74.25/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)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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.

Scientist – Cell-Based Assay Development (In Vitro Services)We are seeking an experienced scientist to lead the development, optimization, and execution of cell-based assays supporting client research and testing programs. This is a scientifically rigorous, client-facing role that combines hands-on assay development with study leadership and regulatory compliance within a GLP/cGMP-regulated CRO environment.This position is ideal for a motivated scientist with a strong cell biology or immunology background who thrives in a fast-paced, collaborative setting and is ready to take ownership of complex in vitro programs from inception through final reporting.Key Responsibilities<ul><li>Design, develop, optimize, validate, and implement in vitro and cell-based assays to support diverse client projects across therapeutic and research programs</li><li>Work with a broad range of cellular models, including primary cells, immortalized cell lines, and transfected or overexpressing systems</li><li>Apply expertise across a wide range of techniques, including cell culture, transfection, gene and protein expression analysis, pathway characterization, ELISA, ELISpot, cytokine analysis, and immunological assays</li><li>Lead studies as Study Director (GLP) or Lead Analyst (cGMP), serving as the primary scientific point of contact from project scoping and proposal development through data analysis and final report delivery</li><li>Provide scientific, experimental, and regulatory guidance to both clients and internal cross-functional teams</li><li>Identify opportunities to develop new testing capabilities and support the expansion of the organization's in vitro service offerings</li><li>Ensure full compliance with GLP/cGMP requirements, laboratory SOPs, and applicable regulatory standards</li><li>Maintain thorough, accurate scientific documentation in accordance with good documentation practices</li><li>Collaborate effectively across departments while maintaining clear written and verbal communication with internal and external stakeholders</li></ul>QualificationsRequired:<ul><li>M.S. or Ph.D. in Biology, Cell Biology, Molecular Biology, Immunology, or a closely related field (B.S. candidates with substantial industry experience will be considered)</li><li>Strong hands-on experience with cell culture, cellular assay development, molecular biology techniques, and immunological assays</li><li>Demonstrated ability to work independently, manage competing priorities, and troubleshoot complex scientific challenges</li><li>Excellent communication, documentation, and problem-solving skills</li><li>Willingness to work flexible hours and safely handle hazardous laboratory materials as required</li></ul>Preferred:<ul><li>Experience in a regulated GLP and/or cGMP laboratory environment</li><li>BSL-2 laboratory operations experience</li><li>Functional assay development experience (receptor activation, signaling pathways, cell viability, potency assays, etc.)</li><li>Prior experience as a GLP Study Director or Lead Analyst in a CRO setting</li><li>Familiarity with regulatory submissions or dossier support (IND, BLA, 510(k), etc.)</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Hercules, CA.Pay and BenefitsThe pay range for this position is $40.86 - $48.07/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)Workplace TypeThis is a fully onsite position in Hercules,CA.Application DeadlineThis position is anticipated to close on Sep 17, 2026.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.

Scientist, In Vitro

Scrum MasterJob DescriptionThis Scrum Master role focuses on facilitating agile ceremonies for individual hardware and robotics subsystem teams, ensuring smooth collaboration across cross-functional groups and protecting the Product Owner’s time for strategic work such as requirements, stakeholder engagement, and roadmap planning.Responsibilities<ul><li>Facilitate core Scrum ceremonies for hardware and robotics subsystem teams, including sprint planning, daily standups, sprint reviews, and retrospectives.</li><li>Plan and manage all ceremony logistics, including scheduling meetings, defining agendas, and setting up tooling to support effective collaboration.</li><li>Protect the Product Owner’s time by handling ceremony and planning logistics, enabling the Product Owner to focus on requirements, stakeholders, and roadmap activities.</li><li>Coordinate and support multiple interconnected subsystem teams working on robotics, sensors, controls, software applications, and remote support infrastructure.</li><li>Promote agile best practices within hardware development teams and encourage continuous improvement in team processes and communication.</li><li>Collaborate effectively with cross-functional teams to remove impediments, improve workflows, and ensure alignment across disciplines.</li><li>Use Jira and other agile tools to organize work, track progress, and maintain transparency on team commitments and delivery.</li></ul>Essential Skills<ul><li>At least 3+ years of experience facilitating Scrum and agile ceremonies for hardware development teams.</li><li>Hardware development experience </li><li>Hands-on experience with Jira for agile planning, tracking, and reporting.</li><li>Certified Scrum Master (CSM) or Professional Scrum Master I (PSM I).</li><li>Experience working with robotics projects or robotics-related systems.</li><li>Ability to work effectively with cross-functional teams across disciplines such as robotics, sensors, controls, software, and support.</li><li>Strong organizational and communication skills to manage ceremony logistics and support team collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience applying agile practices in complex, multi-subsystem environments.</li><li>Familiarity with sensors, controls, software applications, and remote support infrastructure in a robotics context.</li><li>Demonstrated ability to foster a culture of continuous improvement and teamwork.</li><li>Comfort facilitating meetings and guiding discussions to keep teams focused and productive.</li></ul>Work EnvironmentThis is a fully onsite role in a growing company that builds a Titan robotic construction printer composed of multiple interconnected subsystems, including robotics, sensors, controls, software applications, and remote support infrastructure. You will work closely with hardware and robotics teams in a collaborative environment where agile practices are central to daily operations. The company offers 10 paid holidays and 1 week of PTO, ideally used during a holiday shutdown in December, and provides opportunities for upward mobility and professional growth.Job Type &amp; LocationThis is a Contract to Hire position based out of Austin, TX.Pay and BenefitsThe pay range for this position is $70.00 - $80.00/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)Workplace TypeThis is a fully onsite position in Austin,TX.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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.

Scrum Master

I'm currently hiring for Scrum Master in Austin, TX! Job DescriptionThis Scrum Master role focuses on facilitating agile ceremonies for individual hardware and robotics subsystem teams, ensuring smooth collaboration across cross-functional groups and protecting the Product Owner’s time for strategic work such as requirements, stakeholder engagement, and roadmap planning.Responsibilities<ul><li>Facilitate core Scrum ceremonies for hardware and robotics subsystem teams, including sprint planning, daily standups, sprint reviews, and retrospectives.</li><li>Plan and manage all ceremony logistics, including scheduling meetings, defining agendas, and setting up tooling to support effective collaboration.</li><li>Protect the Product Owner’s time by handling ceremony and planning logistics, enabling the Product Owner to focus on requirements, stakeholders, and roadmap activities.</li><li>Coordinate and support multiple interconnected subsystem teams working on robotics, sensors, controls, software applications, and remote support infrastructure.</li><li>Promote agile best practices within hardware development teams and encourage continuous improvement in team processes and communication.</li><li>Collaborate effectively with cross-functional teams to remove impediments, improve workflows, and ensure alignment across disciplines.</li><li>Use Jira and other agile tools to organize work, track progress, and maintain transparency on team commitments and delivery.</li></ul>Essential Skills<ul><li>At least 3+ years of experience facilitating Scrum and agile ceremonies for hardware development teams.</li><li>Hardware development experience</li><li>Hands-on experience with Jira for agile planning, tracking, and reporting.</li><li>Certified Scrum Master (CSM) or Professional Scrum Master I (PSM I).</li><li>Experience working with robotics projects or robotics-related systems.</li><li>Ability to work effectively with cross-functional teams across disciplines such as robotics, sensors, controls, software, and support.</li><li>Strong organizational and communication skills to manage ceremony logistics and support team collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience applying agile practices in complex, multi-subsystem environments.</li><li>Familiarity with sensors, controls, software applications, and remote support infrastructure in a robotics context.</li><li>Demonstrated ability to foster a culture of continuous improvement and teamwork.</li><li>Comfort facilitating meetings and guiding discussions to keep teams focused and productive.</li></ul>Work EnvironmentThis is a fully onsite role in a growing company that builds a Titan robotic construction printer composed of multiple interconnected subsystems, including robotics, sensors, controls, software applications, and remote support infrastructure. You will work closely with hardware and robotics teams in a collaborative environment where agile practices are central to daily operations. The company offers 10 paid holidays and 1 week of PTO, ideally used during a holiday shutdown in December, and provides opportunities for upward mobility and professional growth.Job Type &amp; LocationThis is a Permanent position based out of Austin, TX.Pay and BenefitsThe pay range for this position is $70.00 - $80.00/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)Workplace TypeThis is a fully onsite position in Austin,TX.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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: Scrum MasterJob DescriptionAs a Scrum Master, you will serve as a facilitator for ART level events and processes, including Value Stream Mapping, Roadmap creation, Backlog management, and Program Increment (PI) Planning. You will work as an Agile coach with mission owners, stakeholders, Product Owners, Scrum Masters, and team members to ensure alignment with Agile/DevSecOps principles. Your role will involve establishing and tracking key ART level metrics and improving the flow of value through Value Streams.Responsibilities<ul><li>Facilitate ART level events such as Product Owner Sync, Scrum of Scrums, PI Review, Demonstrations, Retrospectives, and Inspect and Adapt Workshops.</li><li>Establish and track key ART level metrics and communicate them to program and technical leadership.</li><li>Improve and assess DevSecOps and Release on Demand practices in the Continuous Delivery Pipeline.</li><li>Facilitate Regular System Demos to ensure objectives are met and present features to stakeholders.</li><li>Assess the Agility level of the ART and drive relentless improvement through training and skills path guidance.</li></ul>Essential Skills<ul><li>3+ years of related experience with a Bachelor's degree.</li><li>Secret Clearance.</li><li>Industry recognized Agile certification (Scaled Agile, Scrum.org, Scrum, Inc., Scrum Alliance, or PMI).</li><li>Demonstrated Program/Project Management and leadership skills.</li><li>Ability to lead multi-functional teams and coordinate work with common goals.</li></ul>Additional Skills &amp; Qualifications<ul><li>Comfortable imparting knowledge and guiding leaders and Agile teams on scaling principles.</li><li>Experience driving continuous improvement across diverse stakeholder groups.</li><li>Experience with Atlassian tools (Jira, Confluence, etc.).</li></ul>Work EnvironmentThis position offers a hybrid work environment, allowing for a combination of remote and in-office work.We reserve the right to pay above or below the posted wage based on factors unrelated to sex, race, or any other protected classification.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. This temporary role may be eligible for the following:<ul><li>Medical, Dental &amp; Vision</li><li>401(k)/Roth</li><li>Basic/Supplemental Life &amp; AD&amp;D</li><li>Short and long-term disability</li><li>HSA &amp; DCFSA</li><li>Transportation benefits</li><li>Employee Assistance Program</li><li>Company Paid Time off or State Sick Leave</li></ul>Job Type &amp; LocationThis is a Contract position based out of Colorado Springs, CO.Pay and BenefitsThe pay range for this position is $40.00 - $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)Workplace TypeThis is a hybrid position in Colorado Springs,CO.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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: Scrum MasterJob DescriptionAs a Scrum Master, you will serve as a facilitator for ART level events and processes, including Value Stream Mapping, Roadmap creation, Backlog management, and Program Increment (PI) Planning. You will work as an Agile coach with mission owners, stakeholders, Product Owners, Scrum Masters, and team members to ensure alignment with Agile/DevSecOps principles. Your role will involve establishing and tracking key ART level metrics and improving the flow of value through Value Streams.Responsibilities<ul><li>Facilitate ART level events such as Product Owner Sync, Scrum of Scrums, PI Review, Demonstrations, Retrospectives, and Inspect and Adapt Workshops.</li><li>Establish and track key ART level metrics and communicate them to program and technical leadership.</li><li>Improve and assess DevSecOps and Release on Demand practices in the Continuous Delivery Pipeline.</li><li>Facilitate Regular System Demos to ensure objectives are met and present features to stakeholders.</li><li>Assess the Agility level of the ART and drive relentless improvement through training and skills path guidance.</li></ul>Essential Skills<ul><li>3+ years of related experience with a Bachelor's degree.</li><li>Secret Clearance.</li><li>Industry recognized Agile certification (Scaled Agile, Scrum.org, Scrum, Inc., Scrum Alliance, or PMI).</li><li>Demonstrated Program/Project Management and leadership skills.</li><li>Ability to lead multi-functional teams and coordinate work with common goals.</li></ul>Additional Skills &amp; Qualifications<ul><li>Comfortable imparting knowledge and guiding leaders and Agile teams on scaling principles.</li><li>Experience driving continuous improvement across diverse stakeholder groups.</li><li>Experience with Atlassian tools (Jira, Confluence, etc.).</li></ul>Work EnvironmentThis position offers a hybrid work environment, allowing for a combination of remote and in-office work.Job Type &amp; LocationThis is a Contract position based out of Colorado Springs, CO.Pay and BenefitsThe pay range for this position is $40.00 - $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)Workplace TypeThis is a hybrid position in Colorado Springs,CO.Application DeadlineThis position is anticipated to close on Sep 22, 2026.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.

Scrum MasterJob DescriptionThis Scrum Master role focuses on facilitating agile ceremonies for individual hardware and robotics subsystem teams, ensuring smooth collaboration across cross-functional groups and protecting the Product Owner’s time for strategic work such as requirements, stakeholder engagement, and roadmap planning.Responsibilities<ul><li>Facilitate core Scrum ceremonies for hardware and robotics subsystem teams, including sprint planning, daily standups, sprint reviews, and retrospectives.</li><li>Plan and manage all ceremony logistics, including scheduling meetings, defining agendas, and setting up tooling to support effective collaboration.</li><li>Protect the Product Owner’s time by handling ceremony and planning logistics, enabling the Product Owner to focus on requirements, stakeholders, and roadmap activities.</li><li>Coordinate and support multiple interconnected subsystem teams working on robotics, sensors, controls, software applications, and remote support infrastructure.</li><li>Promote agile best practices within hardware development teams and encourage continuous improvement in team processes and communication.</li><li>Collaborate effectively with cross-functional teams to remove impediments, improve workflows, and ensure alignment across disciplines.</li><li>Use Jira and other agile tools to organize work, track progress, and maintain transparency on team commitments and delivery.</li></ul>Essential Skills<ul><li>At least 3+ years of experience facilitating Scrum and agile ceremonies for hardware development teams.</li><li>Hardware development experience </li><li>Hands-on experience with Jira for agile planning, tracking, and reporting.</li><li>Certified Scrum Master (CSM) or Professional Scrum Master I (PSM I).</li><li>Experience working with robotics projects or robotics-related systems.</li><li>Ability to work effectively with cross-functional teams across disciplines such as robotics, sensors, controls, software, and support.</li><li>Strong organizational and communication skills to manage ceremony logistics and support team collaboration.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience applying agile practices in complex, multi-subsystem environments.</li><li>Familiarity with sensors, controls, software applications, and remote support infrastructure in a robotics context.</li><li>Demonstrated ability to foster a culture of continuous improvement and teamwork.</li><li>Comfort facilitating meetings and guiding discussions to keep teams focused and productive.</li></ul>Work EnvironmentThis is a fully onsite role in a growing company that builds a Titan robotic construction printer composed of multiple interconnected subsystems, including robotics, sensors, controls, software applications, and remote support infrastructure. You will work closely with hardware and robotics teams in a collaborative environment where agile practices are central to daily operations. The company offers 10 paid holidays and 1 week of PTO, ideally used during a holiday shutdown in December, and provides opportunities for upward mobility and professional growth.Job Type &amp; LocationThis is a Contract to Hire position based out of Austin, Texas.Pay and BenefitsThe pay range for this position is $70.00 - $80.00/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)Workplace TypeThis is a fully onsite position in Austin,Texas.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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: Software Development Engineer in Test (SDET)Job DescriptionThis role blends hands-on software development with a strong focus on quality engineering and automated testing for mobile applications. You will contribute to both functional and non-functional testing, ensuring that features meet acceptance criteria and user story requirements while building scalable automation solutions around the Flutter platform and related mobile technologies.Responsibilities<ul><li>Design, develop, and maintain robust automated test frameworks for UI, API, and integration testing across mobile applications.</li><li>Build scalable and reusable test automation solutions around the Flutter platform to support multiple product teams.</li><li>Integrate automated tests into CI/CD YAML pipelines using a test automation platform built on Azure DevOps.</li><li>Partner with the test automation platform team to enhance and extend the platform capabilities used by many product teams.</li><li>Collaborate with developers, verification engineers, and product owners to define test strategies, acceptance criteria, and quality goals.</li><li>Perform functional, regression, smoke, performance, and reliability testing to ensure high-quality releases.</li><li>Implement shift-left testing practices to embed quality early in the software development lifecycle.</li><li>Participate in design and code reviews to ensure testability, reliability, and adherence to quality standards.</li><li>Work closely with DevOps, the test automation platform team, and developers to improve release pipelines and automate reliability checks.</li><li>Partner with the development team to contribute to feature and functionality development where needed.</li><li>Design meaningful, deterministic tests aligned with requirements and risk controls.</li><li>Maintain and improve automated tests over time, focusing on reliability, stability, and ease of maintenance.</li></ul>Essential Skills<ul><li>Minimum 4 years of hands-on mobile app development experience in Flutter and/or iOS and/or Android (Kotlin), contributing directly to production codebases.</li><li>At least 4 years of experience designing and implementing automated tests for mobile applications, including unit, UI/widget, and integration tests, with ongoing test maintenance and reliability improvements.</li><li>Strong understanding of mobile architecture, state management, and data flow, with the ability to apply this knowledge to improve testability and reliability.</li><li>Ability to read, reason about, and contribute to production code, and provide constructive code review feedback.</li><li>Proficiency in designing meaningful, deterministic tests that align with functional requirements and risk controls.</li><li>Skilled in unit, widget/UI, integration, and end-to-end testing approaches for mobile applications.</li><li>Experience building reliable mobile automation, such as Flutter integration tests, simulators/mocks, and API automation.</li><li>Experience working with agile development methodologies and project management tools such as JIRA, Azure DevOps, and Agile/Scrum practices.</li><li> automation and SDET practices, with hands-on experience in Kotlin, iOS, or embedded systems as relevant to mobile testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of industry standards and regulations, such as IEC-related standards.</li><li>Experience with Bluetooth Low Energy (BLE) interaction testing, including pairing, reconnect behavior, retries, error states, and diagnosing failure modes across mobile, embedded devices, and cloud boundaries.</li><li>Familiarity with structured verification workflows and tooling, including test management and traceability systems.</li><li>Experience in regulated environments, such as medical devices or Software as a Medical Device (SaMD), particularly regulated mobile applications.</li><li>Strong collaboration and communication skills to work effectively with cross-functional engineering and product teams.</li><li>Attention to detail and a passion for building reliable, maintainable test automation solutions.</li></ul>Work EnvironmentYou will work in a modern, engineering-focused environment that emphasizes automation, reliability, and continuous improvement. The team uses Azure DevOps-based CI/CD pipelines, agile methodologies, and project management tools such as JIRA and ADO. You will collaborate closely with developers, verification engineers, DevOps specialists, and product owners, participating in design and code reviews and contributing to both feature development and test strategy. The environment supports structured verification workflows, test management, and traceability systems, particularly for mobile and potentially embedded or regulated products. Work focuses on mobile technologies including Flutter, iOS, Android (Kotlin), BLE interactions, and integration with cloud and embedded systems, with a strong emphasis on quality engineering and robust automated testingJob Type &amp; LocationThis is a Contract position based out of Golden Valley, MN.Pay and BenefitsThe pay range for this position is $50.00 - $80.00/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)Workplace TypeThis is a hybrid position in Golden Valley,MN.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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.

Sdet Software Developer In Test

Job Title: Software Development Engineer in Test (SDET)Job DescriptionThis role blends hands-on software development with a strong focus on quality engineering and automated testing for mobile applications. You will contribute to both functional and non-functional testing, ensuring that features meet acceptance criteria and user story requirements while building scalable automation solutions around the Flutter platform and related mobile technologies.Responsibilities<ul><li>Design, develop, and maintain robust automated test frameworks for UI, API, and integration testing across mobile applications.</li><li>Build scalable and reusable test automation solutions around the Flutter platform to support multiple product teams.</li><li>Integrate automated tests into CI/CD YAML pipelines using a test automation platform built on Azure DevOps.</li><li>Partner with the test automation platform team to enhance and extend the platform capabilities used by many product teams.</li><li>Collaborate with developers, verification engineers, and product owners to define test strategies, acceptance criteria, and quality goals.</li><li>Perform functional, regression, smoke, performance, and reliability testing to ensure high-quality releases.</li><li>Implement shift-left testing practices to embed quality early in the software development lifecycle.</li><li>Participate in design and code reviews to ensure testability, reliability, and adherence to quality standards.</li><li>Work closely with DevOps, the test automation platform team, and developers to improve release pipelines and automate reliability checks.</li><li>Partner with the development team to contribute to feature and functionality development where needed.</li><li>Design meaningful, deterministic tests aligned with requirements and risk controls.</li><li>Maintain and improve automated tests over time, focusing on reliability, stability, and ease of maintenance.</li></ul>Essential Skills<ul><li>Minimum 4 years of hands-on mobile app development experience in Flutter and/or iOS and/or Android (Kotlin), contributing directly to production codebases.</li><li>At least 4 years of experience designing and implementing automated tests for mobile applications, including unit, UI/widget, and integration tests, with ongoing test maintenance and reliability improvements.</li><li>Strong understanding of mobile architecture, state management, and data flow, with the ability to apply this knowledge to improve testability and reliability.</li><li>Ability to read, reason about, and contribute to production code, and provide constructive code review feedback.</li><li>Proficiency in designing meaningful, deterministic tests that align with functional requirements and risk controls.</li><li>Skilled in unit, widget/UI, integration, and end-to-end testing approaches for mobile applications.</li><li>Experience building reliable mobile automation, such as Flutter integration tests, simulators/mocks, and API automation.</li><li>Experience working with agile development methodologies and project management tools such as JIRA, Azure DevOps, and Agile/Scrum practices.</li><li> automation and SDET practices, with hands-on experience in Kotlin, iOS, or embedded systems as relevant to mobile testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of industry standards and regulations, such as IEC-related standards.</li><li>Experience with Bluetooth Low Energy (BLE) interaction testing, including pairing, reconnect behavior, retries, error states, and diagnosing failure modes across mobile, embedded devices, and cloud boundaries.</li><li>Familiarity with structured verification workflows and tooling, including test management and traceability systems.</li><li>Experience in regulated environments, such as medical devices or Software as a Medical Device (SaMD), particularly regulated mobile applications.</li><li>Strong collaboration and communication skills to work effectively with cross-functional engineering and product teams.</li><li>Attention to detail and a passion for building reliable, maintainable test automation solutions.</li></ul>Work EnvironmentYou will work in a modern, engineering-focused environment that emphasizes automation, reliability, and continuous improvement. The team uses Azure DevOps-based CI/CD pipelines, agile methodologies, and project management tools such as JIRA and ADO. You will collaborate closely with developers, verification engineers, DevOps specialists, and product owners, participating in design and code reviews and contributing to both feature development and test strategy. The environment supports structured verification workflows, test management, and traceability systems, particularly for mobile and potentially embedded or regulated products. Work focuses on mobile technologies including Flutter, iOS, Android (Kotlin), BLE interactions, and integration with cloud and embedded systems, with a strong emphasis on quality engineering and robust automated testingJob Type &amp; LocationThis is a Contract position based out of Golden Valley, MN.Pay and BenefitsThe pay range for this position is $50.00 - $80.00/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)Workplace TypeThis is a hybrid position in Golden Valley,MN.Application DeadlineThis position is anticipated to close on Sep 17, 2026.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: Software Development Engineer in Test (SDET)Job DescriptionThis role blends hands-on software development with a strong focus on quality engineering and automated testing for mobile applications. You will contribute to both functional and non-functional testing, ensuring that features meet acceptance criteria and user story requirements while building scalable automation solutions around the Flutter platform and related mobile technologies.Responsibilities<ul><li>Design, develop, and maintain robust automated test frameworks for UI, API, and integration testing across mobile applications.</li><li>Build scalable and reusable test automation solutions around the Flutter platform to support multiple product teams.</li><li>Integrate automated tests into CI/CD YAML pipelines using a test automation platform built on Azure DevOps.</li><li>Partner with the test automation platform team to enhance and extend the platform capabilities used by many product teams.</li><li>Collaborate with developers, verification engineers, and product owners to define test strategies, acceptance criteria, and quality goals.</li><li>Perform functional, regression, smoke, performance, and reliability testing to ensure high-quality releases.</li><li>Implement shift-left testing practices to embed quality early in the software development lifecycle.</li><li>Participate in design and code reviews to ensure testability, reliability, and adherence to quality standards.</li><li>Work closely with DevOps, the test automation platform team, and developers to improve release pipelines and automate reliability checks.</li><li>Partner with the development team to contribute to feature and functionality development where needed.</li><li>Design meaningful, deterministic tests aligned with requirements and risk controls.</li><li>Maintain and improve automated tests over time, focusing on reliability, stability, and ease of maintenance.</li></ul>Essential Skills<ul><li>Minimum 4 years of hands-on mobile app development experience in Flutter and/or iOS and/or Android (Kotlin), contributing directly to production codebases.</li><li>At least 4 years of experience designing and implementing automated tests for mobile applications, including unit, UI/widget, and integration tests, with ongoing test maintenance and reliability improvements.</li><li>Strong understanding of mobile architecture, state management, and data flow, with the ability to apply this knowledge to improve testability and reliability.</li><li>Ability to read, reason about, and contribute to production code, and provide constructive code review feedback.</li><li>Proficiency in designing meaningful, deterministic tests that align with functional requirements and risk controls.</li><li>Skilled in unit, widget/UI, integration, and end-to-end testing approaches for mobile applications.</li><li>Experience building reliable mobile automation, such as Flutter integration tests, simulators/mocks, and API automation.</li><li>Experience working with agile development methodologies and project management tools such as JIRA, Azure DevOps, and Agile/Scrum practices.</li><li> automation and SDET practices, with hands-on experience in Kotlin, iOS, or embedded systems as relevant to mobile testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of industry standards and regulations, such as IEC-related standards.</li><li>Experience with Bluetooth Low Energy (BLE) interaction testing, including pairing, reconnect behavior, retries, error states, and diagnosing failure modes across mobile, embedded devices, and cloud boundaries.</li><li>Familiarity with structured verification workflows and tooling, including test management and traceability systems.</li><li>Experience in regulated environments, such as medical devices or Software as a Medical Device (SaMD), particularly regulated mobile applications.</li><li>Strong collaboration and communication skills to work effectively with cross-functional engineering and product teams.</li><li>Attention to detail and a passion for building reliable, maintainable test automation solutions.</li></ul>Work EnvironmentYou will work in a modern, engineering-focused environment that emphasizes automation, reliability, and continuous improvement. The team uses Azure DevOps-based CI/CD pipelines, agile methodologies, and project management tools such as JIRA and ADO. You will collaborate closely with developers, verification engineers, DevOps specialists, and product owners, participating in design and code reviews and contributing to both feature development and test strategy. The environment supports structured verification workflows, test management, and traceability systems, particularly for mobile and potentially embedded or regulated products. Work focuses on mobile technologies including Flutter, iOS, Android (Kotlin), BLE interactions, and integration with cloud and embedded systems, with a strong emphasis on quality engineering and robust automated testingJob Type &amp; LocationThis is a Permanent position based out of Golden Valley, MN.Pay and BenefitsThe pay range for this position is $50.00 - $80.00/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)Workplace TypeThis is a hybrid position in Golden Valley,MN.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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: Seasonal Soy Bean Production SpecialistJob DescriptionThe Seasonal Soy Bean Production Specialist plays a crucial role at a seed production facility during the peak harvest and seed processing season. This position involves operating and monitoring seed cleaning, treatment, packaging, and shipping processes while ensuring compliance with safety, quality, and operational standards. The role requires flexibility to support a 24-hour production schedule, including day, evening, overnight, weekend, and overtime shifts as needed.Responsibilities<ul><li>Operate and monitor seed cleaning, treatment, and packaging equipment using plant software systems.</li><li>Support daily seed processing activities to achieve production and throughput goals.</li><li>Perform routine equipment inspections, troubleshooting, and preventive maintenance activities.</li><li>Collect and document quality assurance and quality control (QA/QC) data.</li><li>Follow all Standard Operating Procedures (SOPs), safety protocols, and regulatory requirements.</li><li>Assist with material handling, seed receiving, storage, shipping, and packaging activities.</li><li>Work collaboratively with production team members and site leadership to maintain efficient operations.</li><li>Maintain accurate production records and documentation.</li><li>Perform general warehouse duties as assigned.</li></ul>Essential Skills<ul><li>High school diploma or GED.</li><li>Ability to work in a fast-paced production environment.</li><li>Basic computer skills.</li><li>Strong attention to detail and commitment to safety.</li><li>Ability to communicate effectively and work as part of a team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree, technical certification, or vocational training is preferred.</li><li>1-2 years of manufacturing, warehouse, agricultural, or production experience is preferred.</li><li>Experience with SAP or other production tracking systems is preferred.</li><li>Experience documenting production or quality data is preferred.</li></ul>Work EnvironmentThe facility operates in ambient warehouse conditions and is not climate controlled. Personal Protective Equipment (PPE) is required, including safety glasses. Additional PPE, such as hearing protection or respiratory protection, may be required based on specific work assignments. Long pants and sleeves may be required in designated work areas. The role involves working in an active warehouse environment, with the ability to lift, push, pull, and carry up to 65 pounds, and perform repetitive tasks throughout the shift. The facility operates on a 24-hour production schedule during peak season, with day, evening, and overnight shifts, as well as potential overtime, weekend, and holiday work.Job Type &amp; LocationThis is a Contract position based out of Centralia, 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)Workplace TypeThis is a fully onsite position in Centralia,IL.Application DeadlineThis position is anticipated to close on Sep 25, 2026.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.

Seasonal Soy Bean Production Specialist

Job Title: Seasonal Soy Bean Production SpecialistJob DescriptionThe Seasonal Soy Bean Production Specialist supports a high-volume seed production facility during peak harvest and seed processing season. In this hands-on role, you operate and monitor seed cleaning, treatment, packaging, and shipping processes while maintaining strict safety, quality, and operational standards. You work within a warehouse environment and provide flexible support to a 24-hour production schedule, including day, evening, overnight, weekend, and overtime shifts as business needs require.Responsibilities<ul><li>Operate and monitor seed cleaning, treatment, and packaging equipment using plant software systems.</li><li>Support daily seed processing activities to achieve production, throughput, and quality goals.</li><li>Perform routine equipment inspections, basic troubleshooting, and preventive maintenance activities to maintain reliable operations.</li><li>Collect, record, and document quality assurance and quality control (QA/QC) data in accordance with established procedures.</li><li>Follow all Standard Operating Procedures (SOPs), safety protocols, and applicable regulatory requirements at all times.</li><li>Assist with material handling, including seed receiving, storage, shipping, and packaging activities.</li><li>Work collaboratively with production team members and site leadership to maintain efficient and safe operations.</li><li>Maintain accurate production records and documentation for processing, inventory, and quality activities.</li><li>Perform general warehouse duties as assigned, including cleaning, organizing, and supporting overall facility readiness.</li></ul>Essential Skills<ul><li>High school diploma or GED.</li><li>Ability to work effectively in a fast-paced production and warehouse environment.</li><li>Basic computer skills to operate plant software systems and enter production or quality data.</li><li>Strong attention to detail with a consistent focus on safety and quality standards.</li><li>Ability to communicate clearly and work cooperatively as part of a team.</li><li>Ability to lift, push, pull, and carry up to 65 pounds.</li><li>Ability to stand, walk, bend, and perform repetitive tasks throughout the shift.</li><li>Ability to work safely and productively in an active warehouse environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree, technical certification, or vocational training in a relevant field.</li><li>1–2 years of experience in manufacturing, warehouse, agricultural, or production environments.</li><li>Interest in agriculture, biology, seed quality, or laboratory-related work.</li><li>Experience with SAP or other production tracking or enterprise resource planning systems.</li><li>Experience documenting production or quality data in compliance with established procedures.</li><li>Demonstrated ability to support quality control activities and follow QA/QC processes.</li></ul>Work EnvironmentThis role is based in an active warehouse and seed production facility with ambient conditions; the facility is not climate controlled, so temperatures may vary with the seasons. Personal Protective Equipment (PPE), including safety glasses, is required, and additional PPE such as hearing protection or respiratory protection may be needed depending on specific tasks. Long pants and sleeves may be required in designated work areas. The position supports a seasonal assignment aligned with harvest and seed processing operations. During peak season, the facility operates on a 24-hour production schedule, and you must be available for day, evening, and overnight shifts, as well as overtime, weekend, and holiday work as needed. Work schedules may change during the season based on operational needs, and initial assignments may start on a single shift before transitioning to multi-shift operations in October. The environment offers the opportunity to support a critical agricultural operation processing more than 3 million seed units annually, gain valuable manufacturing and warehouse experience, and contribute to food and agriculture innovation in a team-oriented setting.Job Type &amp; LocationThis is a Contract position based out of Centralia, 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)Workplace TypeThis is a fully onsite position in Centralia,IL.Application DeadlineThis position is anticipated to close on Sep 6, 2026.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.

<h2 style="text-align:center;">Seasonal Soy Bean Production Specialist</h2>Job DescriptionThe Seasonal Soy Bean Production Specialist supports a high-volume seed production facility during peak harvest and seed processing season. You operate and monitor seed cleaning, treatment, packaging, and shipping processes while maintaining strict safety, quality, and operational standards. This is a hands-on production role in a warehouse environment that requires flexibility to work across a 24-hour production schedule, including day, evening, overnight, weekend, and overtime shifts as business needs evolve.Responsibilities<ul><li>Operate and monitor seed cleaning, treatment, and packaging equipment using plant software systems.</li><li>Support daily seed processing activities to meet production, quality, and throughput goals.</li><li>Perform routine equipment inspections and basic troubleshooting to identify issues and minimize downtime.</li><li>Carry out preventive maintenance activities in accordance with established procedures.</li><li>Collect, record, and verify quality assurance and quality control (QA/QC) data for seed processing operations.</li><li>Follow all Standard Operating Procedures (SOPs), safety protocols, and applicable regulatory requirements.</li><li>Assist with material handling activities, including seed receiving, storage, shipping, and packaging.</li><li>Work collaboratively with production team members and site leadership to maintain efficient and safe operations.</li><li>Maintain accurate production records, logs, and documentation in plant systems.</li><li>Perform general warehouse duties such as staging materials, cleaning work areas, and organizing inventory.</li><li>Use basic computer systems and plant software to track production activities and update records.</li><li>Support continuous improvement efforts by identifying opportunities to enhance safety, quality, and efficiency.</li></ul>Essential Skills<ul><li>High school diploma or GED.</li><li>Ability to work effectively in a fast-paced production environment.</li><li>Basic computer skills for operating plant software and recording production data.</li><li>Strong attention to detail with a consistent focus on safety and quality.</li><li>Ability to communicate clearly and work collaboratively as part of a team.</li><li>Physical ability to lift, push, pull, and carry up to 65 pounds.</li><li>Ability to stand, walk, bend, and perform repetitive tasks throughout the shift.</li><li>Capability to work in an active warehouse environment with ongoing production activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree, technical certification, or vocational training in a related field.</li><li>1–2 years of experience in manufacturing, warehouse, agricultural, or production environments.</li><li>Experience working in agriculture, seed production, or seed quality operations.</li><li>Coursework in biology, agricultural science, or related laboratory work.</li><li>Experience with SAP or other production tracking and enterprise resource planning systems.</li><li>Experience documenting production or quality data in electronic or paper-based systems.</li><li>Familiarity with quality control processes and basic QA/QC principles in a production setting.</li><li>Comfort working with warehouse equipment and material handling processes.</li></ul>Work EnvironmentThis role is based in an active warehouse and seed production facility operating under ambient conditions without full climate control, so temperatures may vary with the seasons. You work around seed cleaning, treatment, packaging, and material handling equipment in a high-throughput environment that processes more than 3 million seed units annually. Personal Protective Equipment (PPE), including safety glasses, is required, and additional PPE such as hearing protection or respiratory protection may be required depending on specific tasks. Long pants and sleeves may be required in designated work areas to meet safety and protection standards. The facility operates on a 24-hour production schedule during peak season, and you must be available for day, evening, and overnight shifts, as well as overtime, weekend, and holiday work as needed. Work schedules may change during the season based on operational needs, and initial assignments may begin on a single shift before transitioning to multi-shift operations. The environment is team-oriented, offering the opportunity to gain valuable experience in manufacturing, warehouse operations, and agricultural production while contributing to food and agriculture innovation.Job Type &amp; LocationThis is a Contract position based out of Centralia, 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)Workplace TypeThis is a fully onsite position in Centralia,IL.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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.

<h2 style="text-align:center;">Seasonal Soy Bean Production Specialist</h2>Job DescriptionThe Seasonal Soy Bean Production Specialist supports a high-volume seed production facility during peak harvest and seed processing season. You operate and monitor seed cleaning, treatment, packaging, and shipping processes while maintaining strict safety, quality, and operational standards. This is a hands-on production role in a warehouse environment that requires flexibility to work across a 24-hour production schedule, including day, evening, overnight, weekend, and overtime shifts as business needs evolve.Responsibilities<ul><li>Operate and monitor seed cleaning, treatment, and packaging equipment using plant software systems.</li><li>Support daily seed processing activities to meet production, quality, and throughput goals.</li><li>Perform routine equipment inspections and basic troubleshooting to identify issues and minimize downtime.</li><li>Carry out preventive maintenance activities in accordance with established procedures.</li><li>Collect, record, and verify quality assurance and quality control (QA/QC) data for seed processing operations.</li><li>Follow all Standard Operating Procedures (SOPs), safety protocols, and applicable regulatory requirements.</li><li>Assist with material handling activities, including seed receiving, storage, shipping, and packaging.</li><li>Work collaboratively with production team members and site leadership to maintain efficient and safe operations.</li><li>Maintain accurate production records, logs, and documentation in plant systems.</li><li>Perform general warehouse duties such as staging materials, cleaning work areas, and organizing inventory.</li><li>Use basic computer systems and plant software to track production activities and update records.</li><li>Support continuous improvement efforts by identifying opportunities to enhance safety, quality, and efficiency.</li></ul>Essential Skills<ul><li>High school diploma or GED.</li><li>Ability to work effectively in a fast-paced production environment.</li><li>Basic computer skills for operating plant software and recording production data.</li><li>Strong attention to detail with a consistent focus on safety and quality.</li><li>Ability to communicate clearly and work collaboratively as part of a team.</li><li>Physical ability to lift, push, pull, and carry up to 65 pounds.</li><li>Ability to stand, walk, bend, and perform repetitive tasks throughout the shift.</li><li>Capability to work in an active warehouse environment with ongoing production activities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree, technical certification, or vocational training in a related field.</li><li>1–2 years of experience in manufacturing, warehouse, agricultural, or production environments.</li><li>Experience working in agriculture, seed production, or seed quality operations.</li><li>Coursework in biology, agricultural science, or related laboratory work.</li><li>Experience with SAP or other production tracking and enterprise resource planning systems.</li><li>Experience documenting production or quality data in electronic or paper-based systems.</li><li>Familiarity with quality control processes and basic QA/QC principles in a production setting.</li><li>Comfort working with warehouse equipment and material handling processes.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Centralia, 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)Workplace TypeThis is a fully onsite position in Centralia,IL.Application DeadlineThis position is anticipated to close on Sep 23, 2026.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: Segmentation Specialist Job DescriptionThe Segmentation Specialist serves as a highly proficient, quality-focused producer of pre-operative surgical plans for robotic-assisted total hip and total knee replacement procedures. This role centers on accurately reviewing and segmenting CT scans to create detailed 3D anatomical bone models, developing pre-operative plans, and ensuring all work meets established protocols and production targets. The position requires strong technical skills, attention to detail, and the ability to follow standardized procedures to deliver consistent, high-quality outputs.Responsibilities<ul><li>Create case records using a proprietary case management system to support pre-operative planning workflows.</li><li>Review CT scans to ensure they conform to established surgical protocols for robotic procedures.</li><li>Segment CT scans using specialized software to generate precise 3D anatomical bone models for use in robotic surgery.</li><li>Develop pre-operative surgical plans using digital bone models for robotically assisted total hip and total knee replacement procedures.</li><li>Review CT segmentations and surgical plans to verify the accuracy of anatomical landmark selection, implant sizing, and implant positioning.</li><li>Upload completed pre-operative plans to field-based personnel in a timely and accurate manner.</li><li>Document all activities according to prescribed methods, procedures, and work instructions.</li><li>Follow detailed work instructions exactly to deliver consistent, high-quality output and meet team and department production targets.</li><li>Apply efficient work methods to manage multiple cases and tasks in a fast-paced environment while maintaining quality standards.</li><li>Communicate effectively with internal stakeholders and demonstrate a strong customer service orientation in all interactions.</li></ul><h3>Required</h3><ul><li>Bachelor's degree in:<ul><li>Biological Sciences</li><li>Life Sciences</li><li>Biomedical Engineering</li><li>Biomedical Sciences</li><li>Anatomy</li><li>Biotechnology</li><li>Medical Imaging</li><li>Radiologic Sciences</li><li>Healthcare Sciences</li><li>Or a related scientific discipline</li></ul></li><li>Strong attention to detail and ability to follow structured processes.</li><li>Effective communication and organizational skills.</li><li>Proficiency with Microsoft Office applications.</li><li>Ability to work in a fast-paced, team-oriented environment.</li></ul><h3>We Also Welcome Candidates With</h3><ul><li>Externship, co-op, research, laboratory, clinical rotation, or academic project experience.</li><li>Exposure to CT, MRI, X-ray, or other medical imaging technologies.</li><li>Anatomy coursework or healthcare-related training.</li><li>Experience gained through university projects or research programs.</li></ul>INTERESTED IN THIS ROLE? SEE BELOW TO BE IMMEDIATELY CONSIDERED:<ul><li>I am scheduling phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Fathima</li><li>HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to fam@actalentservices.com or CALL- 904 530 5415</li></ul> Job Type &amp; LocationThis is a Contract position based out of Weston, FL.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)Workplace TypeThis is a fully onsite position in Weston,FL.Application DeadlineThis position is anticipated to close on Sep 11, 2026.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.

Segmentation Specialist .

Job Title: Segmentation TechnicianJob DescriptionThe Segmentation Technician plays a key role in producing high-quality pre-operative surgical plans that support robotically assisted total hip and knee replacement procedures. This role focuses on precise CT scan review, anatomical segmentation, and creation of digital 3D bone models using specialized software. You will contribute directly to cutting-edge medical device technology while working in a close-knit, collaborative team environment.Responsibilities<ul><li>Create new surgical cases using a proprietary case management system, ensuring all required information is accurately entered and organized.</li><li>Review CT scans for conformity to established surgical protocols and identify any issues that may impact the quality of the pre-operative plan.</li><li>Segment CT scans using specialized software to generate accurate 3D anatomical bone models for use in robotic surgery.</li><li>Develop pre-operative surgical plans based on the digital bone models for robotically assisted total hip and total knee replacement procedures.</li><li>Review CT segmentations and surgical plans for accuracy, including verification of anatomical landmark selection, implant sizing, and implant positioning.</li><li>Upload completed pre-operative plans to field-based personnel in a timely and organized manner to support surgical scheduling and preparation.</li><li>Document all activities and case details according to prescribed methods and procedures to maintain clear records and ensure compliance with internal standards.</li><li>Follow detailed work instructions precisely to deliver consistent, high-quality output and meet team and department production targets.</li><li>Maintain a strong individual focus on productivity and quality to support overall team performance and departmental goals.</li></ul>Essential Skills<ul><li>High school diploma is required; an associate degree or higher is preferred, ideally in a STEM-related field.</li><li>At least 2 years of work experience, preferably in fast-paced environments or computer-oriented roles.</li><li>Strong computer skills, including proficiency with design-related software; experience with tools such as Photoshop, CAD, or similar applications is preferred.</li><li>Ability to work with specialized segmentation software to create accurate 3D anatomical bone models.</li><li>Attention to detail and strong quality focus when reviewing CT scans, anatomical landmarks, and implant sizing and positioning.</li><li>Ability to follow detailed work instructions and standardized procedures consistently.</li><li>Solid documentation skills to record activities according to prescribed methods and processes.</li><li>Comfort working with medical and technical information, including CT imaging and surgical planning workflows.</li></ul>Additional Skills &amp; Qualifications<ul><li>Anatomy knowledge is highly preferred and will support accurate segmentation and surgical planning.</li><li>Background or coursework in biomedical fields, biology, microbiology, or related disciplines is beneficial.</li><li>Experience or skills in design, drafting, or graphic design, including familiarity with Adobe Illustrator or similar tools, are advantageous.</li><li>Prior exposure to medical environments, medical scribing, or working with medical imaging is helpful.</li><li>Strong general computer literacy and ability to learn proprietary case management and segmentation software.</li><li>Interest in biomedical technology and medical devices, particularly robotic surgery and joint replacement.</li><li>Motivation to grow into roles such as engineering, sales, onsite robotic surgery representative, or advanced positions within the department.</li></ul>Work EnvironmentThis is an in-office position in a relatively quiet, focused atmosphere. The standard schedule is first shift, Monday through Friday, from 7:00 a.m. to 3:30 p.m., with voluntary overtime opportunities of up to 10 hours. During the holiday season, Saturday work is typically available and Sunday shifts may be compensated at a higher rate. The team operates with a close-knit, family-style culture, emphasizing collaboration, support, and professional growth. Business casual dress attire is expected. You will work with proprietary case management systems and specialized segmentation software as part of a cutting-edge technology platform that is one of the largest growth drivers in the medical device industry, offering opportunities for career advancement into engineering, sales, onsite robotic surgery representation, and promotional roles within the department.Job Type &amp; LocationThis is a Contract position based out of Portage, MI.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)Workplace TypeThis is a fully onsite position in Portage,MI.Application DeadlineThis position is anticipated to close on Sep 16, 2026.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.

Segmentation Technician

Job Title: Surgical Scheduler/Senior Administrative AssistantJob DescriptionA leading academic healthcare organization seeks a skilled Surgical Scheduler for the Division of Otolaryngology (ENT) located in New Haven County, CT. This role demands a highly organized professional experienced in coordinating surgical procedures, managing provider schedules, and ensuring exceptional patient service. The position offers a Monday to Friday day shift schedule with the potential for hybrid work flexibility after approximately three months based on performance and training progress.Responsibilities<ul><li>Coordinate surgical procedures, clinic appointments, diagnostic testing, and post-operative visits.</li><li>Utilize EPIC to manage and prioritize scheduling requests while ensuring accuracy and efficiency.</li><li>Coordinate surgical documentation, pre-operative requirements, and follow-up care.</li><li>Build and maintain provider schedules, adjusting for time off, emergencies, and schedule changes.</li><li>Communicate appointment updates, cancellations, and scheduling changes to patients.</li><li>Verify insurance, referrals, and patient demographic information.</li><li>Maintain accurate patient records and documentation within the electronic medical record system.</li><li>Generate reports, compile clinical data, and support departmental administrative functions.</li><li>Coordinate meetings, conferences, and provider calendars as needed.</li><li>Provide exceptional customer service to patients, providers, and referring offices.</li><li>Support front desk and administrative operations as required.</li></ul>Essential Skills<ul><li>3+ years of medical scheduling experience.</li><li>Previous surgical scheduling experience.</li><li>Experience working within EPIC.</li><li>Strong knowledge of insurance verification, referrals, and medical office workflows.</li><li>Excellent organizational, communication, and customer service skills.</li><li>Ability to manage multiple priorities in a fast-paced clinical environment.</li><li>Experience supporting provider schedules and coordinating complex patient appointments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Proficiency in EPIC.</li><li>Skills in surgery scheduling, healthcare, appointment scheduling, calendar management, and administrative support.</li></ul>Work EnvironmentThis position is situated in a dynamic healthcare environment with a day shift schedule from 8:00 AM to 5:00 PM, Monday through Friday. After approximately three months, hybrid work flexibility may be available based on performance and training progress. The work involves collaborating with a diverse team in a fast-paced clinical setting, utilizing modern electronic medical record systems and communication tools to deliver top-quality care and coordination.If interested please book a virtual meeting with me here: https://talentassistant.actalentservices.com/assistant/bookings/bgF9HVktJob Type &amp; LocationThis is a Contract position based out of New Haven, CT.Pay and BenefitsThe pay range for this position is $25.00 - $32.00/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)Workplace TypeThis is a fully onsite position in New Haven,CT.Application DeadlineThis position is anticipated to close on Sep 11, 2026.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.

Senior Administrative Assistant

Job Title: Senior Associate – Analytical ChemistryJob DescriptionThis onsite Senior Associate role focuses on performing advanced analytical testing and protein characterization in a fast-paced laboratory environment. You contribute directly to method development, qualification, and data review using a range of chromatographic and electrophoretic techniques, while maintaining high standards of documentation, safety, and client service. This position is ideal for candidates with a bachelor’s degree in a scientific discipline and 1–3 years of hands-on industry experience in analytical testing and protein chemistry.Responsibilities<ul><li>Obtain assignments and follow the scientific direction provided by Senior scientific staff, flagging issues and seeking guidance when appropriate.</li><li>Perform analytical testing and data review using techniques such as HPLC/UHPLC (high and ultra-high performance liquid chromatography), ion exchange chromatography (IEX), size-exclusion chromatography (SEC), capillary electrophoresis, glycan mapping, peptide mapping, and mass spectrometry.</li><li>Execute method development and qualification studies, as well as protein characterization experiments, with guidance from Senior team members.</li><li>Demonstrate independence in day-to-day work and consistently produce high-quality, reliable results under minimal direction.</li><li>Generate complete, accurate, and concise documentation in electronic systems and laboratory notebooks, ensuring traceability and compliance.</li><li>Operate specialized laboratory equipment and instrumentation, including set-up, routine operation, and basic troubleshooting.</li><li>Perform general laboratory housekeeping activities to maintain a clean, organized, and safe work area.</li><li>Complete required training on assigned tasks and maintain up-to-date training records in accordance with site procedures.</li><li>Participate in quality improvement initiatives and contribute ideas to enhance laboratory processes and workflows.</li><li>Strive to deliver excellent service to internal and external clients by meeting timelines, communicating clearly, and addressing questions professionally.</li><li>Comply with safety guidelines and site-specific procedures, including proper use of building monitoring systems, maintenance of laboratory documentation, adherence to written procedures, and accurate completion of laboratory log books.</li><li>Support multiple project activities simultaneously in a highly matrixed team environment that may include Manufacturing, Process Development, Information Systems, Facilities, Engineering, and Quality Control.</li><li>Communicate issues or unexpected results promptly to Senior staff and collaborate on appropriate follow-up actions.</li><li>Address client questions independently when appropriate, using sound scientific judgment based on the work performed and reported.</li></ul>Essential Skills<ul><li>Bachelor’s degree (B.S. or equivalent) in Analytical Chemistry, Physical or Life Sciences, or a related technical discipline.</li><li>1–3 years of experience performing analytical testing in an industry or laboratory setting.</li><li>Hands-on experience executing analytical test methods using HPLC/UHPLC, ion exchange chromatography (IEX), size-exclusion chromatography (SEC), and related techniques.</li><li>Practical experience in protein chemistry, including method execution, troubleshooting, and interpretation of analytical data.</li><li>Ability to operate, maintain, and troubleshoot laboratory equipment and instrumentation used for analytical testing.</li><li>Strong laboratory documentation skills, including accurate, concise recording of data and procedures in electronic systems and laboratory notebooks.</li><li>Ability to work independently with minimal supervision while collaborating effectively as part of a cross-functional team.</li><li>Self-motivation, adaptability, and a positive attitude in a fast-paced, dynamic work environment.</li><li>Strong organizational and time management skills with the ability to handle multiple tasks and projects simultaneously.</li><li>Ability to learn new techniques quickly, follow detailed instructions, and comply with established laboratory and company policies.</li><li>Ability to respond to client inquiries with sound scientific judgment regarding analytical work and reported results.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience executing analytical test methods in one or more of the following areas: HPLC/UHPLC, ion exchange chromatography (IEX), size-exclusion chromatography (SEC), capillary electrophoresis, glycan mapping, peptide mapping, and mass spectrometry.</li><li>Understanding and application of principles, concepts, theories, and standards used in GMP and quality control microbiology laboratories.</li><li>Knowledge of regulatory and industry considerations related to analytical testing, including compliance issues and scientific discovery processes.</li><li>Theoretical and practical knowledge of protein chemistry, including structural and functional characterization.</li><li>Experience working in a matrixed environment with cross-functional partners such as Manufacturing, Process Development, Information Systems, Facilities, Engineering, and Quality Control.</li><li>Demonstrated ability to contribute to quality improvement efforts and continuous process enhancement.</li><li>Comfort interacting with internal and external clients, providing clear communication on testing status, results, and technical considerations.</li></ul>Work EnvironmentThis position is 100% onsite at a headquarters laboratory facility in Thousand Oaks, with a typical schedule of 8:30 a.m. to 5:30 p.m. The work is performed in a fast-paced, dynamic analytical laboratory environment that uses advanced technologies such as HPLC/UHPLC, ion exchange chromatography (IEX), size-exclusion chromatography (SEC), capillary electrophoresis, glycan mapping, peptide mapping, and mass spectrometry. You work closely with cross-functional teams, including Manufacturing, Process Development, Information Systems, Facilities, Engineering, and Quality Control, in a highly matrixed setting. The role requires regular use of specialized laboratory equipment and electronic documentation systems, adherence to detailed safety and compliance procedures, and participation in building and laboratory monitoring processes. The environment emphasizes strong collaboration, high energy, and continuous learning, with a focus on quality, client service, and maintaining an organized, well-kept laboratory space.Job Type &amp; LocationThis is a Contract position based out of Thousand Oaks, CA.Pay and BenefitsThe pay range for this position is $26.00 - $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)Workplace TypeThis is a fully onsite position in Thousand Oaks,CA.Application DeadlineThis position is anticipated to close on Sep 25, 2026.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.

Senior Associate

Senior Beverage TechnologistPosition SummaryWe are seeking a Senior Beverage Technologist to lead the development and commercialization of innovative beverage solutions, including ready-to-drink, ready-to-mix, and plant-based products. This role combines hands-on formulation, pilot plant support, customer engagement, and cross-functional collaboration to bring beverage concepts from idea to market.Key Responsibilities<ul><li>Develop beverage formulations for customer projects, demonstrations, and trade shows.</li><li>Lead projects from concept through pilot trials, scale-up, and commercialization.</li><li>Provide technical support on labeling, regulatory requirements, and ingredient selection.</li><li>Conduct sensory evaluations, product tastings, and formulation optimization.</li><li>Deliver customer presentations and product demonstrations.</li><li>Collaborate with customers and internal teams to develop market-ready beverage solutions.</li><li>Maintain accurate project documentation and GMP-compliant laboratory practices.</li><li>Support team development through mentorship and knowledge sharing.</li></ul>Qualifications<ul><li>Bachelor's degree in Food Science, Physical Sciences, or a related field.</li><li>5-8 years of beverage product development or applications experience.</li><li>Experience with RTD, RTM, plant-based, carbonated, functional, alcoholic, and UHT beverages.</li><li>Strong knowledge of beverage processing, scale-up, and commercialization.</li><li>Understanding of labeling regulations and ingredient functionality.</li><li>Experience conducting sensory evaluations and interpreting results.</li><li>Strong communication, presentation, project management, and customer-facing skills.</li></ul>Preferred Qualifications<ul><li>Experience with sports drinks, juice beverages, and dry beverage mixes.</li><li>Familiarity with UHT systems, carbonators, pasteurizers, and Microthermics equipment.</li><li>Strong laboratory organization and raw material management skills.</li><li>Interest in growing into leadership and mentorship responsibilities.</li></ul>Work Environment GMP-regulated laboratory and production environment with routine product tasting and sensory evaluation. Exposure to food allergens is expected. Ability to stand for extended periods and occasionally lift up to 30 lbs. Standard daytime schedule with collaboration across a small, highly interactive applications team.Job Type &amp; LocationThis is a Contract to Hire position based out of Addison, IL.Pay and BenefitsThe pay range for this position is $26.00 - $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)Workplace TypeThis is a fully onsite position in Addison,IL.Application DeadlineThis position is anticipated to close on Sep 18, 2026.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.

Senior Beverage Technologist

Job Title: Senior Factory BuyerJob DescriptionThe Senior Factory Buyer plays a critical role in supporting production operations in a high-volume manufacturing environment. This onsite position partners closely with manufacturing, planning, and supply chain teams to ensure that materials are available to meet production demands while balancing inventory, cost, and delivery objectives. In addition to executing procurement strategies and managing supplier relationships, the Senior Factory Buyer uses data analysis to identify trends, optimize inventory performance, support cost reduction initiatives, and develop actionable insights that inform business decisions. The role offers strong visibility with leadership and requires the ability to analyze complex supply chain data, present clear findings and recommendations, and drive continuous improvement efforts that directly impact factory performance. This opportunity is ideal for someone who thrives in a dynamic manufacturing setting and enjoys combining strategic purchasing, analytics, and cross-functional collaboration, with potential to grow into a manager role over time.Responsibilities<ul><li>Partner closely with manufacturing, planning, and supply chain teams to ensure timely availability of materials that meet production schedules and demand.</li><li>Execute purchasing activities in a high-volume manufacturing environment, including creating, managing, and tracking purchase orders.</li><li>Manage supplier relationships to ensure reliable delivery performance, quality, and cost effectiveness across all sourced materials.</li><li>Balance inventory levels, cost targets, and delivery requirements to support production while minimizing excess stock and stockouts.</li><li>Leverage data analysis to identify trends in material usage, supplier performance, and inventory metrics, and translate findings into actionable insights.</li><li>Optimize inventory performance by monitoring key indicators, adjusting purchasing strategies, and supporting initiatives that reduce inventory risk and cost.</li><li>Support cost reduction initiatives by identifying opportunities for savings, negotiating with suppliers, and recommending alternative sourcing options where appropriate.</li><li>Analyze complex supply chain data and present clear, concise findings and recommendations to leadership and cross-functional stakeholders.</li><li>Drive continuous improvement efforts in procurement processes, supplier management, and inventory control to enhance overall factory performance.</li><li>Collaborate with internal teams to resolve material availability issues, expedite critical orders, and maintain smooth production operations.</li><li>Ensure purchasing activities comply with requirements for medical device, pharmaceutical, or other regulated environments, as applicable.</li><li>Use SAP and related systems to manage purchasing transactions, maintain accurate records, and generate reports that support decision-making.</li></ul>Essential Skills<ul><li>Minimum of 4 years of experience as a buyer or purchaser.</li><li>Proven experience purchasing in a high-volume manufacturing environment.</li><li>Experience purchasing in medical device, pharmaceuticals, or other regulated environments.</li><li>Strong purchasing and procurement skills, including creating and managing purchase orders.</li><li>Working knowledge of SAP for purchasing and inventory-related activities.</li><li>Familiarity with APICS concepts or frameworks related to planning and supply chain management.</li><li>Ability to analyze supply chain and inventory data to identify trends and develop insights.</li><li>Experience collaborating with manufacturing, planning, and supply chain teams.</li><li>Demonstrated ability to balance inventory levels, cost objectives, and delivery requirements.</li></ul>Additional Skills &amp; Qualifications<ul><li>Background in purchasing within medical device or pharmaceutical manufacturing is highly beneficial.</li><li>Experience working in a regulated environment and adhering to related processes and standards.</li><li>Comfort working with high-volume purchasing and fast-paced production operations.</li><li>Ability to present data-driven findings and recommendations to leadership and cross-functional stakeholders.</li><li>Interest in career growth with potential to move into a manager role within approximately 3–5 years.</li><li>Strong analytical mindset with a focus on continuous improvement in procurement and inventory management.</li></ul>Work EnvironmentThis role is based 100% onsite in a manufacturing facility in Littleton, working closely with production operations on a daily basis. The Senior Factory Buyer collaborates with two other buyers and cross-functional teams in manufacturing, planning, and supply chain. The environment is dynamic and fast-paced, with a focus on high-volume production and regulated processes, particularly in areas such as medical devices or pharmaceuticals. SAP and other manufacturing and planning tools are used regularly to manage purchasing activities, inventory data, and reporting. The onsite setting supports frequent interaction with colleagues on the factory floor and in office areas, fostering close teamwork and direct visibility into production needs and performance.Job Type &amp; LocationThis is a Permanent position based out of Lakewood, CO.Pay and BenefitsThe pay range for this position is $70000.00 - $98000.00/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.Terumo Blood and Cell Technologies is part of Terumo Group, founded in 1921 and headquartered in Tokyo, Japan.
In 2024, Terumo Blood and Cell Technologies reached $1.5 billion in revenue.
We employ nearly 8,000 associates globally, with global headquarters in Lakewood, CO, U.S., and regional headquarters in Brussels, Buenos Aires, Singapore and Tokyo.
We manufacture devices, disposable sets and solutions at our facilities in Belgium, India, Japan, Northern Ireland, the U.S. and Vietnam. Our global presence enables us to serve customers in more than 130 countries.
Our core values help set our direction, guide our actions and keep us true to our corporate mission of contributing to society through healthcare.
Respect – Appreciative of others
Integrity – Guided by our mission
Care – Empathetic to patients
Quality – Committed to excellence
Creativity – Striving for innovation
We contribute to the Leukemia and Lymphoma Society (LLS), raising $2.4 million USD since 2025.Workplace TypeThis is a fully onsite position in Lakewood,CO.Application DeadlineThis position is anticipated to close on Sep 25, 2026.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.

Senior Buyer

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