Job Title: Case ManagerJob DescriptionThe Case Manager is responsible for identifying complex cases based on enrollment criteria and managing a caseload of assigned members. The role requires performing routine follow-ups with patients, which may take place via phone, at the primary care provider’s office, in the patient's home, or other appropriate settings. The Case Manager will contact members after hospital discharge and ensure thorough documentation of interactions and outcomes within established timeframes.Responsibilities<ul><li>Identify complex cases based on enrollment criteria.</li><li>Monitor and manage assigned member caseloads.</li><li>Perform routine follow-ups with each patient in various settings.</li><li>Contact members post-hospital discharge and after transitional nurse visits.</li><li>Discuss program details with members and initiate the enrollment process.</li><li>Ensure documentation is thorough and completed within established timeframes.</li><li>Document actions taken to prevent readmission and other transitions of care.</li><li>Complete HRA required outreach within 30 days of eligibility or upload from health plan.</li><li>Develop and update an individualized plan of care with S.M.A.R.T. goals.</li><li>Collaborate with healthcare providers and staff to optimize care continuity.</li><li>Educate members about available organizational and community resources.</li><li>Mail out welcome packets including Resource Booklet information to members.</li><li>Obtain updated orders from healthcare providers to initiate services.</li><li>Submit orders with supporting documentation to the case management support team.</li><li>Attend Care Coordination IDT meetings and staff meetings.</li><li>Collaborate with the scheduling team for appropriate member scheduling.</li><li>Assist with processing referrals to expedite care and optimize health.</li><li>Submit communication forms and advanced directives according to departmental policies.</li><li>Stay updated on hospital discharge planning intervention expectations.</li></ul>Essential Skills<ul><li>Acute care experience.</li><li>Proficiency in case management and hospital settings.</li><li>Graduate of an accredited Licensed Vocational Nursing program.</li><li>Current LVN nursing license.</li><li>2 years of clinical nursing experience or 1 year of case management experience.</li><li>Knowledge of medical terminology.</li><li>Proficiency in Microsoft Office applications.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to utilize computers and software applications effectively.</li><li>Strong communication and organizational skills.</li></ul>Work EnvironmentThe position is a fully onsite role in an office environment, operating Monday through Friday from 8am to 5pm. This is a minimum 12-week assignment covering a leave of absence in the department. The dress code is scrubs.Job Type &amp; LocationThis is a Contract position based out of Victorville, CA.Pay and BenefitsThe pay range for this position is $24.19 - $31.45/hr.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 Victorville,CA.Application DeadlineThis position is anticipated to close on Jul 28, 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

LVN Case Manager

Job Title: Case ManagerJob DescriptionThe Case Manager is responsible for identifying complex cases based on enrollment criteria and managing a caseload of assigned members. The role requires performing routine follow-ups with patients, which may take place via phone, at the primary care provider’s office, in the patient's home, or other appropriate settings. The Case Manager will contact members after hospital discharge and ensure thorough documentation of interactions and outcomes within established timeframes.  Responsibilities<ul><li>Identify complex cases based on enrollment criteria.</li><li>Monitor and manage assigned member caseloads.</li><li>Perform routine follow-ups with each patient in various settings.</li><li>Contact members post-hospital discharge and after transitional nurse visits.</li><li>Discuss program details with members and initiate the enrollment process.</li><li>Ensure documentation is thorough and completed within established timeframes.</li><li>Document actions taken to prevent readmission and other transitions of care.</li><li>Complete HRA required outreach within 30 days of eligibility or upload from health plan.</li><li>Develop and update an individualized plan of care with S.M.A.R.T. goals.</li><li>Collaborate with healthcare providers and staff to optimize care continuity.</li><li>Educate members about available organizational and community resources.</li><li>Mail out welcome packets including Resource Booklet information to members.</li><li>Obtain updated orders from healthcare providers to initiate services.</li><li>Submit orders with supporting documentation to the case management support team.</li><li>Attend Care Coordination IDT meetings and staff meetings.</li><li>Collaborate with the scheduling team for appropriate member scheduling.</li><li>Assist with processing referrals to expedite care and optimize health.</li><li>Submit communication forms and advanced directives according to departmental policies.</li><li>Stay updated on hospital discharge planning intervention expectations.</li></ul>Esessential Skills <ul><li>Acute care experience.</li><li>Proficiency in case management and hospital settings.</li><li>Graduate of an accredited Licensed Vocational Nursing program.</li><li>Current LVN nursing license.</li><li>2 years of clinical nursing experience or 1 year of case management experience.</li><li>Knowledge of medical terminology.</li><li>Proficiency in Microsoft Office applications.</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to utilize computers and software applications effectively.</li><li>Strong communication and organizational skills.</li></ul>Work EnvironmentThe position is a fully onsite role in an office environment, operating Monday through Friday from 8am to 5pm. Job Type &amp; LocationThis is a Contract position based out of Victorville, CA.Pay and BenefitsThe pay range for this position is $24.19 - $31.45/hr.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 Victorville,CA.Application DeadlineThis position is anticipated to close on Aug 5, 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>Actively Screening for Lab Analyst to join global animal health company in Lithia Springs, GA!</h2>Job DescriptionThe Lab Analyst works in a fast-paced, customer-oriented team laboratory environment to analyze finished product samples prior to commercial release. This role is part of a dynamic, growing laboratory within an expanding manufacturing site, offering opportunities to learn new skills, collaborate cross-functionally, and contribute to the launch and ongoing production of innovative animal health medications.Responsibilities<ul><li>Prepare samples accurately and efficiently for analysis, following established laboratory procedures.</li><li>Operate a variety of laboratory equipment to perform qualitative and quantitative assays on finished product samples.</li><li>Perform, document, and record checks on all assays to ensure data integrity and compliance with applicable standards.</li><li>Interpret and evaluate analytical data for accuracy, precision, trends, and potential Good Manufacturing Practice (GMP) impact.</li><li>Maintain clear, accurate, and complete laboratory records in accordance with cGMP and internal documentation requirements.</li><li>Recommend and execute process improvements to continually enhance laboratory performance, efficiency, and reliability.</li><li>Demonstrate high productivity and the ability to multi-task while maintaining a low error rate and strong attention to detail.</li><li>Apply good laboratory techniques at all times to avoid cross-contamination or misidentification of samples.</li><li>Follow written procedures and standard operating procedures (SOPs) consistently and precisely.</li><li>Participate in manufacturing quality control support activities, such as cleaning verification, as needed.</li><li>Collaborate closely with microbiologists, chemists, and other team members to support day-to-day laboratory operations.</li><li>Engage flexibly and proactively in a changing environment, adapting to new methods, technologies, and priorities.</li><li>Contribute to a culture of continuous learning, quality, and ownership within the laboratory and broader site.</li></ul>Essential Skills<ul><li>Minimum of 1 year of industry laboratory testing experience in a regulated environment such as pharmaceutical, chemical, medical device, food and beverage, microbiology, or environmental monitoring.</li><li>Demonstrated experience performing qualitative and quantitative laboratory assays.</li><li>Ability to interpret and evaluate analytical data for accuracy, precision, and trends.</li><li>Strong attention to detail with a proven ability to maintain a low error rate while managing multiple tasks.</li><li>Ability to follow written procedures and standard operating procedures accurately.</li><li>Good laboratory technique, including practices that prevent cross-contamination and sample misidentification.</li><li>Experience working in a team-oriented laboratory environment with a customer-focused mindset.</li><li>Willingness and ability to learn new methods, technologies, and processes.</li><li>Effective communication skills to document results clearly and collaborate with cross-functional teams.</li><li>Understanding of cGMP principles and their application in a manufacturing laboratory setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline preferred.</li><li>Experience in pharmaceutical or biopharmaceutical manufacturing environments is advantageous.</li><li>Familiarity with laboratory techniques such as UV-Vis spectroscopy, pH measurement, conductivity testing, ELISA, and microbiological methods.</li><li>Exposure to environmental monitoring practices in a manufacturing or laboratory setting.</li><li>Experience using laboratory data systems such as Empower or similar platforms is beneficial.</li><li>Ability to work effectively in a large, cross-functional team and contribute to a collaborative culture.</li><li>Strong problem-solving mindset with the ability to recommend and support process improvements.</li><li>Ownership mentality and comfort working in a new, rapidly evolving site with growing capabilities.</li></ul>Work EnvironmentThis role is based in a brand-new, approximately 640,000-square-foot manufacturing and laboratory facility in Lithia Springs, GA. The plant has completed construction and the laboratories are fully built out, providing modern equipment and infrastructure to support microbiologists, chemists, and other scientific staff in their daily activities. The site focuses on manufacturing advanced animal health products, including monoclonal antibody therapies, and is in a growth phase with significant opportunity to shape processes and culture. Working hours follow a roughly Monday through Friday schedule, around 8:00 a.m. to 5:00 p.m., with some flexibility to accommodate local traffic patterns and late afternoon meetings, which are common. The environment emphasizes teamwork, continuous learning, and an ownership mentality as the site scales up production. During the contract period, team members receive 6 paid holidays and 40 hours of paid time off (PTO). Dress code aligns with standard laboratory and manufacturing safety requirements, including appropriate attire and use of personal protective equipment as needed for work in lab and production areas.Job Type &amp; LocationThis is a Contract position based out of Lithia Springs, GA.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/hr.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 Lithia Springs,GA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Analyst

Job Title: Lab AssistantJob DescriptionThe Lab Assistant (Production Lab Assistant) supports the processing of raw biological materials, primarily cow and pig blood, to produce high-quality components used in the manufacture of calibrators for hematology instruments. This role focuses on operating centrifuges to separate red and white blood cells, maintaining and cleaning production equipment, and completing accurate documentation in an FDA-regulated environment. The position is hands-on, highly process-oriented, and offers strong exposure to laboratory manufacturing workflows and systems.Responsibilities<ul><li>Operate centrifuges to process raw animal blood and separate red and white blood cells for further use in downstream components labs.</li><li>Handle and process large volumes of cow and pig blood in accordance with standard operating procedures and safety guidelines.</li><li>Maintain, clean, and prepare production equipment and containers after processing runs to ensure readiness for future batches.</li><li>Wash, rinse, and handle dishware and lab equipment, ensuring all items are properly cleaned and maintained.</li><li>Wrap cleaned equipment for further sterilization, following established protocols to maintain a controlled and compliant environment.</li><li>Batch and label products accurately, ensuring correct lot numbers and identifiers are applied to all materials.</li><li>Document results, processes, and observations thoroughly, including referencing and updating past batch records as required.</li><li>Follow standard operating procedures (SOPs) and adhere to appropriate lab protocols, including regulatory requirements related to chemical handling, hazards, and equipment use.</li><li>Comply with all FDA regulations and internal documentation standards to support traceability and quality control.</li><li>Follow daily work instructions and priorities set by the supervisor, maintaining a strong commitment to safety and quality.</li><li>Participate in continuous process improvement efforts by identifying, communicating, and helping to address areas for operational or quality enhancement.</li><li>Work both independently and as part of a team to complete daily production and lab tasks efficiently.</li><li>Perform additional duties as assigned to support lab operations and production goals.</li></ul>Essential Skills<ul><li>Experience working in a general laboratory or production lab environment.</li><li>Strong attention to detail, especially when following SOPs, documenting processes, and labeling products.</li><li>Ability to accurately complete documentation and maintain batch records in a regulated setting.</li><li>Comfort working directly with pig and cow blood and other raw biological materials.</li><li>Ability to follow standard operating procedures (SOPs) consistently and precisely.</li><li>Capability to work both independently and as part of a team, as verified by references.</li><li>Basic math skills sufficient to perform dilutions and related calculations.</li><li>Awareness of chemical handling protocols, hazards, and safe use of laboratory equipment.</li><li>Physical ability to stand and move throughout the lab and dishwashing areas for the majority of the workday.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in a science-related field (preferred).</li><li>Prior experience in an FDA-regulated laboratory or production environment.</li><li>Familiarity with hematology-related processes or calibrator production is an advantage.</li><li>Interest in career growth within a large scientific manufacturing organization, including potential promotion into manufacturing labs or other internal departments.</li><li>Demonstrated ability to follow detailed written and verbal instructions.</li><li>Strong commitment to safety, quality, and continuous improvement.</li></ul>Work EnvironmentThe Lab Assistant works in a clean, FDA-regulated raw materials laboratory located in a well-lit basement facility. The role is fully on-site with no remote work available. Lab assistants spend the majority of their day on their feet, moving between the lab space and dishwashing area while operating centrifuges and handling equipment. The environment involves frequent handling of large quantities of cow and pig blood to separate red and white blood cells. Standard lab attire includes a lab coat, goggles, and hairnet, and appropriate personal protective equipment is required at all times. Employees may wear headphones while working, as permitted by safety guidelines. The schedule is Monday through Friday from 8:00 a.m. to 4:30 p.m., with little overtime or weekend work, providing a consistent daytime shift in a structured and process-driven setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.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 Minneapolis,MN.Application DeadlineThis position is anticipated to close on Aug 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.

Lab Assistant

Job Title: Lab AssistantJob DescriptionThe primary role of a Lab Assistant is to process laboratory samples, predominantly blood, and work with other laboratory employees to catalog patient specimens such as blood, urine, or tissue for analysis. Lab professionals play a critical role in diagnosis and treatment based on the samples received.Responsibilities<ul><li>Receive and triage all specimens for clinical testing.</li><li>Manage clinical information within the Laboratory Information Management System (LIMS) database.</li><li>Perform internal audits of clinical charts.</li><li>Collaborate with various departments to ensure testing accuracy.</li><li>Pull urine or other specimens for analysis and aliquot them at required volumes for accurate testing.</li><li>Store specimens in refrigerated or freezer storage, spending extensive time in walk-in units.</li><li>Verify specimens for testing in accordance with Standard Operating Procedure.</li><li>Perform other administrative duties as assigned by the supervisor.</li></ul>Essential Skills<ul><li>Proven attention to accuracy and deadlines.</li><li>Ability to work well independently and within a team.</li><li>0-2 years of experience in a similar role.</li></ul>Additional Skills &amp; Qualifications<ul><li>AS or BS degree in biological sciences preferred.</li><li>Comfortable working in a freezer and handling bodily fluids.</li><li>Detail-oriented and able to multi-task.</li><li>Experience with labeling, aliquoting, laboratory data entry, and specimen collection.</li></ul>Work EnvironmentThe position is based in a laboratory environment, working primarily during the third shift from 10 PM to 6:30 AM. The lab team consists of six members on this shift. Staff must dress accordingly due to time spent in refrigerated or freezer storage units. The role involves handling bodily fluids, and adherence to safety protocols is essential. This position is an opportunity to work within a large diagnostics company.Job Type &amp; LocationThis is a Contract to Hire position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $18.00 - $20.00/hr.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 Raleigh,NC.Application DeadlineThis position is anticipated to close on Jul 31, 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>Lab Assistant</h2>Job DescriptionWe are seeking a dedicated Lab Assistant to support our manufacturing operations. This role involves conducting daily batch and physical testing, operating laboratory computers and analytical instruments, and ensuring the quality of incoming raw materials. The Lab Assistant will document analytical data and audit information, assist in investigating material anomalies, and support plant trial requests. The successful candidate will adhere to good laboratory practices and perform cleaning and housekeeping tasks in the laboratory.Responsibilities<ul><li>Conduct daily batch and physical testing using standard chemical assays.</li><li>Operate laboratory computers and analytical instruments, including troubleshooting and calibrations.</li><li>Test incoming raw materials and verify quality against benchmarks.</li><li>Document analytical data, audit information, and specifications in data management systems.</li><li>Assist in investigating non-chemical material anomalies in manufacturing.</li><li>Support plant trial requests as needed.</li><li>Adhere to good laboratory practices for safe chemical handling.</li><li>Perform cleaning and housekeeping tasks for the laboratory and equipment.</li><li>Collaborate with chemists on additional duties.</li><li>Ensure regular and predictable attendance.</li></ul>Essential Skills<ul><li>1+ years of experience in a lab or testing environment with wet chemistry procedures.</li><li>Experience in medical, manufacturing, or food lab settings.</li><li>Ability to troubleshoot and calibrate laboratory equipment.</li><li>Experience in a manufacturing environment and chemical handling.</li><li>Proficiency in batch testing and wet chemistry.</li></ul>Additional Skills &amp; Qualifications<ul><li>Open to candidates with or without a degree.</li><li>Strong oral and written communication skills.</li><li>Proficiency in Microsoft Word and Excel.</li><li>Good organizational and time management skills.</li><li>Ability to work a flexible schedule.</li><li>Knowledge of HPLCs is a plus.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Harrisonville, MO.Pay and BenefitsThe pay range for this position is $18.00 - $21.00/hr.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 Harrisonville,MO.Application DeadlineThis position is anticipated to close on Jul 27, 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: Laboratory Assistant Job DescriptionThis Laboratory Assistant role focuses on receiving, preparing, preserving, and disposing of samples while maintaining accurate records and supporting laboratory operations. You will work with a variety of materials, including hazardous substances, and help ensure that all samples are handled, stored, and processed according to established procedures and safety standards. This position offers the opportunity to contribute meaningful work to the community while building a long-term career in a fast-paced laboratory environment.Responsibilities<ul><li>Receive, sort, and accession incoming samples to ensure they are correctly identified, labeled, and logged into the system.</li><li>Retain and dispose of materials for the organization and its clients in accordance with established procedures and regulatory requirements.</li><li>Ensure all samples are properly stored, including moving them to appropriate storage units, laboratory areas, or trucks as needed.</li><li>Prepare samples for testing by performing sample prep activities such as aliquoting, mixing, and organizing specimens.</li><li>Add correct preservatives to samples when necessary to maintain sample integrity and suitability for analysis.</li><li>Handle hazardous materials safely, including crude oil, refined petroleum products, refined fuels such as gasoline, diesel, fuel oil, residual oil, LPG, petrochemicals, industrial gases, and natural gas.</li><li>Move approximately 20–50 boxes weekly between storage units, laboratory spaces, and vehicles, ensuring safe handling and organization.</li><li>Dispose of samples in accordance with standard operating procedures and safety guidelines.</li><li>Assist other laboratory personnel with analytical activities, including basic analysis tasks, data checks, and data approval processes.</li><li>Perform simple calculations related to sample preparation, testing, and data verification.</li><li>Maintain accurate and complete records of sample retention, disposal, and related activities.</li><li>Follow standard operating procedures (SOPs) consistently and accurately in all aspects of sample handling and laboratory work.</li><li>Support daily lab operations by helping process up to 100 samples per day in a fast-paced environment.</li><li>Collaborate with team members to ensure efficient workflow and timely completion of laboratory tasks.</li></ul>Essential Skills<ul><li>At least 6 months of experience in a production environment.</li><li>High school diploma or GED equivalent.</li><li>Experience with data entry related to laboratory or production processes.</li><li>Ability to perform sample sorting, accessioning, labeling, and basic specimen collection tasks.</li><li>Hands-on experience with sample preparation, including organizing, handling, and prepping samples for testing.</li><li>Understanding of sample preservation techniques and use of appropriate preservatives.</li><li>Ability to handle hazardous materials such as crude oil, refined petroleum products, refined fuels, LPG, petrochemicals, industrial gases, and natural gas in a safe and compliant manner.</li><li>Ability to lift and move boxes weighing up to 50 pounds on a regular basis.</li><li>Proven ability to follow standard operating procedures (SOPs), as demonstrated by previous work experience and references.</li><li>Strong attention to detail for accurate labeling, recordkeeping, and data checking.</li><li>Comfort working in a fast-paced environment processing high sample volumes.</li><li>Basic math skills to perform simple calculations related to laboratory tasks.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience in a laboratory assistant or similar lab support role.</li><li>Familiarity with chemistry concepts and laboratory workflows.</li><li>Experience supporting data review and approval processes in a lab setting.</li><li>Ability to work effectively as part of a team and communicate clearly with coworkers.</li><li>Strong organizational skills for managing multiple samples, records, and tasks simultaneously.</li><li>Interest in building a long-term career within an industry-recognized laboratory environment.</li></ul>Work EnvironmentThis position operates in a fast-paced laboratory setting, processing up to 100 samples daily. The standard schedule is Monday through Friday from 8:00 a.m. to 5:00 p.m. You will work closely with a team and handle a variety of materials, including hazardous substances such as crude oil, refined fuels, LPG, petrochemicals, industrial gases, and natural gas. The role involves regular physical activity, including moving 20–50 boxes per week and lifting up to 50 pounds. Lab safety attire, including lab coat, safety glasses, gloves, and other protective equipment, will be provided to support safe handling of samples and materials. The dress code requires a shirt that covers the stomach, lower back, and upper arms, long pants, and shoes that completely cover the feet. The organization offers strong medical, dental, and vision benefits, supplemental life coverage, a 401(k) match program (with eligibility after 30 days of employment), and generous vacation and sick time benefits. Employees have the opportunity to perform work that is meaningful to their community and to grow a career with an industry-recognized employer.Job Type &amp; LocationThis is a Contract position based out of Sulphur, LA.Pay and BenefitsThe pay range for this position is $19.00 - $20.00/hr.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 Sulphur,LA.Application DeadlineThis position is anticipated to close on Jul 28, 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: Lab Assistant / PhlebotomistJob SummaryWe are looking for a Lab Assistant / Phlebotomist to support our clinic team. This role involves working directly with patients, performing blood draws, and assisting with basic lab tasks to keep operations running smoothly. Under the supervision of the Clinic Manager, the Laboratory Assistant (Phlebotomist) is responsible for supporting the licensed medical staff in a clinic setting with phlebotomy and routine tests including injections, immunizations, point of care tests, CLIA waived tests, etc., while maintaining high customer service standards. This position supports patient-centered care by working collaboratively to deliver timely results and follow-up for laboratory testing which supports optimal patient outcomes.Responsibilities<ul><li>Perform blood draws and collect specimens</li><li>Process and prepare lab samples</li><li>Update patient information in the electronic health record</li><li>Performs phlebotomy and processing of specimens to be sent to outside laboratory.</li><li>Injects patients with medications after verification by a provider, to the extent permitted by law.</li><li>Performs finger sticks and TB skin tests.</li><li>Measures and describes skin test reaction in Electronic Health Record system (EHR) and reports to provider any reactions exceeding thresholds.</li><li>Performs CLIA waived In-House tests ordered by providers.</li><li>Maintains quality control of all In-House laboratory tests.</li></ul>Requirements<ul><li>Valid California Phlebotomy license</li><li>At least 2 years of prior experience in a medical care setting, including phlebotomy and injection experience and/or training, or an equivalent combination of education and experience</li><li>At least 1 year of phlebotomy or lab experience</li><li>Bilingual Spanish preferred</li></ul>Work EnvironmentOnsite clinic setting with a supportive team and opportunities for growth.Job Type &amp; LocationThis is a Contract to Hire position based out of Santa Barbara, CA.Pay and BenefitsThe pay range for this position is $28.00 - $28.00/hr.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 Santa Barbara,CA.Application DeadlineThis position is anticipated to close on Jul 10, 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.

Lab Assistant/ Phlebotomist

Job Title: Histology Lab AssociateJob DescriptionThe Histology Lab Associate supports daily histology laboratory operations by coordinating workflow, organizing specimens, handling slides, performing data entry, and providing broad laboratory support. This role serves as a key operational partner to histology, imaging, and biosample operations teams, helping highly skilled technical staff focus on sectioning, imaging, and scientific data generation. The position offers exposure to cutting-edge biotechnology research, histology workflows, imaging processes, and biosample management in a fast-paced research environment.Responsibilities<ul><li>Coordinate daily histology laboratory workflows to ensure smooth and timely processing of specimens and slides.</li><li>Print, label, and organize slides and tissue blocks with high accuracy to maintain sample integrity and traceability.</li><li>Accession specimens, enter data, and track samples throughout their lifecycle to support chain-of-custody and proper specimen management.</li><li>Manage laboratory records and databases to ensure accurate documentation and sample traceability in accordance with SOPs and laboratory requirements.</li><li>Coordinate the movement of samples between histology, imaging, and biosample operations to support efficient laboratory throughput.</li><li>Support staining workflows by preparing materials, organizing slides, and ensuring required reagents and supplies are available.</li><li>Assist with imaging processes by organizing slides, coordinating sample readiness, and supporting imaging operations as needed.</li><li>Organize laboratory materials, supplies, and inventory to keep the workspace efficient, safe, and well-stocked.</li><li>Monitor inventory and sample storage systems to ensure materials and specimens remain organized, accessible, and properly documented.</li><li>Use data entry tools, LIMS, and related laboratory systems to record, update, and retrieve information accurately.</li><li>Follow established SOPs, laboratory documentation requirements, and safety practices while handling biological specimens and working in regulated environments.</li><li>Independently identify tasks and operational needs, taking initiative to complete work that supports overall laboratory efficiency.</li><li>Collaborate closely with histology, imaging, biosample operations, and other laboratory teams, communicating effectively to coordinate activities and resolve issues.</li><li>Proactively identify opportunities to improve operational efficiency, streamline workflows, and enhance laboratory support processes.</li><li>Maintain a clean, organized, and compliant laboratory environment, contributing to a culture of operational excellence and accountability.</li></ul>Essential Skills<ul><li>Demonstrated laboratory operations experience that enables rapid contribution to daily histology and biospecimen workflows.</li><li>Proficiency in sample accessioning and tracking to maintain chain-of-custody and effective specimen management.</li><li>Strong data entry and database management skills to support accurate record keeping and sample traceability.</li><li>Exceptional attention to detail for maintaining sample integrity, labeling accuracy, and overall workflow quality.</li><li>Advanced organizational skills to manage multiple histology workflows and tasks simultaneously in a fast-paced environment.</li><li>Self-starter mentality with the ability to independently identify work that needs to be completed and take initiative.</li><li>Collaborative mindset with the ability to support multiple laboratory functions and stakeholders effectively.</li><li>Experience with inventory and sample management to ensure materials and specimens remain organized and accessible.</li><li>Clear and professional communication skills for coordinating with histology, imaging, and biosample teams.</li><li>Experience following SOPs and laboratory documentation requirements.</li><li>Ability to stand for extended periods while performing laboratory duties.</li><li>Ability to handle biological specimens according to established procedures and safety standards.</li><li>Familiarity with laboratory safety practices and working safely with biological materials.</li><li>Experience using Microsoft Office Suite for documentation, tracking, and communication.</li><li>Comfort working in fast-paced, research-focused laboratory environments.</li></ul>Work EnvironmentThis role operates in a fast-paced biotechnology research environment that supports histology, imaging, and biospecimen workflows. Team members work closely together and value initiative, accountability, collaboration, and operational excellence. The culture rewards individuals who identify problems, offer solutions, and proactively support the success of others. You will work with laboratory information management systems such as LIMS and Benchling, and handle tissue samples and imaging-related workflows. The environment offers strong visibility across multiple functional teams, opportunities for long-term growth within laboratory operations, and direct impact on scientific productivity and data generation. Lunch is provided onsite, and the setting emphasizes safety, organization, and high-quality laboratory practices.Job Type &amp; LocationThis is a Contract to Hire position based out of South San Francisco, CA.Pay and BenefitsThe pay range for this position is $28.00 - $32.00/hr.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 South San Francisco,CA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Associate

Job Title: Lab CQV SpecialistJob DescriptionThe QC Laboratory Equipment Qualification &amp; Validation Specialist manages the full lifecycle of quality control laboratory equipment in a GMP-regulated pharmaceutical environment. This role leads the installation, commissioning, qualification, decommissioning, and re-commissioning of analytical and support equipment, ensuring that all instruments and systems remain qualified, maintained, and compliant with regulatory requirements, internal procedures, and data integrity standards. The specialist works closely with cross-functional teams to support laboratory readiness, inspection preparedness, and continuous improvement across both new and existing QC laboratories.Responsibilities<ul><li>Lead and execute installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities for QC laboratory equipment in accordance with approved protocols and regulatory expectations.</li><li>Develop, review, and approve qualification documentation, including validation plans, risk assessments, protocols, and final reports for QC instruments and systems.</li><li>Perform commissioning and decommissioning activities for laboratory instruments, ensuring proper documentation, adherence to change control processes, and alignment with lifecycle management strategies.</li><li>Support re-qualification and periodic review of existing laboratory equipment to maintain a validated state throughout its lifecycle.</li><li>Coordinate and support the installation, relocation, and startup of new and existing QC laboratory equipment, including planning and oversight of on-site activities.</li><li>Manage equipment lifecycle events such as upgrades, replacements, retirements, and obsolescence planning to ensure continuity of laboratory operations.</li><li>Interface with external vendors during factory acceptance testing (FAT), site acceptance testing (SAT), installation, qualification, and service activities.</li><li>Provide qualification and validation support for analytical instruments including HPLC/UPLC systems, balances, pH meters, spectroscopic systems, and dissolution equipment.</li><li>Support qualification and validation of laboratory utilities and systems such as purified water and WFI systems, water testing equipment, and environmental monitoring systems.</li><li>Qualify and maintain particle counters, temperature-controlled units (incubators, ovens, refrigerators, freezers), and other critical QC laboratory equipment.</li><li>Ensure all qualification, validation, and lifecycle activities comply with cGMP, FDA, ICH, USP, EU Annex 11, and applicable data integrity requirements.</li><li>Initiate and support deviations, investigations, corrective and preventive actions (CAPAs), and change controls related to laboratory equipment and systems.</li><li>Author, review, and revise standard operating procedures (SOPs), work instructions, and validation templates that govern equipment management and qualification processes.</li><li>Maintain audit-ready documentation and actively support internal, client, and regulatory inspections by providing technical and documentation support.</li><li>Partner with QC analysts, QA, Engineering, Metrology, and IT to ensure successful equipment qualification, ongoing compliance, and timely resolution of issues.</li><li>Provide technical guidance and training to QC laboratory staff on equipment use, qualification status, and documentation expectations.</li><li>Support laboratory expansions, technology transfers, and continuous improvement initiatives by providing CQV expertise and project support.</li><li>Act as a project lead or project manager for new lab validation and systems validation, identifying gaps, developing remediation plans, and driving execution to close gaps.</li><li>Contribute to the establishment and validation of a brand new microbiology laboratory while also supporting four existing laboratories on site.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Chemistry, Biology, Engineering, or a related scientific discipline, or equivalent experience.</li><li>3–7+ years of experience in commissioning, qualification, and validation (CQV), equipment qualification, or validation within a pharmaceutical, biotechnology, or regulated laboratory environment.</li><li>Demonstrated experience qualifying QC laboratory equipment, including analytical instruments and laboratory systems, in a GMP environment.</li><li>Hands-on experience with IQ/OQ/PQ execution and documentation for laboratory instruments and utilities.</li><li>Installation Qualification experience, with a minimum of 5–8 years installing and qualifying new laboratory equipment such as HPLC systems, balances, water systems, and particle counters.</li><li>Strong understanding of cGMP regulations, data integrity principles, and regulatory expectations for laboratory equipment and computerized systems.</li><li>Experience with change control systems, deviation management, and CAPA processes in a regulated environment.</li><li>Familiarity with electronic systems such as LIMS, CMMS, validation management systems, and document management systems.</li><li>Experience with computer systems validation (CSV) for laboratory-related systems.</li><li>Excellent technical writing skills for authoring and reviewing validation protocols, reports, and SOPs.</li><li>Strong organizational skills with the ability to manage multiple concurrent qualification and validation activities.</li><li>Effective communication skills to collaborate with cross-functional teams and provide clear technical guidance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience supporting QC laboratories in a commercial or late-stage manufacturing environment.</li><li>Familiarity with ASTM E2500 and risk-based validation approaches for equipment and systems qualification.</li><li>Experience supporting regulatory inspections, including FDA, EMA, and MHRA inspections.</li><li>Prior experience with laboratory expansions, new facility start-ups, or major equipment upgrade projects.</li><li>Experience validating new laboratories and associated systems, including utilities and monitoring systems.</li><li>Ability to work independently, identify gaps in equipment and systems compliance, and drive corrective actions to completion.</li><li>Strong problem-solving skills and a continuous improvement mindset to enhance equipment qualification and lifecycle processes.</li></ul>Work EnvironmentThis is an on-site role based in a GMP-controlled laboratory environment operating during normal business hours. The position supports multiple QC laboratories, including a brand new microbiology lab and several existing labs on site. The work takes place in regulated lab spaces that operate under DEA and GMP controls, with extensive use of analytical instruments, laboratory utilities, and computerized systems. The role is highly independent in nature, with responsibilities similar to a project manager who assesses gaps in equipment qualification and compliance and leads efforts to resolve them. Collaboration with QC, QA, Engineering, Metrology, IT, and external vendors is frequent, and the environment emphasizes inspection readiness, documentation accuracy, and adherence to established procedures.Job Type &amp; LocationThis is a Contract position based out of Wilson, NC.Pay and BenefitsThe pay range for this position is $50.00 - $62.00/hr.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 Wilson,NC.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab CQV Specialist

Job Title: Lab Operations SpecialistLocation/Shift: <ul><li>Cambridge, MA - Tuesday - Saturday - 8am - 4:30pm</li></ul>Job DescriptionThe Lab Operations Specialist supports end-to-end sample management and laboratory operations across multiple departments in a regulated environment. This role follows SOPs and GMP procedures, ensures accurate documentation in ERP and quality systems, and assists with biopsy accessioning and cleanroom activities to maintain high standards of quality and compliance.Responsibilities<ul><li>Support sample management activities across several laboratory and operational departments in alignment with SOPs and GMP procedures.</li><li>Move and coordinate materials across all departments to ensure timely and accurate processing of samples and supplies.</li><li>Ensure all samples are accurately documented in ERP and quality systems, including maintaining detailed records in Excel.</li><li>Perform biopsy accessioning activities for all relevant processes, ensuring correct identification, labeling, and tracking of samples.</li><li>Assist with gowning procedures and related activities in the cleanroom to maintain a controlled and compliant environment.</li><li>Support media preparation and inventory management to ensure laboratory materials are adequately stocked and organized.</li><li>Carry out data entry and Excel data entry tasks with a high level of accuracy and attention to detail.</li><li>Follow cGMP, GMP, SOP, and other operational guidelines to maintain compliance with regulatory and quality standards.</li><li>Participate in general laboratory operations, including receiving and accessioning samples, and maintaining orderly workspaces.</li><li>Collaborate with cross-functional teams to support efficient lab operations and continuous improvement of sample management processes.</li></ul>Essential Skills<ul><li>2–4 years of experience in laboratory operations, sample management, or a closely related field.</li><li>Associate degree in a relevant discipline.</li><li>Hands-on experience with sample management, including receiving, tracking, and accessioning samples.</li><li>Proficiency in Excel, including accurate data entry and basic data organization.</li><li>Experience with media preparation and inventory management in a laboratory setting.</li><li>Working knowledge of ERP systems and quality systems for documenting and tracking samples and materials.</li><li>Demonstrated ability to follow SOPs, GMP, and cGMP procedures in a regulated environment.</li><li>Strong attention to detail and accuracy in data entry and documentation.</li><li>Ability to work effectively across multiple departments and support various operational workflows.</li><li>Comfort with laboratory operations, including handling biological samples and working in cleanroom environments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with laboratory accessioning and receiving processes.</li><li>Familiarity with general laboratory operations and sample management best practices.</li><li>Ability to learn and apply evolving GMP requirements and operational procedures.</li><li>Strong organizational skills and the ability to manage multiple tasks in a fast-paced environment.</li><li>Interest in long-term growth opportunities, including potential promotion and expanded responsibilities.</li><li>Motivation to work in a quality-focused environment with structured procedures and documentation.</li></ul>Work EnvironmentThe role follows a consistent schedule from Tuesday to Saturday, 8:00 a.m. to 4:30 p.m., providing stable working hours with weekend coverage. The position is based in a laboratory environment that includes cleanroom operations, where proper gowning procedures are required to maintain controlled conditions. You will work across various departments, gaining exposure to GMP practices, ERP and quality systems, and media preparation and inventory processes. The environment emphasizes regulatory compliance, accurate documentation, and collaboration. As the role progresses, there is potential for promotion and transition to a full-time position with access to comprehensive benefits, restricted stock units, and bonuses, reflecting a culture that values development, performance, and long-term career growth.Job Type &amp; LocationThis is a Contract to Hire position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $20.00 - $24.00/hr.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 Aug 4, 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.

Lab Operations Coordinator

Job Title: Lab Operations SpecialistLocation/Shift: <ul><li>Cambridge, MA - Tuesday - Saturday - 8am - 4:30pm</li></ul>Job DescriptionThe Lab Operations Specialist supports end-to-end sample management and laboratory operations across multiple departments in a regulated environment. This role follows SOPs and GMP procedures, ensures accurate documentation in ERP and quality systems, and assists with biopsy accessioning and cleanroom activities to maintain high standards of quality and compliance.Responsibilities<ul><li>Support sample management activities across several laboratory and operational departments in alignment with SOPs and GMP procedures.</li><li>Move and coordinate materials across all departments to ensure timely and accurate processing of samples and supplies.</li><li>Ensure all samples are accurately documented in ERP and quality systems, including maintaining detailed records in Excel.</li><li>Perform biopsy accessioning activities for all relevant processes, ensuring correct identification, labeling, and tracking of samples.</li><li>Assist with gowning procedures and related activities in the cleanroom to maintain a controlled and compliant environment.</li><li>Support media preparation and inventory management to ensure laboratory materials are adequately stocked and organized.</li><li>Carry out data entry and Excel data entry tasks with a high level of accuracy and attention to detail.</li><li>Follow cGMP, GMP, SOP, and other operational guidelines to maintain compliance with regulatory and quality standards.</li><li>Participate in general laboratory operations, including receiving and accessioning samples, and maintaining orderly workspaces.</li><li>Collaborate with cross-functional teams to support efficient lab operations and continuous improvement of sample management processes.</li></ul>Essential Skills<ul><li>2–4 years of experience in laboratory operations, sample management, or a closely related field.</li><li>Associate degree in a relevant discipline.</li><li>Hands-on experience with sample management, including receiving, tracking, and accessioning samples.</li><li>Proficiency in Excel, including accurate data entry and basic data organization.</li><li>Experience with media preparation and inventory management in a laboratory setting.</li><li>Working knowledge of ERP systems and quality systems for documenting and tracking samples and materials.</li><li>Demonstrated ability to follow SOPs, GMP, and cGMP procedures in a regulated environment.</li><li>Strong attention to detail and accuracy in data entry and documentation.</li><li>Ability to work effectively across multiple departments and support various operational workflows.</li><li>Comfort with laboratory operations, including handling biological samples and working in cleanroom environments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with laboratory accessioning and receiving processes.</li><li>Familiarity with general laboratory operations and sample management best practices.</li><li>Ability to learn and apply evolving GMP requirements and operational procedures.</li><li>Strong organizational skills and the ability to manage multiple tasks in a fast-paced environment.</li><li>Interest in long-term growth opportunities, including potential promotion and expanded responsibilities.</li><li>Motivation to work in a quality-focused environment with structured procedures and documentation.</li></ul>Work EnvironmentThe role follows a consistent schedule from Tuesday to Saturday, 8:00 a.m. to 4:30 p.m., providing stable working hours with weekend coverage. The position is based in a laboratory environment that includes cleanroom operations, where proper gowning procedures are required to maintain controlled conditions. You will work across various departments, gaining exposure to GMP practices, ERP and quality systems, and media preparation and inventory processes. The environment emphasizes regulatory compliance, accurate documentation, and collaboration. As the role progresses, there is potential for promotion and transition to a full-time position with access to comprehensive benefits, restricted stock units, and bonuses, reflecting a culture that values development, performance, and long-term career growth.Job Type &amp; LocationThis is a Contract to Hire position based out of Cambridge, MA.Pay and BenefitsThe pay range for this position is $20.00 - $24.00/hr.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 Jul 31, 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: Lab Operations SpecialistJob DescriptionThe Lab Operations Specialist serves as a key liaison between internal and external stakeholders to manage inventory activities and provide accurate, efficient laboratory support. This role oversees the movement, storage, control, and protection of raw materials, supplies, work-in-process products, and finished goods. The specialist ensures materials and finished products are handled in accordance with established processes and procedures while supporting continuous improvement across lab and manufacturing operations.Responsibilities<ul><li>Work closely with cross-functional teams, including Manufacturing Operations, Donor Centers, and Quality Assurance, to receive, inspect, release, store, monitor, and issue materials internally and ship finished goods to customers.</li><li>Ensure final disposition of materials and finished goods follows established processes, procedures, and documentation requirements.</li><li>Schedule and perform cycle count activities, ensuring counts are completed accurately and on time.</li><li>Investigate and troubleshoot inventory discrepancies identified during cycle counts and update designated metric reports with findings and resolutions.</li><li>Monitor storage space availability within assigned areas and recommend improvements to optimize space utilization.</li><li>Participate in the review, development, and updating of material handling Standard Operating Procedures (SOPs) and related company guidelines.</li><li>Assist in the development, tracking, and maintenance of Manufacturing Operations metrics, including inventory and material handling performance indicators.</li><li>Support training of existing and new employees in material handling processes and assist with recruitment activities for new material handlers as requested.</li><li>Comply with company policies and adhere to all safety requirements when handling materials or working in designated areas.</li><li>Ensure equipment used for material handling and lab operations is maintained to high operational standards and promptly report any discrepancies or malfunctions to management.</li><li>Support management in continuous improvement initiatives aimed at optimizing efficiency and effectiveness of material handling operations.</li><li>Participate in special projects and perform other related duties as required by operational needs.</li><li>Perform responsibilities using appropriate Personal Protective Equipment (PPE) when required and promote safe work practices.</li><li>Perform material handling activities including shipping and receiving functions such as inspection, tagging, packaging of materials, discarding boxes appropriately, and maintaining the shipping area in an orderly condition.</li><li>Pick, pull, and package materials prior to internal issuance and/or off-site shipping, ensuring accuracy and traceability.</li><li>Handle finished goods materials under cryo-frozen conditions in accordance with established procedures and safety guidelines.</li><li>Apply basic inventory management principles, including First-In-First-Out (FIFO) and Kanban systems, to maintain accurate inventory levels and flow.</li><li>Perform quality control inspections for incoming raw materials in line with applicable procedures and document results accurately.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in lab management.</li><li>Hands-on experience in lab operations and working with lab equipment.</li><li>Strong understanding of Good Manufacturing Practices (GMP).</li><li>Experience with electronic and paper-based inventory control systems.</li><li>Strong understanding of ERP systems and inventory transactions.</li><li>Ability to write clear, accurate Standard Operating Procedures (SOPs).</li><li>Strong computer skills, including proficiency in Excel.</li><li>Physical ability to move moderately heavy and/or bulky materials.</li><li>Ability to work safely with cryo-frozen materials and follow detailed procedures.</li><li>Capability to investigate and resolve inventory discrepancies with attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with handling cryo-frozen materials is an asset.</li><li>Experience with both electronic and paper-based inventory control systems is an asset.</li><li>Knowledge of quality standards such as ISO 9001 is desired.</li><li>Working knowledge of creating pivot tables in Excel is an asset.</li><li>Familiarity with inventory management approaches such as FIFO and Kanban.</li><li>Ability to contribute to continuous improvement initiatives in material handling and lab operations.</li><li>Comfort working in cross-functional environments with Manufacturing, Donor Centers, and Quality Assurance.</li><li>Strong communication skills to support training and collaboration with internal and external stakeholders.</li></ul>Work EnvironmentThis position is fully onsite in Emeryville and supports laboratory and manufacturing operations focused on collecting and processing donated blood and bone marrow specimens into research-ready samples. The work schedule follows a Monday through Friday pattern with flexible working hours to accommodate operational needs. The environment involves frequent interaction with lab equipment, inventory management systems, ERP platforms, and electronic and paper-based documentation. The role includes regular handling of raw materials, supplies, and finished goods, including work under cryo-frozen conditions. Personal Protective Equipment (PPE) is used as required, and the facility follows established safety procedures and Good Manufacturing Practices. The setting emphasizes collaboration, accuracy, and efficiency to increase access to biologically relevant samples and support research worldwide.Job Type &amp; LocationThis is a Contract to Hire position based out of Emeryville, CA.Pay and BenefitsThe pay range for this position is $35.00 - $38.00/hr.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 Emeryville,CA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Operations Specialist

Job Title: Lab Operations SpecialistJob DescriptionThe Lab Operations Specialist serves as a key liaison between internal and external stakeholders for all inventory-related activities within the laboratory. This role provides accurate and efficient operational support for the movement, storage, control, and protection of raw materials, supplies, work-in-process products, and finished goods. The specialist helps ensure that materials are handled in compliance with established procedures and quality standards, enabling reliable and timely support for research and manufacturing operations.Responsibilities<ul><li>Work closely with cross-functional teams, including Manufacturing Operations, Donor Center, and Quality Assurance, to receive, inspect, release, store, monitor, and issue materials internally, as well as ship finished goods to customers.</li><li>Ensure final disposition of materials and finished goods follows established processes, procedures, and quality requirements.</li><li>Schedule and perform inventory cycle counts, ensuring all counts are completed accurately and on time.</li><li>Investigate and troubleshoot inventory discrepancies identified during cycle counts and update designated metric reports accordingly.</li><li>Monitor storage space availability within assigned areas and recommend improvements to optimize space utilization.</li><li>Participate in reviewing and updating material handling Standard Operating Procedures (SOPs) and company guidelines.</li><li>Assist in the development and maintenance of Manufacturing Operations metrics to track performance and efficiency.</li><li>Support training activities for existing and new employees and assist with recruitment efforts for new material handlers as requested.</li><li>Comply with company policies and adhere to all safety requirements when handling materials or working in designated areas.</li><li>Ensure equipment is maintained to high operational standards and promptly report any discrepancies or issues to management.</li><li>Support management in continuous improvement initiatives aimed at optimizing and increasing the efficiency of material handling operations.</li><li>Participate in special projects and perform other related duties as assigned.</li><li>Perform responsibilities while wearing appropriate Personal Protective Equipment (PPE) when required.</li><li>Proactively execute material handling activities, including shipping and receiving functions such as inspection, tagging, packaging of materials, discarding boxes appropriately, and maintaining the shipping area in an organized condition.</li><li>Pick, pull, and package materials for internal issuance and off-site shipping in accordance with established procedures.</li><li>Handle finished goods materials under cryo-frozen conditions following applicable procedures and safety guidelines.</li><li>Apply basic inventory management principles, including First-In-First-Out (FIFO) and Kanban methodologies, to ensure proper stock rotation and availability.</li><li>Perform quality control inspections for incoming raw materials in alignment with applicable procedures and quality standards.</li><li>Support the use and accuracy of electronic and paper-based inventory control systems and contribute to maintaining reliable inventory records.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in lab management.</li><li>Hands-on experience with lab operations and lab equipment.</li><li>Knowledge and practical application of Good Manufacturing Practices (GMP).</li><li>Strong understanding of ERP systems and inventory transactions.</li><li>Ability to write clear and accurate Standard Operating Procedures (SOPs).</li><li>Strong computer skills, including proficiency with Microsoft Excel.</li><li>Physical ability to move moderately heavy and bulky materials safely.</li><li>Ability to work effectively with cross-functional teams and multiple stakeholders.</li><li>Strong attention to detail and accuracy in inventory control and documentation.</li><li>Commitment to following safety requirements and using PPE as required.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with electronic and paper-based inventory control systems.</li><li>Experience handling cryo-frozen materials.</li><li>Knowledge of quality standards such as ISO 9001.</li><li>Working knowledge of creating pivot tables in Microsoft Excel.</li><li>Familiarity with basic inventory management systems, including FIFO and Kanban.</li><li>Experience performing quality control inspections for incoming raw materials.</li><li>Experience participating in continuous improvement initiatives within operations or logistics environments.</li></ul>Work EnvironmentThis role is based onsite in Emeryville and supports a laboratory environment that collects and processes donated blood and bone marrow specimens into samples used by researchers worldwide. The position follows a Monday through Friday schedule with flexible working hours, supporting both manufacturing and research-focused operations. Work is performed in a lab and warehouse setting that involves handling raw materials, supplies, and cryo-frozen finished goods, with regular use of lab equipment and inventory management systems. The role requires consistent adherence to safety protocols, including the use of Personal Protective Equipment (PPE) when handling materials or working in designated areas, and the physical ability to move moderately heavy and bulky materials. The environment emphasizes quality, operational efficiency, and continuous improvement, providing an opportunity to contribute directly to advancing scientific research through reliable and well-managed lab operations.Job Type &amp; LocationThis is a Contract to Hire position based out of Emeryville, CA.Pay and BenefitsThe pay range for this position is $35.00 - $38.00/hr.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 Emeryville,CA.Application DeadlineThis position is anticipated to close on Jul 31, 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: Lab Operations SpecialistJob DescriptionThe Lab Operations Specialist serves as a key liaison between internal and external stakeholders for all inventory-related activities within the laboratory. This role provides accurate and efficient operational support for the movement, storage, control, and protection of raw materials, supplies, work-in-process products, and finished goods. The specialist helps ensure that materials are handled in compliance with established procedures and quality standards, enabling reliable and timely support for research and manufacturing operations.Responsibilities<ul><li>Work closely with cross-functional teams, including Manufacturing Operations, Donor Center, and Quality Assurance, to receive, inspect, release, store, monitor, and issue materials internally, as well as ship finished goods to customers.</li><li>Ensure final disposition of materials and finished goods follows established processes, procedures, and quality requirements.</li><li>Schedule and perform inventory cycle counts, ensuring all counts are completed accurately and on time.</li><li>Investigate and troubleshoot inventory discrepancies identified during cycle counts and update designated metric reports accordingly.</li><li>Monitor storage space availability within assigned areas and recommend improvements to optimize space utilization.</li><li>Participate in reviewing and updating material handling Standard Operating Procedures (SOPs) and company guidelines.</li><li>Assist in the development and maintenance of Manufacturing Operations metrics to track performance and efficiency.</li><li>Support training activities for existing and new employees and assist with recruitment efforts for new material handlers as requested.</li><li>Comply with company policies and adhere to all safety requirements when handling materials or working in designated areas.</li><li>Ensure equipment is maintained to high operational standards and promptly report any discrepancies or issues to management.</li><li>Support management in continuous improvement initiatives aimed at optimizing and increasing the efficiency of material handling operations.</li><li>Participate in special projects and perform other related duties as assigned.</li><li>Perform responsibilities while wearing appropriate Personal Protective Equipment (PPE) when required.</li><li>Proactively execute material handling activities, including shipping and receiving functions such as inspection, tagging, packaging of materials, discarding boxes appropriately, and maintaining the shipping area in an organized condition.</li><li>Pick, pull, and package materials for internal issuance and off-site shipping in accordance with established procedures.</li><li>Handle finished goods materials under cryo-frozen conditions following applicable procedures and safety guidelines.</li><li>Apply basic inventory management principles, including First-In-First-Out (FIFO) and Kanban methodologies, to ensure proper stock rotation and availability.</li><li>Perform quality control inspections for incoming raw materials in alignment with applicable procedures and quality standards.</li><li>Support the use and accuracy of electronic and paper-based inventory control systems and contribute to maintaining reliable inventory records.</li></ul>Essential Skills<ul><li>Minimum of 5 years of experience in lab management.</li><li>Hands-on experience with lab operations and lab equipment.</li><li>Knowledge and practical application of Good Manufacturing Practices (GMP).</li><li>Strong understanding of ERP systems and inventory transactions.</li><li>Ability to write clear and accurate Standard Operating Procedures (SOPs).</li><li>Strong computer skills, including proficiency with Microsoft Excel.</li><li>Physical ability to move moderately heavy and bulky materials safely.</li><li>Ability to work effectively with cross-functional teams and multiple stakeholders.</li><li>Strong attention to detail and accuracy in inventory control and documentation.</li><li>Commitment to following safety requirements and using PPE as required.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with electronic and paper-based inventory control systems.</li><li>Experience handling cryo-frozen materials.</li><li>Knowledge of quality standards such as ISO 9001.</li><li>Working knowledge of creating pivot tables in Microsoft Excel.</li><li>Familiarity with basic inventory management systems, including FIFO and Kanban.</li><li>Experience performing quality control inspections for incoming raw materials.</li><li>Experience participating in continuous improvement initiatives within operations or logistics environments.</li></ul>Work EnvironmentThis role is based onsite in Emeryville and supports a laboratory environment that collects and processes donated blood and bone marrow specimens into samples used by researchers worldwide. The position follows a Monday through Friday schedule with flexible working hours, supporting both manufacturing and research-focused operations. Work is performed in a lab and warehouse setting that involves handling raw materials, supplies, and cryo-frozen finished goods, with regular use of lab equipment and inventory management systems. The role requires consistent adherence to safety protocols, including the use of Personal Protective Equipment (PPE) when handling materials or working in designated areas, and the physical ability to move moderately heavy and bulky materials. The environment emphasizes quality, operational efficiency, and continuous improvement, providing an opportunity to contribute directly to advancing scientific research through reliable and well-managed lab operations.Job Type &amp; LocationThis is a Contract to Hire position based out of Emeryville, CA.Pay and BenefitsThe pay range for this position is $35.00 - $38.00/hr.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 Emeryville,CA.Application DeadlineThis position is anticipated to close on Aug 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.

Job Title: Lab Research Analyst IJob DescriptionThe Lab Research Analyst I is a hands-on laboratory scientist who supports the development of new vaccines and therapeutics by studying immune responses. This role focuses on receiving and processing samples from preclinical and clinical studies, performing complex immunology and molecular biology experiments, and generating high-quality data that informs vaccine research. The position requires meticulous bench work, consistent execution of detailed protocols, and close collaboration with scientists and laboratory leadership in a fast-paced, mission-driven research environment.Responsibilities<ul><li>Receive and process human, macaque, and mouse samples from vaccine studies and clinical trials, ensuring careful handling and accurate tracking of all specimens.</li><li>Isolate, enrich, culture, and sequence B cells to evaluate antibody responses following immunization.</li><li>Perform cell culture work, including establishing and maintaining primary cell cultures under defined conditions.</li><li>Conduct molecular biology techniques such as nucleic acid extraction, RNA extraction, RT-PCR, PCR, qPCR, and related workflows to support immunology and vaccine research.</li><li>Prepare samples for next-generation sequencing (NGS), following established protocols to preserve sample quality and integrity.</li><li>Execute single-cell B-cell isolation and antibody gene sequencing workflows involving thousands of individual cell samples with a high degree of precision.</li><li>Run immunological assays, including ELISA, bead-based immunoassays, immunofluorescence staining, and microscopy-based analyses to characterize immune responses.</li><li>Utilize flow cytometry for cell sorting and analysis and contribute to data interpretation using tools such as FlowJo and GraphPad Prism where applicable.</li><li>Support recombinant antibody production, purification, and quality control activities to generate high-quality reagents for research studies.</li><li>Maintain detailed, accurate experimental documentation and electronic records, ensuring all work complies with standard operating procedures (SOPs) and laboratory quality standards.</li><li>Collaborate closely with scientists, laboratory leadership, and support staff to achieve project milestones and meet regulatory and FDA-related timelines.</li><li>Assist with general laboratory operations, including equipment upkeep, routine maintenance, reagent preparation, inventory control, and supply tracking.</li><li>Follow rigorous contamination-control practices and execute repetitive, highly detailed laboratory workflows consistently to maintain data integrity.</li><li>Work effectively with advanced robotics and sequencing equipment by adhering to established workflows and contributing to continuous process improvements.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biology, Immunology, Molecular Biology, Biochemistry, Zoology, Botany, Psychology, or a closely related scientific discipline.</li><li>Minimum of 2 years of laboratory research experience; a Master’s degree may substitute for this experience.</li><li>Hands-on experience with cell culture and primary cell culture techniques.</li><li>Proficiency in nucleic acid extraction, including RNA extraction.</li><li>Practical experience performing RT-PCR, PCR, qPCR, and related molecular biology techniques.</li><li>Experience running ELISA and/or bead-based immunoassays.</li><li>Demonstrated ability to maintain detailed laboratory documentation and adhere to SOPs and quality standards.</li><li>Strong foundation in immunology, vaccine, molecular biology, or antibody-focused laboratory environments.</li><li>Proficiency in handling fragile biological samples and executing highly detailed, repetitive bench protocols with precision.</li><li>High level of attention to detail, accuracy, and consistency in experimental execution and data recording.</li><li>Comfort working with complex, multi-step workflows and maintaining sample integrity throughout the process.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with single-cell PCR and antibody sequencing workflows.</li><li>Experience preparing samples for next-generation sequencing (NGS).</li><li>Flow cytometry experience, including cell sorting and data analysis using FlowJo.</li><li>Experience with antibody repertoire analysis or immune profiling research.</li><li>Exposure to vaccine, immunology, infectious disease, or antibody discovery research programs.</li><li>Mouse handling and in vivo research experience.</li><li>Familiarity with GraphPad Prism for data analysis and visualization.</li><li>Interest in working in a mission-driven environment focused on next-generation vaccines and therapeutics.</li><li>Ability to thrive in a fast-paced, collaborative research setting with high expectations for scientific rigor and data quality.</li><li>Motivation to develop professionally through structured training, certifications, and exposure to sophisticated research systems.</li></ul>Work EnvironmentThis position is fully onsite within a high-volume laboratory environment that supports large-scale, complex vaccine and immunology research programs. The lab operates advanced robotics, high-throughput sequencing platforms, and modern instrumentation for cell culture, molecular biology, flow cytometry, and immunoassays. Work involves extended periods at the bench performing detailed, repetitive workflows where precision and contamination control are critical. Team members collaborate closely with faculty, scientists, and research staff in a fast-paced, high-performing culture that values communication, shared problem-solving, and scientific excellence. The organization offers a world-class research setting with substantial research funding, multi-institutional collaborations, and opportunities for growth, learning, and professional development in research administration, federal compliance, and sponsored project management.Job Type &amp; LocationThis is a Contract position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $25.23 - $31.73/hr.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 Raleigh,NC.Application DeadlineThis position is anticipated to close on Aug 7, 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.

Lab Research Analyst

Job Title: Lab Research Analyst IJob DescriptionThe Lab Research Analyst I is a hands-on laboratory scientist who supports the development of new vaccines and therapeutics by studying immune responses. This role focuses on receiving and processing samples from preclinical and clinical studies, performing complex immunology and molecular biology experiments, and generating high-quality data that informs vaccine research. The position requires meticulous bench work, consistent execution of detailed protocols, and close collaboration with scientists and laboratory leadership in a fast-paced, mission-driven research environment.Responsibilities<ul><li>Receive and process human, macaque, and mouse samples from vaccine studies and clinical trials, ensuring careful handling and accurate tracking of all specimens.</li><li>Isolate, enrich, culture, and sequence B cells to evaluate antibody responses following immunization.</li><li>Perform cell culture work, including establishing and maintaining primary cell cultures under defined conditions.</li><li>Conduct molecular biology techniques such as nucleic acid extraction, RNA extraction, RT-PCR, PCR, qPCR, and related workflows to support immunology and vaccine research.</li><li>Prepare samples for next-generation sequencing (NGS), following established protocols to preserve sample quality and integrity.</li><li>Execute single-cell B-cell isolation and antibody gene sequencing workflows involving thousands of individual cell samples with a high degree of precision.</li><li>Run immunological assays, including ELISA, bead-based immunoassays, immunofluorescence staining, and microscopy-based analyses to characterize immune responses.</li><li>Utilize flow cytometry for cell sorting and analysis and contribute to data interpretation using tools such as FlowJo and GraphPad Prism where applicable.</li><li>Support recombinant antibody production, purification, and quality control activities to generate high-quality reagents for research studies.</li><li>Maintain detailed, accurate experimental documentation and electronic records, ensuring all work complies with standard operating procedures (SOPs) and laboratory quality standards.</li><li>Collaborate closely with scientists, laboratory leadership, and support staff to achieve project milestones and meet regulatory and FDA-related timelines.</li><li>Assist with general laboratory operations, including equipment upkeep, routine maintenance, reagent preparation, inventory control, and supply tracking.</li><li>Follow rigorous contamination-control practices and execute repetitive, highly detailed laboratory workflows consistently to maintain data integrity.</li><li>Work effectively with advanced robotics and sequencing equipment by adhering to established workflows and contributing to continuous process improvements.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Biology, Immunology, Molecular Biology, Biochemistry, Zoology, Botany, Psychology, or a closely related scientific discipline.</li><li>Minimum of 2 years of laboratory research experience; a Master’s degree may substitute for this experience.</li><li>Hands-on experience with cell culture and primary cell culture techniques.</li><li>Proficiency in nucleic acid extraction, including RNA extraction.</li><li>Practical experience performing RT-PCR, PCR, qPCR, and related molecular biology techniques.</li><li>Experience running ELISA and/or bead-based immunoassays.</li><li>Demonstrated ability to maintain detailed laboratory documentation and adhere to SOPs and quality standards.</li><li>Strong foundation in immunology, vaccine, molecular biology, or antibody-focused laboratory environments.</li><li>Proficiency in handling fragile biological samples and executing highly detailed, repetitive bench protocols with precision.</li><li>High level of attention to detail, accuracy, and consistency in experimental execution and data recording.</li><li>Comfort working with complex, multi-step workflows and maintaining sample integrity throughout the process.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with single-cell PCR and antibody sequencing workflows.</li><li>Experience preparing samples for next-generation sequencing (NGS).</li><li>Flow cytometry experience, including cell sorting and data analysis using FlowJo.</li><li>Experience with antibody repertoire analysis or immune profiling research.</li><li>Exposure to vaccine, immunology, infectious disease, or antibody discovery research programs.</li><li>Mouse handling and in vivo research experience.</li><li>Familiarity with GraphPad Prism for data analysis and visualization.</li><li>Interest in working in a mission-driven environment focused on next-generation vaccines and therapeutics.</li><li>Ability to thrive in a fast-paced, collaborative research setting with high expectations for scientific rigor and data quality.</li><li>Motivation to develop professionally through structured training, certifications, and exposure to sophisticated research systems.</li></ul>Work EnvironmentThis position is fully onsite within a high-volume laboratory environment that supports large-scale, complex vaccine and immunology research programs. The lab operates advanced robotics, high-throughput sequencing platforms, and modern instrumentation for cell culture, molecular biology, flow cytometry, and immunoassays. Work involves extended periods at the bench performing detailed, repetitive workflows where precision and contamination control are critical. Team members collaborate closely with faculty, scientists, and research staff in a fast-paced, high-performing culture that values communication, shared problem-solving, and scientific excellence. The organization offers a world-class research setting with substantial research funding, multi-institutional collaborations, and opportunities for growth, learning, and professional development in research administration, federal compliance, and sponsored project management.Job Type &amp; LocationThis is a Contract position based out of Raleigh, NC.Pay and BenefitsThe pay range for this position is $25.23 - $31.73/hr.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 Raleigh,NC.Application DeadlineThis position is anticipated to close on Aug 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.

Job Title: Lead Lab TechnicianJob DescriptionWe are seeking a meticulous and skilled Lead Lab Technician to join our team. The role involves performing microbiological testing and analysis of food, beverage, and environmental samples using advanced technologies such as qPCR and ELFA. You will be responsible for maintaining data accuracy and ensuring compliance with safety protocols in a dynamic laboratory environment.Responsibilities<ul><li>Receive, log, and label incoming samples, ensuring compliance with chain-of-custody procedures.</li><li>Verify the integrity and storage conditions of samples upon arrival.</li><li>Perform qualitative and quantitative testing for pathogens and indicator organisms.</li><li>Assist in conducting shelf-life studies, challenge studies, and environmental monitoring analyses.</li><li>Prepare, dilute, and plate samples using standard ISO, BAM, USDA-FSIS, and FDA methods.</li><li>Record and verify lab data for accuracy before releasing client reports.</li><li>Communicate findings to staff and assist with client inquiries.</li><li>Follow laboratory safety protocols, including PPE use and biosafety level requirements.</li><li>Maintain a clean and organized workspace adhering to ISO quality management standards.</li><li>Operate and maintain general laboratory equipment, performing routine maintenance and troubleshooting.</li><li>Assist with proficiency testing and participate in internal training programs.</li><li>Support special projects, including new product testing.</li></ul>Essential Skills<ul><li>Proficiency in microbiological testing and aseptic techniques.</li><li>Strong knowledge of qPCR and ELFA technologies.</li><li>Experience with pipetting, titration, and sterile processing.</li><li>Ability to adapt to workflow changes.</li><li>Strong data entry skills with a focus on accuracy.</li></ul>Additional Skills &amp; Qualifications<ul><li>1-2 years of experience with a degree or 4-5 years without a degree.</li><li>Basic microbiology testing experience on food.</li><li>Understanding of microbiology skill sets.</li></ul>Work EnvironmentYou will work in a small microbiology testing lab, focusing on generating data from samples rather than manufacturing. The work environment is laid-back with fluctuating workflow depending on client demands. The position involves a rotating shift schedule from Monday to Friday, 8:30 am-4:30 pm, and Tuesday to Saturday, with an early finish on Saturdays.If you are interested please book a virtual meeting with me here: https://talentassistant.actalentservices.com/assistant/bookings/bgF9HVktJob Type &amp; LocationThis is a Contract to Hire position based out of Farmington, CT.Pay and BenefitsThe pay range for this position is $27.00 - $35.00/hr.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 Farmington,CT.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Supervisor

Job Title: Lead Lab TechnicianJob DescriptionWe are seeking a meticulous and skilled Lead Lab Technician to join our team. The role involves performing microbiological testing and analysis of food, beverage, and environmental samples using advanced technologies such as qPCR and ELFA. You will be responsible for maintaining data accuracy and ensuring compliance with safety protocols in a dynamic laboratory environment.Responsibilities<ul><li>Receive, log, and label incoming samples, ensuring compliance with chain-of-custody procedures.</li><li>Verify the integrity and storage conditions of samples upon arrival.</li><li>Perform qualitative and quantitative testing for pathogens and indicator organisms.</li><li>Assist in conducting shelf-life studies, challenge studies, and environmental monitoring analyses.</li><li>Prepare, dilute, and plate samples using standard ISO, BAM, USDA-FSIS, and FDA methods.</li><li>Record and verify lab data for accuracy before releasing client reports.</li><li>staff and assist with client inquiries.</li><li>Follow laboratory safety protocols, including PPE use and biosafety level requirements.</li><li>Maintain a clean and organized workspace adhering to ISO quality management standards.</li><li>Operate and maintain general laboratory equipment, performing routine maintenance and troubleshooting.</li><li>Assist with proficiency testing and participate in internal training programs.</li><li>Support special projects, including new product testing.</li></ul>Essential Skills<ul><li>Proficiency in microbiological testing and aseptic techniques.</li><li>Strong knowledge of qPCR and ELFA technologies.</li><li>Experience with pipetting, titration, and sterile processing.</li><li>Ability to adapt to workflow changes.</li><li>Strong data entry skills with a focus on accuracy.</li></ul>Additional Skills &amp; Qualifications<ul><li>1-2 years of experience with a degree or 4-5 years without a degree.</li><li>Basic microbiology testing experience on food.</li><li>Understanding of microbiology skill sets.</li></ul>Work EnvironmentYou will work in a small microbiology testing lab, focusing on generating data from samples rather than manufacturing. The work environment is laid-back with fluctuating workflow depending on client demands. The position involves a rotating shift schedule from Monday to Friday, 8:30 am-4:30 pm, and Tuesday to Saturday, with an early finish on Saturdays.Job Type &amp; LocationThis is a Contract to Hire position based out of Farmington, CT.Pay and BenefitsThe pay range for this position is $27.00 - $35.00/hr.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 Farmington,CT.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Clinical Laboratory TechnologistEntry-level | #1 Hospital Worldwide | Excellent Room for Growth | Offers Benefits Job DescriptionThis position is within the Cell Kinetics LabPerform analyses on blood, tissue, and body fluids to aid healthcare providers in the diagnosis, prognosis, and treatment of patients. Testing is conducted in specialized laboratories and may involve highly skilled manual techniques or automated testing with sophisticated instrumentation.Responsibilities<ul><li>Operate and maintain laboratory instruments.</li><li>Troubleshoot assays and evaluate test accuracy.</li><li>Assist in interpreting results and provide operational support to optimize testing.</li><li>Work with multiple computer systems to retrieve information and report results.</li><li>Adhere to safety protocols while working with infectious specimens, chemicals, and other hazards.</li><li>Perform specimen collection as needed.</li><li>Process samples for leukemia and lymphoma testing, which includes pipetting, aliquotting, centrifuging, and adding chemicals to isolate white blood cells.</li><li>Stain white blood cells with antibodies and run stained cells on flow cytometers.</li></ul>Essential Skills<ul><li>Bachelor's degree in chemistry or a human biological science (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Animal Science, Marine Biology, Neuroscience).</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, MN.Pay and BenefitsThe pay range for this position is $23.00 - $24.00/hr.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 Rochester,MN.Application DeadlineThis position is anticipated to close on Aug 4, 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.

Lab Tech (Entry-level, #1 Hospital Worldwide)

Job Title: Lab Technician IIIJob DescriptionThe Bioanalytical group is seeking an experienced Lab Technician III / Bioanalytical Scientist to perform routine and non-routine analytical testing and formulation work in a GLP laboratory environment. This role focuses on bioanalytical and physical characterization of samples using techniques such as HPLC and spectroscopy, while generating reliable data to support project teams. The position is fully on-site, with the majority of time spent performing hands-on laboratory activities and the remainder dedicated to data documentation and collaboration.Responsibilities<ul><li>Perform routine and non-routine bioanalytical and physical testing, generating reliable and consistent results to support projects of varying complexity.</li><li>Work closely with project leads and technical team members to execute experimental plans and meet project objectives.</li><li>Conduct analyses using techniques such as HPLC and other bioanalytical methods, ensuring accurate data collection and interpretation.</li><li>Troubleshoot experiments and laboratory instrumentation to resolve issues and maintain data quality.</li><li>Carry out general laboratory maintenance and upkeep, including maintaining equipment, supplies, and a clean work area.</li><li>Perform routine testing and accurately document all experiments and results in electronic laboratory notebooks (eLN).</li><li>Learn, understand, and apply new experimental techniques and methods as needed for project work.</li><li>Follow and comply with all applicable standard operating procedures (SOPs), cGMP guidelines, GLP practices, and safety policies.</li><li>Maintain a clean, safe, and organized laboratory environment in accordance with internal procedures and regulatory expectations.</li><li>Collaborate and interface with multiple individuals from the technical team while working under the direction of a supervisor.</li><li>Support formulation work and visual evaluations, such as assessing color, clarity, and physical properties of samples, as required by project needs.</li></ul>Essential Skills<ul><li>Strong general science, with Chemistry or Biology preferred.</li><li>Proficiency in general laboratory skills, including pipetting, weighing, and solution preparation.</li><li>Hands-on experience with bioanalytical methods in a laboratory setting.</li><li>Practical experience with HPLC techniques and instrumentation.</li><li>Ability to use Empower or similar chromatography data systems for HPLC data acquisition and analysis.</li><li>Foundational knowledge in Biochemistry, Chemistry, Biology, Molecular Biology, or a related scientific discipline.</li><li>Theoretical and practical knowledge sufficient to independently carry out assigned laboratory functions.</li><li>Basic computer skills for data entry, documentation, and instrument-related software.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s or Master’s degree in Biochemistry, Chemistry, Biology, Molecular Biology, or a closely related scientific field.</li><li>Experience within a pharmaceutical or bioanalytical laboratory environment.</li><li>Familiarity or experience with particle sizing and particle testing techniques.</li><li>Exposure to force testing equipment and related analytical methods.</li><li>Experience with UV, IR, and fluorescence spectroscopy for sample characterization.</li><li>Understanding of basic practices for sampling, weighing, and pH measurement.</li><li>Ability to analyze and interpret bioanalytical data and communicate findings to project teams.</li><li>Comfort working in a GLP environment and following cGMP-related procedures.</li><li>Willingness to learn new techniques and adapt to evolving project requirements.</li></ul>Work EnvironmentThis position is 100% on-site in a GLP laboratory environment, with approximately 80% of time dedicated to hands-on lab activities and 20% to stationary tasks such as data analysis, documentation, and team collaboration. The role involves working directly with a supervisor while interfacing with multiple members of the technical team in a group-oriented setting. Standard hours are Monday through Friday, 8 hours per day. Work is performed in a regulated lab environment that emphasizes safety, cleanliness, and organization, with regular use of laboratory instruments such as HPLC systems, spectroscopy equipment, and particle testing tools. The assignment is initially planned for 12 months and may be extended based on performance and departmental needs.Job Type &amp; LocationThis is a Contract position based out of Waukegan, IL.Pay and BenefitsThe pay range for this position is $22.00 - $25.00/hr.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 Waukegan,IL.Application DeadlineThis position is anticipated to close on Jul 27, 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.

Lab Tech III

Job Title: Lab Technician IIIJob DescriptionThe Bioanalytical group is seeking an experienced Lab Technician III / Bioanalytical Scientist to perform routine and non-routine analytical testing and formulation work in a GLP laboratory environment. This role focuses on bioanalytical and physical characterization of samples using techniques such as HPLC and spectroscopy, while generating reliable data to support project teams. The position is fully on-site, with the majority of time spent performing hands-on laboratory activities and the remainder dedicated to data documentation and collaboration.Responsibilities<ul><li>Perform routine and non-routine bioanalytical and physical testing, generating reliable and consistent results to support projects of varying complexity.</li><li>Work closely with project leads and technical team members to execute experimental plans and meet project objectives.</li><li>Conduct analyses using techniques such as HPLC and other bioanalytical methods, ensuring accurate data collection and interpretation.</li><li>Troubleshoot experiments and laboratory instrumentation to resolve issues and maintain data quality.</li><li>Carry out general laboratory maintenance and upkeep, including maintaining equipment, supplies, and a clean work area.</li><li>Perform routine testing and accurately document all experiments and results in electronic laboratory notebooks (eLN).</li><li>Learn, understand, and apply new experimental techniques and methods as needed for project work.</li><li>Follow and comply with all applicable standard operating procedures (SOPs), cGMP guidelines, GLP practices, and safety policies.</li><li>Maintain a clean, safe, and organized laboratory environment in accordance with internal procedures and regulatory expectations.</li><li>Collaborate and interface with multiple individuals from the technical team while working under the direction of a supervisor.</li><li>Support formulation work and visual evaluations, such as assessing color, clarity, and physical properties of samples, as required by project needs.</li></ul>Essential Skills<ul><li>Strong general science, with Chemistry or Biology preferred.</li><li>Proficiency in general laboratory skills, including pipetting, weighing, and solution preparation.</li><li>Hands-on experience with bioanalytical methods in a laboratory setting.</li><li>Practical experience with HPLC techniques and instrumentation.</li><li>Ability to use Empower or similar chromatography data systems for HPLC data acquisition and analysis.</li><li>Foundational knowledge in Biochemistry, Chemistry, Biology, Molecular Biology, or a related scientific discipline.</li><li>Theoretical and practical knowledge sufficient to independently carry out assigned laboratory functions.</li><li>Basic computer skills for data entry, documentation, and instrument-related software.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s or Master’s degree in Biochemistry, Chemistry, Biology, Molecular Biology, or a closely related scientific field.</li><li>Experience within a pharmaceutical or bioanalytical laboratory environment.</li><li>Familiarity or experience with particle sizing and particle testing techniques.</li><li>Exposure to force testing equipment and related analytical methods.</li><li>Experience with UV, IR, and fluorescence spectroscopy for sample characterization.</li><li>Understanding of basic practices for sampling, weighing, and pH measurement.</li><li>Ability to analyze and interpret bioanalytical data and communicate findings to project teams.</li><li>Comfort working in a GLP environment and following cGMP-related procedures.</li><li>Willingness to learn new techniques and adapt to evolving project requirements.</li></ul>Work EnvironmentThis position is 100% on-site in a GLP laboratory environment, with approximately 80% of time dedicated to hands-on lab activities and 20% to stationary tasks such as data analysis, documentation, and team collaboration. The role involves working directly with a supervisor while interfacing with multiple members of the technical team in a group-oriented setting. Standard hours are Monday through Friday, 8 hours per day. Work is performed in a regulated lab environment that emphasizes safety, cleanliness, and organization, with regular use of laboratory instruments such as HPLC systems, spectroscopy equipment, and particle testing tools. The assignment is initially planned for 12 months and may be extended based on performance and departmental needs.Job Type &amp; LocationThis is a Contract position based out of Waukegan, IL.Pay and BenefitsThe pay range for this position is $22.00 - $25.00/hr.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 Waukegan,IL.Application DeadlineThis position is anticipated to close on Jul 28, 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: Senior Laboratory Technician – 3rd ShiftJob DescriptionThis role offers the opportunity to work as a Senior laboratory technician on the 3rd shift, performing analytical testing and data review using GC/MS and LC/MS/MS instrumentation. You will follow established Standard Operating Procedures, ensure accurate sample processing, and support high-quality, reliable laboratory results while maintaining a safe and compliant work environment.Responsibilities<ul><li>Read, understand, and strictly follow written Standard Operating Procedures for all assigned assays and processes.</li><li>Correctly identify analyzed samples and verify the accuracy and order of the sequence for each batch.</li><li>Process acquired instrument data from GC/MS and LC/MS/MS systems and generate appropriate analytical reports.</li><li>Conduct the first review of GC/MS and/or LC/MS/MS analytical data in accordance with each assay-specific SOP.</li><li>Transcribe or upload test results into the Laboratory Information System (LIS) for final review and certification.</li><li>Maintain proper and complete Chain of Custody documentation for all batches to ensure traceability and compliance.</li><li>Communicate effectively with supervisors regarding daily activities, findings, and issues.</li><li>Promptly escalate emerging challenges, anomalies, or equipment issues to supervisory staff for timely resolution.</li><li>Maintain and promote a safe and healthful environment for self and co-workers by following all laboratory safety procedures.</li><li>Work collaboratively with other laboratory staff to support efficient workflow and consistent quality of results.</li></ul>Essential Skills<ul><li>Bachelor’s degree in chemistry, analytical chemistry, or a closely related scientific field.</li><li>At least one year of experience working in an analytical laboratory environment.</li><li>Ability to work safely with biological specimens, chemicals, laboratory equipment, and analytical instruments.</li><li>Proficiency in following detailed written Standard Operating Procedures.</li><li>Experience with analytical techniques such as GC/MS and/or LC/MS/MS, including data acquisition and review.</li><li>Strong attention to detail for accurate sample identification, sequence verification, and documentation.</li><li>Ability to accurately transcribe or upload analytical results into a Laboratory Information System (LIS).</li><li>Effective communication skills to interact with supervisors and team members and escalate issues promptly.</li><li>Commitment to maintaining proper Chain of Custody documentation and regulatory compliance.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previously demonstrated laboratory experience beyond the minimum requirement is preferred.</li><li>Familiarity with handling and processing biological specimens in a regulated laboratory setting.</li><li>Comfort working with complex analytical instruments and related software systems.</li><li>Strong organizational skills to manage multiple batches and maintain comprehensive documentation.</li><li>Ability to work independently during overnight hours while supporting a team-based laboratory environment.</li></ul>Work EnvironmentThis position is a 3rd shift role with scheduled hours from 10:00 p.m. to 6:30 a.m. You will work in an analytical laboratory environment that uses GC/MS and LC/MS/MS instrumentation, laboratory information systems (LIS), and standard laboratory equipment. The work involves handling biological specimens and chemicals, requiring adherence to laboratory safety procedures, use of appropriate personal protective equipment, and compliance with Chain of Custody and documentation standards. The environment emphasizes safety, accuracy, and collaboration among laboratory professionals to ensure reliable test results and a healthful workplace.Job Type &amp; LocationThis is a Contract position based out of Santa Rosa, CA.Pay and BenefitsThe pay range for this position is $22.50 - $22.50/hr.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 Santa Rosa,CA.Application DeadlineThis position is anticipated to close on Jul 28, 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.

Lab Tech Sr. - 3rd Shift

<h2 style="text-align:center;">Job Title: Lab Assembly Technician</h2>Job DescriptionThe Lab Assembly Technician supports the manufacturing and assembly of solid oxide fuel cell components and systems within an advanced production facility. This role focuses on small-part mechanical and electro-mechanical assembly, ensuring high-quality, reliable products that contribute to next-generation clean energy solutions. The technician applies strong mechanical aptitude, attention to detail, and precision assembly skills to meet strict quality and performance standards.Responsibilities<ul><li>Assemble small mechanical and electro-mechanical components by following detailed work instructions, drawings, and standard operating procedures.</li><li>Perform intricate hand assembly of fuel cell subassemblies and finished products with a high degree of accuracy and care.</li><li>Utilize hand tools, power tools, fixtures, and measurement equipment to complete assembly tasks safely and efficiently.</li><li>Conduct visual inspections and quality checks to verify proper fit, function, and workmanship of components and assemblies.</li><li>Follow manufacturing and quality procedures to ensure all products meet defined specifications and standards.</li><li>Document production activities, inspections, and process data accurately using established documentation systems.</li><li>Maintain a clean, organized, and safe work area in accordance with company safety standards and best practices.</li><li>Assist with packaging, material handling, inventory transactions, and other production support activities as needed.</li><li>Collaborate with Engineering, Manufacturing, and Quality teams to identify, communicate, and help resolve assembly issues.</li><li>Support continuous improvement initiatives focused on enhancing efficiency, product quality, and workplace safety.</li></ul>Essential Skills<ul><li>At least 1 year of experience in manufacturing, assembly, production, or technician roles.</li><li>Experience working with small parts and detailed assembly processes in a production environment.</li><li>Ability to read and follow assembly instructions, work orders, and basic mechanical drawings.</li><li>Strong manual dexterity and hand-eye coordination for precise, intricate assembly work.</li><li>Proficiency in using basic hand tools and measuring devices for assembly and inspection tasks.</li><li>Strong attention to detail and a demonstrated commitment to producing high-quality work.</li><li>Basic computer skills for data entry, production documentation, and recording process data.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in electronics, medical device, aerospace, fuel cell, battery, or precision manufacturing environments.</li><li>Familiarity with lean manufacturing principles and practices.</li><li>Experience working in a regulated or highly quality-focused production environment.</li></ul>Work EnvironmentThis role is based in an advanced manufacturing facility focused on innovative fuel cell technology and scaled production. The work involves hands-on assembly using hand tools, power tools, fixtures, and measurement equipment in a production setting. The environment emphasizes safety, cleanliness, and organization, with strong collaboration among Engineering, Manufacturing, and Quality teams. Shift options include first and second shift openings, with schedules such as Monday to Friday from 4:00 a.m. to 12:30 p.m. and Thursday to Sunday from 6:00 a.m. to 4:30 p.m., supporting continuous operations and production flexibility.Job Type &amp; LocationThis is a Permanent position based out of Mount Pleasant, PA.Pay and BenefitsThe pay range for this position is $41600.00 - $47840.00/yr.100% employee-paid health insurance coverage
Dental insurance
Vision insuranceWorkplace TypeThis is a fully onsite position in Mount Pleasant,PA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Technician

<h3>Lab Technician</h3>Shift: Monday-Friday, 3:00 PM - 11:30 PM<h4>About the Role</h4>Join a growing biotech manufacturing team as a Lab Technician, where you'll play a key role in the production of antibody-based products. This hands-on position is ideal for individuals with laboratory or manufacturing experience who enjoy working in a fast-paced, quality-focused environment. You'll support production operations by dispensing solutions, preparing product kits, operating equipment, maintaining documentation, and ensuring compliance with established procedures.<h4>Key Responsibilities</h4><ul><li>Dispense antibody solutions and other liquid products using precise pipetting and liquid-handling techniques.</li><li>Follow Standard Operating Procedures (SOPs) to formulate products and verify formulation data, including concentrations, calculations, and lot numbers.</li><li>Operate production equipment such as filling lines, labeling machines, and lyophilizers.</li><li>Label, cap, package, and assemble product kits according to production requirements.</li><li>Maintain accurate production records and complete data entry in support of manufacturing activities.</li><li>Store materials properly according to temperature and handling requirements.</li><li>Clean, sanitize, and maintain production equipment and work areas.</li><li>Support day-to-day manufacturing operations and continuous improvement initiatives.</li></ul><h4>Qualifications</h4><ul><li>Minimum 6 months of experience in a laboratory, biotech, pharmaceutical, or manufacturing environment.</li><li>Hands-on experience with liquid dispensing and pipetting is required.</li><li>Familiarity with GMP, GDP, aseptic techniques, and regulated production environments preferred.</li><li>Ability to accurately follow SOPs, work instructions, and documentation requirements.</li><li>Basic math skills and attention to detail for measurements, calculations, and recordkeeping.</li><li>Experience with automated filling equipment is a plus.</li><li>Strong organizational skills and ability to work independently and as part of a team.</li></ul><h4>Why Join?</h4><ul><li>Gain valuable experience in a biotech manufacturing environment.</li><li>Work with regulated production processes and industry-standard equipment.</li><li>Develop skills in GMP manufacturing, documentation, and quality systems.</li><li>Excellent opportunity for candidates looking to build a career in biotechnology, pharmaceuticals, or laboratory operations.</li><li>Potential pathway to future growth within the life sciences industry.</li></ul>Job Type &amp; LocationThis is a Contract position based out of San Diego, CA.Pay and BenefitsThe pay range for this position is $20.00 - $24.00/hr.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 San Diego,CA.Application DeadlineThis position is anticipated to close on Aug 3, 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: Lab TechnicianJob DescriptionThe Lab Technician will be responsible for maintaining plating baths and overseeing wastewater treatment operations onsite in the plant. This role involves walking the plant floor each morning with an iPad to record any variations or issues, and making necessary adjustments by adding chemicals. The technician will handle chemical baths, which require lifting bags weighing up to 55 lbs, and take water samples three times a day for lab testing, including pH, titrations, and color testing. Results must be recorded and entered into the system accurately. The technician will also change bag filters, clean the clarifier weekly, and perform maintenance on treatment equipment with full training provided.Responsibilities<ul><li>Maintain plating baths and wastewater treatment operations.</li><li>Conduct morning plant floor inspections using an iPad to record issues.</li><li>Adjust chemical baths by adding necessary chemicals.</li><li>Lift and handle bags of chemicals up to 55 lbs.</li><li>Take and test water samples three times daily, including pH, titrations, and color testing.</li><li>Record and enter testing results into the system accurately.</li><li>Change bag filters and clean clarifiers weekly.</li><li>Perform weekly maintenance on treatment equipment.</li></ul>Essential Skills<ul><li>Proficient in titrations, pH testing, and color testing.</li><li>Knowledge of acid and base chemicals.</li><li>Experience in a manufacturing environment.</li><li>Bachelor's degree in Chemistry, Biochemistry, or equivalent experience.</li><li>Mechanically inclined and comfortable in a manufacturing setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in Chemistry preferred.</li><li>Familiarity with plating processes and wastewater treatment systems.</li><li>Previous lab experience outside of academic settings is a plus.</li></ul>Work EnvironmentThe Lab Technician will work in both a lab and wastewater treatment area within a plant that coats automotive parts with protective and semi-decorative coatings. The environment is not spotless, but equipped with modern analytical instruments for testing. The lab team is small and collaborative, consisting of one other technician and the Lab Manager. The company operates privately with a friendly, yet precise working atmosphere where accuracy and timely reporting are priorities. The role requires working Monday to Friday from 8 am to 4:30 pm, with no travel required.Job Type &amp; LocationThis is a Contract to Hire position based out of Warren, MI.Pay and BenefitsThe pay range for this position is $20.00 - $21.00/hr.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 Warren,MI.Application DeadlineThis position is anticipated to close on Aug 7, 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: Lab TechnicianJob DescriptionAs a Lab Technician, you will ensure the quality of batch preparation and quality control activities, including process inspection, sampling, and evaluation to meet specification and quality standards. You will be responsible for testing incoming and outgoing products for suitability and compliance with appropriate standards, such as pH, TA, fat, salt, and moisture.Responsibilities<ul><li>Properly test incoming and outgoing products for suitability and compliance with appropriate standards.</li><li>Perform sample setup, sorting, preparation, and clean-up.</li><li>Calibrate and maintain laboratory instrumentation as directed.</li><li>Notify supervisor of any out-of-range values or variations from accepted norms immediately.</li><li>Maintain lab records accurately, clearly, and timely. Complete data entry into the computer system(s).</li><li>Prepare reports of results and maintain process control by monitoring and generating statistical information.</li><li>Participate in task meetings and suggest changes in work tasks and use of equipment to increase efficiencies.</li><li>Perform daily cleaning of task area, keeping work area free of clutter, and detail cleaning during CIP.</li><li>Maintain safe working conditions and compliance with all state and federal regulations regarding health and safety.</li><li>Follow all good manufacturing practices (GMP) and work in accordance with regulatory, food safety, quality, and sanitation requirements.</li></ul>Essential Skills<ul><li>Minimum of 6 months food manufacturing quality lab experience.</li><li>Strong critical thinking skills.</li><li>Ability to work in a fast-paced environment.</li><li>Proficient in time management.</li><li>Flexibility to adapt to production needs.</li><li>Familiarity with Microsoft Office and quality assurance.</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Belvidere, IL.Pay and BenefitsThe pay range for this position is $66476.80 - $66476.80/yr.$1 increase on work anniversary.Workplace TypeThis is a fully onsite position in Belvidere,IL.Application DeadlineThis position is anticipated to close on Jul 27, 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: Lab Technician Job DescriptionThe Lab Technician is accountable for ensuring the integrity of our product during the manufacturing process and through release. This position requires the use of standardized techniques and operating procedures to conduct and analyze tests on sensitive samples. As a critical member of the Quality Team, this role promotes a culture of Quality and Food Safety.Responsibilities<ul><li>Exemplify core values of Integrity, Respect, Excellence, Resourcefulness, and Teamwork in daily activities.</li><li>Adhere to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and HACCP requirements.</li><li>Pass all required laboratory training.</li><li>Follow established Standard Operating Procedures (SOPs) accurately and efficiently.</li><li>Record, interpret, and enter test results into specified forms and LIMS software accurately and responsibly.</li><li>Perform analytical and sensory tests on in-process and finished products precisely and timely.</li><li>Identify inconsistencies in data and report to necessary personnel, including escalation when needed.</li><li>Receive, handle, and store samples according to SOPs.</li><li>Maintain and troubleshoot laboratory equipment, taking corrective action when necessary and keeping records.</li><li>Handle, organize, and store chemicals, fluids, and compressed gases as outlined in Safety Data Sheets.</li><li>Work independently and in teams across departments.</li><li>Complete verifications in testing, standards, equipment, and instruments to ensure accuracy.</li><li>Participate in proficiency and collaborative testing.</li><li>Communicate with other departments as necessary through various methods.</li><li>Show willingness to take on additional responsibilities.</li><li>Perform routine tasks with minimal supervision.</li><li>Maintain a neat, clean, and professional work area.</li><li>Train colleagues as needed.</li><li>Perform all duties in compliance with environmental, health, and safety policies.</li><li>Assume QC Specialist and Manager responsibilities when required.</li><li>Maintain samples of tested products to confirm test results when needed.</li><li>Ensure adequate supplies for testing and notify the manager when reordering is necessary.</li><li>Continuously compare test results with standards to ensure product specifications are met.</li></ul>Essential Skills<ul><li>Laboratory and lab experience</li><li>Strong computer skills</li><li>Ability to work in a fast-paced environment</li></ul>Additional Skills &amp; Qualifications<ul><li>Preferred analytical laboratory experience</li></ul>Work EnvironmentThe position involves working off-shift hours, with possible schedules including a Swing Shift (Monday 7AM-3PM, Tuesday 11PM-7AM, Wednesday 11PM-7AM, Thursday 3PM-11PM, Friday 3PM-11PM) or a 3rd Shift (Monday 11PM-7AM, OFF Tuesday/Wednesday, Thursday-Saturday 11PM-7AM, Sunday 11PM-11AM).Job Type &amp; LocationThis is a Contract position based out of Chattanooga, TN.Pay and BenefitsThe pay range for this position is $23.00 - $23.00/hr.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 Chattanooga,TN.Application DeadlineThis position is anticipated to close on Jul 30, 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.

Description
					Laboratory Technician
Position Summary

We are seeking a motivated Laboratory Technician to support quality and laboratory operations in a manufacturing environment producing products such as toilet bowl cleaners, bleach, and dry pool tablets. This role is responsible for collecting and testing production and water samples, documenting results, and ensuring compliance with quality standards and GMP requirements. The ideal candidate is self-motivated, able to work independently, and committed to continuous learning and development.

Schedule
Initial operation will support 1st and 2nd shifts
Planned transition to a 3-shift operation within the first year
Training will be conducted on 1st Shift (7:00 AM – 3:30 PM) for approximately 2 weeks to 1 month
Current openings:
1st Shift: 7:00 AM – 3:30 PM
2nd Shift: 3:00 PM – 11:30 PM
Responsibilities
Collect production samples from manufacturing lines every 3 hours
Perform laboratory testing on raw materials, in-process, and finished products
Conduct analyses including:
Moisture testing
pH testing
Viscosity testing
Basic microbiological and rapid testing methods
Collect and analyze water samples as required
Utilize FTIR (Fourier Transform Infrared Spectroscopy) equipment for testing and analysis
Accurately document test results and maintain laboratory records
Follow all Good Manufacturing Practices (GMPs) and laboratory procedures
Communicate quality concerns and deviations to appropriate personnel
Maintain a clean, organized, and safe laboratory environment
Support continuous improvement initiatives and process development activities
Qualifications
Required
Bachelor's degree in Chemistry, Biology, Microbiology, or a related scientific field preferred
Minimum 1 year of chemistry laboratory experience preferred
Strong understanding of Good Manufacturing Practices (GMPs) (highly important)
Ability to work independently and manage workload with minimal supervision
Strong attention to detail and organizational skills
Ability to take initiative and proactively solve problems
Desire to continually learn, develop, and expand technical skills
Comfortable collecting samples from manufacturing lines and production areas
Preferred
Experience with FTIR instrumentation
Experience in a manufacturing, consumer products, chemical, or quality laboratory environment
Exposure to microbiological testing methods
Recent graduates with relevant laboratory coursework, internships, or research experience are encouraged to apply
Physical Requirements
Ability to work in a manufacturing and laboratory environment
Ability to stand, walk, and collect samples throughout the facility
Ability to lift sample containers and laboratory materials as needed
PPE requirements, including steel-toe footwear, will be determined based on facility safety requirements
Key Traits for Success
Self-directed and dependable
Strong sense of ownership and accountability
Takes initiative without waiting for direction
Adaptable in a growing operation
Committed to quality, safety, and continuous improvement
Eager to learn and grow within the organization
										Skills
					Quality control, Chemistry, Laboratory, Gmp, Quality assurance, Microbiology, Wet chemistry, Analytical chemistry
										Top Skills Details
					Quality control,Chemistry,Laboratory,Gmp,Quality assurance,Microbiology,Wet chemistry,Analytical chemistry
										
					
										Experience Level
					Entry Level
					Job Type &amp; LocationThis is a Contract position based out of Wixom, MI.Pay and BenefitsThe pay range for this position is $20.00 - $25.00/hr.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 Wixom,MI.Application DeadlineThis position is anticipated to close on Jul 31, 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>Actively Screening for Lab Technician - Chemist to join product repair company in Marietta, GA! </h2>﻿Job DescriptionThe Lab Technician will engage in daily lab tasks to support the development of new paint formulas. This includes preparing panels, monitoring dry times, conducting adhesion tests, and documenting results. The role involves working 50% in the lab, 30% in documentation, and 20% in communication with external labs and team members.Responsibilities<ul><li>Conduct laboratory testing including viscosity, lap shear adhesion, and tensile strength, with a focus on adhesives, sealants, and coatings.</li><li>Prepare, conduct, and report on product testing and development.</li><li>Maintain detailed and organized documentation of work performed.</li><li>Practice safe work habits and comply with all Environmental, Health, and Safety policies and regulations.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>Experience in chemistry, formulation, and laboratory settings.</li><li>3+ years of experience with silicone, epoxy, consumer adhesive, polyester, or polyurethane.</li><li>BS in Chemistry, Polymer Science, or Chemical Engineering.</li><li>Experience with pencil hardness testing, posi testing, cross-hatch testing, and new product development.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in a lab setting with independent execution of test procedures.</li><li>Relevant college degree or equivalent experience.</li><li>Fluency in English.</li><li>Eligible to work in the USA.</li><li>Ability to lift, pull, and push up to 35 lb.</li><li>Basic computer skills including proficiency with MS Office applications.</li><li>Ability to work on both self-directed and team-oriented projects.</li><li>Excellent quantitative math skills and strong written/verbal communication skills.</li><li>Strong attention to detail.</li></ul>Work EnvironmentThe Lab Technician will work from 8 AM to 4 PM, Monday through Friday, totaling 40 hours per week. The position is based in a lab environment with mixing equipment and an outdoor area for spraying panels. The lab is divided into two large rooms, and a computer will be provided for documentation. Candidates will work around paint and solvents, with a respirator available upon request. The team comprises 7 members within a company of approximately 15-175 employees, with 20-30 based in Atlanta. Less than 10% travel is required.Job Type &amp; LocationThis is a Contract position based out of Marietta, GA.Pay and BenefitsThe pay range for this position is $30.00 - $40.00/hr.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 Marietta,GA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Actively Hiring for Lab Assistant to join top medical laboratory in Norcross, GA!Job DescriptionAs a Lab Assistant, you will be responsible for performing various duties assigned by the department, maintaining accurate records and documentation, recognizing unusual results and resolving discrepancies, and communicating unusual occurrences to management.Responsibilities<ul><li>Perform SATR.</li><li>Operate P512.</li><li>Receive and sort boxes.</li><li>Sort samples.</li><li>Operate IDETIC as assigned.</li><li>Conduct sample investigations.</li><li>Dispose of biohazard materials.</li></ul>Essential Skills<ul><li>Experience in laboratory settings.</li><li>Proficient in sample handling and accessioning.</li><li>Ability to conduct data entry efficiently.</li><li>Knowledge of inventory management, SOP, and quality control.</li></ul>Work EnvironmentWarehouse and laboratory environment Lab Assistant | Day shift (Sunday-Wednesday)Regular Schedule: Sunday–Wednesday, 7:00 AM – 5:30 PMTraining Schedule: Sunday–Tuesday: 10:00 AM – 10:30 PM (training schedule may change depending on needs)Need to be able to start within the next week and not currently working any other job. Job Type &amp; LocationThis is a Contract position based out of Norcross, GA.Pay and BenefitsThe pay range for this position is $18.00 - $18.00/hr.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 Norcross,GA.Application DeadlineThis position is anticipated to close on Aug 3, 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: Lab TechnicianJob DescriptionA consumer product tobacco alternative organization is seeking a Lab Technician for their Quality Control (QC) Team. The role is based in Durham, NC, and involves supporting the Chemistry and Regulatory Testing and regulatory submissions. The Lab Technician will be a hands-on, laboratory-based role responsible for testing products for regulatory submissions. The ideal candidate is highly motivated, adaptable, and effective in a fast-paced environment, capable of collaborating well with other team members.Responsibilities<ul><li>Perform preparation of e-liquid and aerosol samples for analysis.</li><li>Conduct non-chromatographic methods on e-liquids and aerosol samples, such as pH, water activity, density, and particle sizing.</li><li>Collect aerosol samples routinely from ENDS devices.</li><li>Prepare reagents for laboratory usage.</li><li>Clean laboratory glassware.</li><li>Receive and log samples and supplies into the Laboratory Information Management System (LIMS).</li><li>Write and review scientific documents in a timely manner, including SOPs, VOPs, and Work Instructions.</li><li>Manage regulatory documents systematically in a highly organized fashion.</li><li>Perform other related duties as assigned.</li></ul>Essential Skills<ul><li>At least one year of experience in an analytical laboratory is preferred.</li><li>Strong pipetting and weighing skills.</li><li>Ability to prepare clear and concise written documents.</li><li>Strong problem-solving skills.</li><li>High motivation and flexibility.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with vaping machines and collection techniques is preferred.</li><li>ENDS or nicotine-related products experience is preferred.</li><li>Experience in a regulated laboratory environment such as ISO is preferred.</li><li>Bachelor's or Associate's degree in Chemistry or previous experience in a chemistry lab.</li></ul>Work EnvironmentThe position is based on-site in Durham, NC, operating during normal business hours. The work is conducted in a vapor lab environment, focusing on preparation for quality control rather than direct testing. This smaller lab offers growth opportunities, as evidenced by team members advancing to roles in QA or running instruments such as GCMS.Job Type &amp; LocationThis is a Contract to Hire position based out of Durham, NC.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.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 Jul 31, 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: Lab TechnicianJob DescriptionA consumer product tobacco alternative organization is seeking a Lab Technician for their Quality Control (QC) Team. The role is based in Durham, NC, and involves supporting the Chemistry and Regulatory Testing and regulatory submissions. The Lab Technician will be a hands-on, laboratory-based role responsible for testing products for regulatory submissions. The ideal candidate is highly motivated, adaptable, and effective in a fast-paced environment, capable of collaborating well with other team members.Responsibilities<ul><li>Perform preparation of e-liquid and aerosol samples for analysis.</li><li>Conduct non-chromatographic methods on e-liquids and aerosol samples, such as pH, water activity, density, and particle sizing.</li><li>Collect aerosol samples routinely from ENDS devices.</li><li>Prepare reagents for laboratory usage.</li><li>Clean laboratory glassware.</li><li>Receive and log samples and supplies into the Laboratory Information Management System (LIMS).</li><li>Write and review scientific documents in a timely manner, including SOPs, VOPs, and Work Instructions.</li><li>Manage regulatory documents systematically in a highly organized fashion.</li><li>Perform other related duties as assigned.</li></ul>Essential Skills<ul><li>At least one year of experience in an analytical laboratory is preferred.</li><li>Strong pipetting and weighing skills.</li><li>Ability to prepare clear and concise written documents.</li><li>Strong problem-solving skills.</li><li>High motivation and flexibility.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with vaping machines and collection techniques is preferred.</li><li>ENDS or nicotine-related products experience is preferred.</li><li>Experience in a regulated laboratory environment such as ISO is preferred.</li><li>Bachelor's or Associate's degree in Chemistry or previous experience in a chemistry lab.</li></ul>Work EnvironmentThe position is based on-site in Durham, NC, operating during normal business hours. The work is conducted in a vapor lab environment, focusing on preparation for quality control rather than direct testing. This smaller lab offers growth opportunities, as evidenced by team members advancing to roles in QA or running instruments such as GCMS.Job Type &amp; LocationThis is a Contract to Hire position based out of Durham, NC.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.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 Jul 28, 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: Lab TechnicianJob DescriptionA consumer product tobacco alternative organization is seeking a Lab Technician for their Quality Control (QC) Team. The role is based in Durham, NC, and involves supporting the Chemistry and Regulatory Testing and regulatory submissions. The Lab Technician will be a hands-on, laboratory-based role responsible for testing products for regulatory submissions. The ideal candidate is highly motivated, adaptable, and effective in a fast-paced environment, capable of collaborating well with other team members.Responsibilities<ul><li>Perform preparation of e-liquid and aerosol samples for analysis.</li><li>Conduct non-chromatographic methods on e-liquids and aerosol samples, such as pH, water activity, density, and particle sizing.</li><li>Collect aerosol samples routinely from ENDS devices.</li><li>Prepare reagents for laboratory usage.</li><li>Clean laboratory glassware.</li><li>Receive and log samples and supplies into the Laboratory Information Management System (LIMS).</li><li>Write and review scientific documents in a timely manner, including SOPs, VOPs, and Work Instructions.</li><li>Manage regulatory documents systematically in a highly organized fashion.</li><li>Perform other related duties as assigned.</li></ul>Essential Skills<ul><li>At least one year of experience in an analytical laboratory is preferred.</li><li>Strong pipetting and weighing skills.</li><li>Ability to prepare clear and concise written documents.</li><li>Strong problem-solving skills.</li><li>High motivation and flexibility.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with vaping machines and collection techniques is preferred.</li><li>ENDS or nicotine-related products experience is preferred.</li><li>Experience in a regulated laboratory environment such as ISO is preferred.</li><li>Bachelor's or Associate's degree in Chemistry or previous experience in a chemistry lab.</li></ul>Work EnvironmentThe position is based on-site in Durham, NC, operating during normal business hours. The work is conducted in a vapor lab environment, focusing on preparation for quality control rather than direct testing. This smaller lab offers growth opportunities, as evidenced by team members advancing to roles in QA or running instruments such as GCMS.Job Type &amp; LocationThis is a Contract to Hire position based out of Durham, NC.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.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 Aug 7, 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: Lab Technician Job DescriptionThis Lab Technician role focuses on performing routine and specialized testing on crude oil, base oils, lube oils, and petrochemical products in a high-volume laboratory. The technician operates and interprets results from analytical instruments, maintains accurate records in the laboratory information management system (LIMS), and follows established safety and standard operating procedures. This position supports quality control activities within the petroleum industry and plays a key role in ensuring reliable and timely test results.Responsibilities<ul><li>Run routine tests on crude oil, base oils, lube oils, and petrochemical samples in accordance with established laboratory procedures.</li><li>Set up, operate, and interpret results from gas chromatographs (GC) and inductively coupled plasma (ICP) instruments.</li><li>Perform wet chemistry analyses, including titrations and distillations, following standard methods.</li><li>Operate octane engines and related equipment as required for petroleum product testing.</li><li>Accurately enter and maintain test data in the laboratory LIMS system, ensuring data integrity and traceability.</li><li>Follow laboratory standard operating procedures (SOPs) and safety protocols at all times.</li><li>Maintain laboratory inventory by monitoring supplies, reagents, and consumables, and notifying appropriate personnel when restocking is needed.</li><li>Ensure instruments and equipment are kept in good working order by performing basic maintenance and reporting issues promptly.</li><li>Work collaboratively with other lab staff to meet testing schedules and quality control requirements.</li><li>Support continuous improvement of laboratory processes by following best practices and providing feedback on workflow and procedures.</li></ul>Essential Skills<ul><li>2–5 years of experience working with ICP instrumentation.</li><li>2–5 years of experience working with octane engines in a laboratory or petroleum testing environment.</li><li>Hands-on experience running, setting up, and interpreting data from GC and ICP instruments.</li><li>Prior experience using a laboratory information management system (LIMS).</li><li>Experience in the petroleum industry, including exposure to crude oil, base oils, lube oils, and petrochemical testing.</li><li>Proficiency in wet chemistry techniques such as titration and distillation.</li><li>A.S. or B.S. degree in Chemistry, Biology, or a related field.</li><li>Completion of at least one in-person laboratory course during their academic program, ideally in chemistry.</li><li>Ability to stand and be on their feet for extended periods, including 12-hour shifts.</li><li>Willingness and ability to work rotating shift schedules, including day and night shifts.</li><li>Comfort working in an oil and gas laboratory environment.</li><li>Strong attention to detail and accuracy in data entry and recordkeeping.</li><li>Ability to follow detailed SOPs and safety protocols consistently.</li></ul>Additional Skills &amp; Qualifications<ul><li>Degree specialization in Chemistry or a closely related life science discipline.</li><li>Prior quality control laboratory experience.</li><li>Familiarity with testing methodologies specific to crude oil, base oils, lube oils, and petrochemical products.</li><li>Experience working in a high-throughput industrial or production laboratory.</li><li>Strong problem-solving skills for troubleshooting instrumentation and test anomalies.</li><li>Effective communication skills to collaborate with colleagues and report results clearly.</li><li>Organizational skills to manage multiple tests, samples, and priorities during long shifts.</li></ul>Work EnvironmentThe Lab Technician works in an oil and gas laboratory environment that focuses on testing crude oil, base oils, lube oils, and petrochemical products. The role follows a rotating 2-3-3-2 shift schedule, with two weeks of day shifts from 6:00 a.m. to 6:00 p.m., followed by two weeks of night shifts from 6:00 p.m. to 6:00 a.m. The position requires being on your feet for up to 12 hours per shift and working around analytical instruments such as GC, ICP, and octane engines, as well as wet chemistry benches for titrations and distillations. The laboratory operates under defined safety protocols and standard operating procedures, and team members are expected to adhere to all safety guidelines and use appropriate personal protective equipment while performing their duties.Job Type &amp; LocationThis is a Contract to Hire position based out of Gonzales, LA.Pay and BenefitsThe pay range for this position is $24.00 - $26.00/hr.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 Gonzales,LA.Application DeadlineThis position is anticipated to close on Jul 27, 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.

DescriptionPerforms chemical and instrumental analysis on fuels, oils, and other lubricants using standard testing methods as prescribed by ASTM(testing standards). Performs analyses on any new sample introduced. Prepare solutions or solvents for various tests; transfers samples from one area to another in the lab; maintains workbooks and equipment on a daily, weekly and monthly basis as per sop and tip test procedures. There is a fuel/oil smell with these samples. *Industrial Lab Setting- Research on automotive productsShift - 6am- 3pm, 8-pm, 3- 11pm - Monday - Friday. Occasional weekend work. SkillsLab environment, sample preparation, ms office suite, math calculations, washing galsswareTop Skills DetailsLab environment,sample preparation,ms office suite,math calculations,washing galsswareAdditional Skills &amp; QualificationsHigh School diplomaCandidate muse have one year of college chemistry and math or one year of related laboratory experience. Candidate must be able to lift and transporting 50lbs. familiar with basic lab safetyTraining is provided- all hands on- shadowingExperience LevelEntry LevelJob Type &amp; LocationThis is a Contract position based out of San Antonio, TX.Pay and BenefitsThe pay range for this position is $15.50 - $15.50/hr.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 San Antonio,TX.Application DeadlineThis position is anticipated to close on Jul 27, 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: Process Technician Job DescriptionThe Process Technician plays a key role in manufacturing sensing elements used in advanced detection systems. This role operates production equipment, prepares and monitors chemical-based batches, and performs in-process testing to ensure products meet strict specifications. The Process Technician follows detailed Standard Operating Procedures and instructions to fabricate, inspect, and package products while maintaining accurate production and inventory records. This position directly supports the development of cutting-edge technologies that contribute to safety and protection in critical applications.Responsibilities<ul><li>Operate manufacturing equipment to produce sensing elements and chemical-based products according to Standard Operating Procedures and manufacturing documentation.</li><li>Weigh, measure, and verify raw materials to ensure batches contain the correct ingredients in the proper quantities.</li><li>Maintain accurate and up-to-date inventory records of raw materials used in batch manufacturing.</li><li>Complete and maintain detailed batch records and data sheets for batches in process and finished products.</li><li>Perform in-process tests, including hardness, weight, variation, pH, and moisture content, to ensure batches meet specifications.</li><li>Recognize equipment and product issues, notify appropriate personnel, and assist in troubleshooting to maintain optimal production levels.</li><li>Manually assemble mechanical parts into sub-units or complete units in accordance with assembly instructions, process documents, and travelers.</li><li>Perform mechanical assembly work involving pneumatic and optical micro assemblies.</li><li>Conduct leak checks and create vacuum seals on equipment as required by the process.</li><li>Wire electronic components into sub-units or complete units following manufacturing documentation.</li><li>Assemble parts into sub-assemblies and complete units, including process assembly, inspection, modifications, upgrades, and rework.</li><li>Manually assemble and package products, ensuring correct labeling, documentation, and quality standards.</li><li>Fabricate, inspect, and package chemical-based products safely and accurately.</li><li>Organize materials and maintain orderly, efficient work areas.</li><li>Accurately complete production records, logs, and data sheets using relevant computer applications.</li><li>Identify and suggest opportunities for process and workflow improvements as part of continuous improvement initiatives.</li><li>Maintain a clean, safe, and organized working environment in compliance with safety and quality standards.</li><li>Handle laboratory equipment, tools, and chemicals safely and responsibly in accordance with established procedures.</li><li>Collaborate with team members while being able to work independently at a designated workbench.</li><li>Communicate effectively with colleagues and supervisors regarding production status, issues, and improvement ideas.</li></ul>Essential Skills<ul><li>Ability to follow written Standard Operating Procedures and verbal instructions to fabricate, inspect, and package products.</li><li>Experience operating manufacturing equipment and working in an assembly or production environment.</li><li>Good organizational skills with the ability to manage materials, work areas, and documentation efficiently.</li><li>Proficiency with relevant computer applications, including Microsoft Office, for maintaining production and batch records.</li><li>Ability to safely handle laboratory equipment, tools, and chemicals.</li><li>Mechanical assembly skills, including assembling mechanical parts into sub-units or complete units using manufacturing documentation.</li><li>Understanding of mechanical assembly concepts, including pneumatic and optical micro assemblies.</li><li>Ability to perform leak checks and create vacuum seals on equipment.</li><li>Basic electrical wiring skills to wire electronic components into sub-units or complete units following documentation.</li><li>Experience performing in-process testing such as hardness, weight, variation, pH, and moisture content.</li><li>Strong attention to detail and accuracy in measurements, documentation, and assembly work.</li><li>Good manual dexterity for handling small components and precise assembly tasks.</li><li>Ability to recognize equipment and product problems and support troubleshooting efforts.</li><li>Self-motivation, dependability, and strong communication skills for working effectively in a team environment.</li><li>Ability to lift up to 50 pounds from ground to table height.</li><li>Associate’s degree or a High School diploma/GED with 3 or more years of experience in an assembly or production environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Prior experience in assembly or production environments involving lean manufacturing practices.</li><li>Background or experience with process improvement and continuous improvement initiatives.</li><li>Exposure to process engineering or manufacturing process optimization.</li><li>Prior experience working with laboratory equipment.</li><li>Background in chemistry or biology.</li><li>Experience working in clean, climate-controlled production or laboratory environments.</li><li>Interest and ability to quickly learn new work operations and technologies.</li><li>Experience in environments focused on safety-critical or high-technology products, such as detection systems.</li><li>Familiarity with bomb detection, chemical and biohazard detection, or illegal drug detection technologies is beneficial but not required.</li><li>Experience with inspection, modifications, upgrades, and rework of assembled units.</li></ul>Work EnvironmentThis role is based on-site in a clean, climate-controlled facility and requires working in the office five days per week. The Process Technician primarily works at a designated test workbench, performing detailed assembly, testing, and documentation tasks. The environment emphasizes safety, precision, and cleanliness, with regular handling of laboratory equipment, tools, and chemicals under established procedures. You will work as part of a collaborative team while performing many tasks independently at your workstation. The facility supports advanced manufacturing and testing of cutting-edge detection technologies, providing a structured, organized setting where continuous improvement and high-quality standards are central to daily operations.Job Type &amp; LocationThis is a Contract position based out of West Lafayette, IN.Pay and BenefitsThe pay range for this position is $25.00 - $31.00/hr.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 West Lafayette,IN.Application DeadlineThis position is anticipated to close on Jul 30, 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: Lab TechnicianJob DescriptionThis Lab Technician role supports a growing manufacturing facility by performing quality assurance and quality control testing on liquid products in a plant and laboratory environment. You will collect samples from production silos, perform analytical tests using laboratory instruments, and ensure all products meet strict FDA, plant, and quality specifications. This position offers the opportunity to develop technical skills in chemistry, microbiology, and analytical testing while contributing directly to safe and consistent product quality.Responsibilities<ul><li>Navigate the plant environment safely to obtain liquid samples from silos in accordance with FDA and plant standards, maintaining awareness of machinery and forklifts at all times.</li><li>Collect and handle samples carefully to prevent contamination and ensure they accurately represent production batches.</li><li>Perform laboratory tests on samples, including pH, acidity, freezing point or related critical control points, viscosity, and solid/fat percentage measurements, ensuring results remain within specified ranges.</li><li>Operate, monitor, and maintain laboratory instruments and equipment used for analytical chemistry, titration, and other quality control tests.</li><li>Document all test results accurately with dates, signatures, and relevant details, ensuring complete and traceable quality records.</li><li>Review and verify quality standards and specifications, escalating any out-of-specification results or trends to appropriate personnel.</li><li>Calibrate laboratory equipment daily and perform routine checks to ensure instruments remain accurate and reliable.</li><li>Follow FDA regulations, Good Manufacturing Practices (GMP), and internal plant standards consistently in both the lab and production areas.</li><li>Maintain a clean, organized, and sanitary laboratory environment to prevent contamination and ensure safe operations.</li><li>Monitor and replenish laboratory supplies such as chemicals, pipettes, and other consumables to support continuous testing.</li><li>Handle incoming phone calls from the dairy and various parts of the plant, coordinating sample testing and communicating results as needed.</li><li>Multitask throughout the shift to manage multiple samples, tests, and requests while maintaining accuracy and efficiency.</li><li>Support quality assurance and quality control programs by performing inspections, documenting findings, and contributing to continuous improvement efforts.</li><li>Enter data accurately into laboratory or quality systems, ensuring timely and complete reporting of all test results.</li><li>Collaborate with production and quality teams to ensure products and samples move forward in the process only when they meet specification.</li></ul>Essential Skills<ul><li>Bachelor’s degree in a technical science discipline such as chemistry, biology, microbiology, or a related field.</li><li>At least 1 year of experience working in a manufacturing environment.</li><li>Demonstrated ability to document and review quality standards and specifications accurately.</li><li>Experience with quality assurance and quality control practices in a manufacturing or laboratory setting.</li><li>Hands-on experience with laboratory instrumentation and analytical testing.</li><li>Knowledge of chemistry, analytical chemistry, and related laboratory techniques.</li><li>Familiarity with microbiology or biology concepts relevant to product quality and safety.</li><li>Understanding of Good Manufacturing Practices (GMP) and their application in a plant or lab environment.</li><li>Ability to perform titration and other quantitative analytical methods.</li><li>Strong attention to detail and accuracy in testing, documentation, and data entry.</li><li>Ability to work safely in a manufacturing plant environment, including awareness around machinery and forklifts.</li><li>Capability to multitask and manage multiple priorities in a fast-paced setting.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience working in a quality assurance or quality control role within a manufacturing facility.</li><li> inspection and analytical chemistry within a production or food-related environment.</li><li>Comfort using laboratory information systems or digital tools for data entry and recordkeeping.</li><li>Strong communication skills to coordinate with dairy operations, production staff, and other plant departments.</li><li>Interest in long-term growth within a manufacturing and laboratory setting, including potential internal movement after successful performance.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Elma, NY.Pay and BenefitsThe pay range for this position is $23.25 - $23.25/hr.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 Elma,NY.Application DeadlineThis position is anticipated to close on Aug 3, 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: Lab TechnicianJob DescriptionA consumer product tobacco alternative organization is seeking a Lab Technician for their Quality Control (QC) Team. The role is based in Durham, NC, and involves supporting the Chemistry and Regulatory Testing and regulatory submissions. The Lab Technician will be a hands-on, laboratory-based role responsible for testing products for regulatory submissions. The ideal candidate is highly motivated, adaptable, and effective in a fast-paced environment, capable of collaborating well with other team members.Responsibilities<ul><li>Perform preparation of e-liquid and aerosol samples for analysis.</li><li>Conduct non-chromatographic methods on e-liquids and aerosol samples, such as pH, water activity, density, and particle sizing.</li><li>Collect aerosol samples routinely from ENDS devices.</li><li>Prepare reagents for laboratory usage.</li><li>Clean laboratory glassware.</li><li>Receive and log samples and supplies into the Laboratory Information Management System (LIMS).</li><li>Write and review scientific documents in a timely manner, including SOPs, VOPs, and Work Instructions.</li><li>Manage regulatory documents systematically in a highly organized fashion.</li><li>Perform other related duties as assigned.</li></ul>Essential Skills<ul><li>At least one year of experience in an analytical laboratory is preferred.</li><li>Strong pipetting and weighing skills.</li><li>Ability to prepare clear and concise written documents.</li><li>Strong problem-solving skills.</li><li>High motivation and flexibility.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with vaping machines and collection techniques is preferred.</li><li>ENDS or nicotine-related products experience is preferred.</li><li>Experience in a regulated laboratory environment such as ISO is preferred.</li><li>Bachelor's or Associate's degree in Chemistry or previous experience in a chemistry lab.</li></ul>Work EnvironmentThe position is based on-site in Durham, NC, operating during normal business hours. The work is conducted in a vapor lab environment, focusing on preparation for quality control rather than direct testing. This smaller lab offers growth opportunities, as evidenced by team members advancing to roles in QA or running instruments such as GCMS.Job Type &amp; LocationThis is a Contract to Hire position based out of Durham, NC.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.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 Aug 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>Chemistry Technician </h2>Long-Term Opportunity | Excellent Growth Opportunity | Offers Benefits Job DescriptionThe Chemistry Technician supports the Quality team by performing sample logging, testing, condition monitoring, and general lab upkeep. This role works closely with the R&amp;D team, handling samples and performing production floor checks to ensure that high-performance petroleum products meet workmanship and quality standards. The Lab Technician uses instrumental analysis to support blending and packaging operations, performs day-to-day monitoring and testing, and provides initial start-up authorization to ensure reliability and conformance to specifications.Responsibilities<ul><li>Log and receive samples, perform in-process testing, and maintain accurate records of all laboratory activities.</li><li>Conduct condition monitoring and run laboratory tests to support the Quality department and production operations.</li><li>Perform pipetting, titrations, fuel dilution testing, labeling, barcoding, and other wet chemistry techniques in accordance with lab quality standards.</li><li>Execute laboratory tests throughout the full product life cycle, including but not limited to FTIR, viscosity, density, XRF, and ICP analyses.</li><li>Calibrate, validate, and troubleshoot laboratory instruments to ensure accurate and reliable test results.</li><li>Generate test results using the LIMS system and prepare clear, complete test reports as required.</li><li>Maintain lab quality standards at all times, ensuring continuous documentation of results, records, and all other required reports.</li><li>Support the blending and packaging functions of high-performance petroleum products through timely and accurate testing and approvals.</li><li>Perform routine lab upkeep, including organization, cleanliness, and readiness of instruments and work areas.</li><li>Conduct production floor quality control checks as needed to verify conformance to specifications.</li><li>Work independently during designated hours while maintaining communication with the broader Quality and lab teams.</li><li>Contribute positively to the lab’s outgoing and collaborative culture by communicating effectively and supporting team goals.</li></ul>Essential Skills<ul><li>Bachelor’s degree in Chemistry or related laboratory sciences coursework.</li><li>6–12 months of academic or quality laboratory experience.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Minneapolis, MN.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr.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 Minneapolis,MN.Application DeadlineThis position is anticipated to close on Aug 3, 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: Lab TechnicianJob DescriptionThis Lab Technician role focuses on conducting chemical and physical laboratory tests that support qualitative and quantitative analysis of solids, liquids, and gaseous materials. You will work closely with scientists, chemists, and engineers to support research and development, quality assurance, and production processes. Depending on project needs, you may work in an experimental laboratory as a research technician or in a manufacturing setting as a process control technician, helping ensure products meet stringent quality and safety standards.Responsibilities<ul><li>Monitor product quality to ensure compliance with established standards, specifications, and regulatory expectations.</li><li>Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation methods, and microscopy.</li><li>Perform chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials.</li><li>Compile, analyze, and interpret test data, ensuring results are accurate, reliable, and clearly documented.</li><li>Provide technical support and assistance to chemists, engineers, and other technical staff in both research and process control environments.</li><li>Prepare chemical solutions for products and processes using standardized formulas, and develop experimental formulations as needed for research and development projects.</li><li>Maintain, clean, and sterilize laboratory instruments, equipment, and work areas to ensure safe and efficient operations.</li><li>Write technical reports and prepare graphs, charts, and other visual documentation to communicate experimental methods, results, and conclusions.</li><li>Order, track, and inventory laboratory materials, chemicals, and supplies to maintain appropriate stock levels and support continuous laboratory operations.</li><li>Collaborate with cross-functional teams to support quality assurance, analytical chemistry, and wet chemistry testing related to product development and quality control.</li><li>Perform accurate data entry and documentation in laboratory information systems and spreadsheets to support traceability and compliance requirements.</li></ul>Essential Skills<ul><li>Associate’s degree in applied science or a related field required.</li><li>Bachelor’s degree in Chemistry or Biology preferred, with strong consideration for similar academic backgrounds such as Biochemistry or Chemical Engineering.</li><li>0–2 years of experience in a laboratory, analytical chemistry, wet chemistry, quality assurance, or quality control environment.</li><li>Basic knowledge of chemical composition, structure, and properties of substances, and the chemical processes and transformations they undergo.</li><li>Basic understanding of chemical manufacturing processes and how they affect the environment, as well as worker and consumer safety.</li><li>Demonstrated creativity in approaching laboratory tasks and problem solving.</li><li>Strong verbal and written communication skills to document and present experimental work clearly.</li><li>Solid analytical and problem-solving skills, with the ability to interpret complex data and troubleshoot issues in experiments or processes.</li><li>Ability to multi-task and manage numerous projects or experiments simultaneously while meeting deadlines.</li><li>High attention to detail, with a track record of accurate work and thorough documentation.</li><li>Familiarity with MS Office applications for data entry, analysis, and reporting.</li><li>Comfort working with laboratory equipment and techniques such as chromatography, spectroscopy, separation techniques, microscopy, and standard analytical chemistry methods.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor of Science degree in Chemistry, Biology, Biochemistry, Chemical Engineering, or a closely related scientific discipline is preferred.</li><li>Experience in analytical chemistry, wet chemistry, and laboratory-based quality assurance or quality control is beneficial.</li><li>Familiarity with statistical software and tools for data analysis is preferred.</li><li>Experience with data entry and documentation in laboratory or quality systems is an advantage.</li><li>Ability to work effectively as a team player in a collaborative laboratory environment.</li><li>Demonstrated ability to adapt to new methods, technologies, and projects as training and development opportunities arise.</li><li>Interest in long-term professional growth within a science- and technology-driven organization.</li></ul>Work EnvironmentThis position is 100% onsite at a modern laboratory and campus-based facility and is not open to remote work. The standard schedule is Monday through Friday, 8:00 a.m. to 4:30 p.m., with some flexibility as needed. The campus features a pleasant environment with a walking path surrounding the facility, providing opportunities to take breaks outdoors. An on-site cafeteria offers a variety of food options and an outdoor terrace where you can enjoy lunch outside. You will work in a laboratory setting that supports research, development, and quality control activities, using core technologies such as analytical chemistry, wet chemistry, chromatography, spectroscopy, and related laboratory equipment. The broader organization focuses on water, hygiene, and infection prevention solutions and services, with a large team of scientists, engineers, and technical specialists developing solutions that consider human health and environmental impact. Consultants and new team members receive training and integration support, and those who perform well may have opportunities to move into other projects and network with other groups for longer-term roles. Appropriate laboratory attire and safety practices are required in the lab environment.Job Type &amp; LocationThis is a Contract to Hire position based out of EAGAN, MN.Pay and BenefitsThe pay range for this position is $21.00 - $22.00/hr.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 EAGAN,MN.Application DeadlineThis position is anticipated to close on Aug 3, 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.

Lab TechnicianJob DescriptionThe Lab Technician is responsible for performing daily evaluations and approvals of finished products, conducting process quality checks, and executing basic microbiological testing. The role includes equipment calibration, troubleshooting, and dilution calculations. This position involves conducting ingredient and packaging inspections, maintaining inventory control, and managing sample archives. The Lab Technician will perform laboratory tests, including solvent extraction, sieving, pH, protein, fiber, fat, ash, and microbiological plating, as well as testing raw ingredients and finished packaged products. Test results must be recorded accurately, and communication with operating departments and management is essential. The role requires performing in-process quality checks, collecting test samples, troubleshooting equipment, and performing mechanical maintenance. A clean, safe work environment is maintained through general lab clean-up, and tasks are performed with minimal supervision.Responsibilities<ul><li>Perform daily evaluations and approvals of finished products.</li><li>Conduct process quality checks and basic microbiological testing.</li><li>Calibrate equipment, troubleshoot issues, and calculate dilutions.</li><li>Conduct ingredient and packaging inspections and maintain inventory control.</li><li>Manage sample archives and perform laboratory tests.</li><li>Record test results and communicate findings to relevant departments.</li><li>Perform in-process quality checks and collect test samples.</li><li>Troubleshoot equipment and perform mechanical maintenance.</li><li>Maintain a clean and safe laboratory work environment.</li></ul>Essential Skills<ul><li>0-2 years of laboratory experience.</li><li>Basic wet chemistry knowledge.</li><li>Scientific mindset with a degree in chemistry or biology.</li><li>Experience with lab testing, wet chemistry, pH testing, and sample testing.</li></ul>Additional Skills &amp; Qualifications<ul><li>Interest in working in a food facility.</li><li>Manufacturing experience is a plus.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Saint Joseph, MO.Pay and BenefitsThe pay range for this position is $19.00 - $19.00/hr.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 Saint Joseph,MO.Application DeadlineThis position is anticipated to close on Aug 4, 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 DescriptionAs a Lab Technician, you will assist in applications development by preparing samples, performing analytical tests, recording data and observations, and preparing summaries of experiments. You will be involved in both manual and automated die bonding applications, troubleshooting basic process issues, and performing parameter optimization and failure analysis.Responsibilities<ul><li>Assist in applications development by preparing samples and performing analytical tests.</li><li>Record data and observations, and prepare summaries of experiments.</li><li>Perform die bonding applications both manually and with automation.</li><li>Troubleshoot basic process issues and escalate them appropriately.</li><li>Perform parameter optimization and failure analysis.</li><li>Handle microscopic components using microscopes, tweezers, and vacuum tools.</li><li>Document processes, perform basic troubleshooting, and maintain repeatability and yield.</li></ul>Essential Skills<ul><li>B.S. In Materials Science, Chemistry, or related field</li><li>1+ years of industry experience in Material Sciences or related field</li><li>Experience in materials testing, working with metals, QC, or lab experience.</li><li>Basic computer skills, including Microsoft Excel, Word, and PowerPoint.</li><li>Ability to log process data and familiarity with statistical analysis software such as Minitab.</li><li>Ability to work in a team environment, follow instructions, and communicate effectively.</li><li>Hands-on approach with good time management skills.</li><li>Strong attention to detail with a focus on process control, documentation, and maintaining quality.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with statistical analysis software such as Minitab is a plus.</li><li>Ability to stand, reach, and use fine tools.</li><li>Occasionally lift small weights or handle assemblies.</li></ul>Work EnvironmentWork in a lab environment that offers a small company feel with big financial backing. Experience a great culture where everyone gets along and is supportive.Job Type &amp; LocationThis is a Contract to Hire position based out of San Jose, CA.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr.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 San Jose,CA.Application DeadlineThis position is anticipated to close on Aug 5, 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: Lab TechnicianJob DescriptionThe Lab Technician will prepare and analyze food-related samples using wet chemistry techniques to support the production of vitamin and mineral premixes and specialty enzyme-based ingredient blends. This role focuses on testing raw materials and finished goods, generating precise and reliable analytical data, maintaining laboratory instruments, and ensuring compliance with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards. Responsibilities<ul><li>Prepare and process food samples for analysis, primarily using wet chemistry methods such as pH measurements, titrations, and acid–base preparations.</li><li>Perform routine laboratory tasks competently and independently, including weighing, pipetting, and volumetric dilutions for sample preparation.</li><li>Conduct wet chemistry tests on raw materials and finished goods to support quality control of vitamin/mineral blends, premixes, and specialty food ingredients.</li><li>Generate precise, reliable, and reproducible analytical data in a timely manner to support production and quality assurance needs.</li><li>Troubleshoot experiments and laboratory instrumentation to resolve issues and maintain data integrity.</li><li>Maintain instrument calibration and ensure equipment is functioning properly according to laboratory standards.</li><li>Learn and eventually operate ICP-MS instrumentation, following established methods and procedures.</li><li>Handle analytical instruments such as HPLC and other related equipment as needed to support laboratory testing.</li><li>Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials and controlled compounds, and GMP compliance where applicable.</li><li>Comply with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) requirements in daily laboratory activities.</li><li>Perform general laboratory housekeeping, including cleaning, disinfecting, sweeping, mopping, organizing, and maintaining the overall aesthetics of the lab.</li><li>Collaborate with production and other internal teams by communicating test results and supporting ongoing projects.</li><li>Perform other related laboratory duties as assigned to support the growth and development of the lab.</li></ul>Essential Skills<ul><li>Hands-on wet chemistry experience, including pH measurement, titrations, and acid–base preparation.</li><li>Ability to perform sample preparation techniques such as weighing, pipetting, and volumetric dilutions with high accuracy.</li><li>Analytical laboratory experience with instruments such as HPLC, ICP, ICP-MS, AA, or similar analytical technologies.</li><li>Understanding and practical application of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).</li><li>Capability to work alone and independently without direct supervision while maintaining high standards of quality and safety.</li><li>Strong interpersonal and organizational skills to manage multiple tasks and interact effectively with team members.</li><li>Clear and effective communication skills, both verbal and written, for reporting data and collaborating with others.</li><li>Responsive problem-solving skills and an action-oriented mindset to address laboratory challenges quickly and effectively.</li><li>Proficiency in Microsoft Office, including Microsoft Excel, for data entry, manipulation, and basic analysis.</li><li>1–2 years of laboratory experience, preferably with analytical laboratory exposure.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in a scientific field (such as chemistry, biochemistry, or related sciences) is beneficial.</li><li>Experience working in food, beverage, or related ingredient manufacturing environments is an advantage.</li><li>Experience in quality control testing for raw materials and finished goods is preferred.</li><li>Familiarity with high-performance liquid chromatography (HPLC) and other analytical instruments used in chemical analysis.</li><li>Comfort working as the first dedicated laboratory hire and interest in growing into a lab lead or manager role as the lab expands.</li><li>Ability to collaborate with production teams and administrative staff in a small, closely knit organization.</li><li>Strong attention to detail and commitment to generating accurate and reproducible analytical data.</li></ul>Work EnvironmentThe position is a first-shift schedule typically running from 8:30 a.m. to 4:30 p.m., Monday through Friday. The work involves regular use of wet chemistry techniques and analytical instruments such as HPLC and ICP-MS, with a strong emphasis on GMP and GLP compliance, safety, and cleanliness. The laboratory environment requires comfort working independently, maintaining a high level of organization, and upholding a professional, neat appearance appropriate for a food-related manufacturing and quality control setting.Job Type &amp; LocationThis is a Contract to Hire position based out of Glendale Heights, IL.Pay and BenefitsThe pay range for this position is $23.00 - $30.00/hr.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 Glendale Heights,IL.Application DeadlineThis position is anticipated to close on Aug 3, 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.

Actively Screening for Lab Assistant to join top medical laboratory in Norcross, GA!Job DescriptionAs a Lab Assistant, you will be responsible for performing various duties assigned by the department, maintaining accurate records and documentation, recognizing unusual results and resolving discrepancies, and communicating unusual occurrences to management.Responsibilities<ul><li>Perform SATR.</li><li>Operate P512.</li><li>Receive and sort boxes.</li><li>Sort samples.</li><li>Operate IDETIC as assigned.</li><li>Conduct sample investigations.</li><li>Dispose of biohazard materials.</li></ul>Essential Skills<ul><li>Experience in laboratory settings.</li><li>Proficient in sample handling and accessioning.</li><li>Ability to conduct data entry efficiently.</li><li>Knowledge of inventory management, SOP, and quality control.</li></ul>Work EnvironmentWarehouse and laboratory environment Lab Assistant | Day shift (Sunday-Wednesday)Regular Schedule: Sunday–Wednesday, 7:00 AM – 5:30 PMTraining Schedule: Sunday–Tuesday: 10:00 AM – 10:30 PM (training schedule may change depending on needs)Job Type &amp; LocationThis is a Contract position based out of Norcross, GA.Pay and BenefitsThe pay range for this position is $18.00 - $18.00/hr.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 Norcross,GA.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Lab Technician We are seeking a detail-oriented and motivated Laboratory Technician II to support laboratory testing, quality control, and analytical activities in a fast-paced environment. This role is responsible for performing routine and non-routine laboratory analyses, maintaining accurate records, operating laboratory equipment, and ensuring compliance with company procedures, quality standards, and safety requirements. The ideal candidate will have at least 2–5 years of laboratory experience and be comfortable working independently while collaborating with cross-functional teams.<h2>Key Responsibilities</h2><ul><li>Perform chemical, biological, physical, or quality control testing according to established methods and procedures.</li><li>Prepare samples, reagents, standards, and solutions for laboratory analyses.</li><li>Operate, calibrate, troubleshoot, and maintain laboratory instrumentation and equipment.</li><li>Record, analyze, and report test results accurately and in a timely manner.</li><li>Review data for accuracy and investigate out-of-specification or unusual results.</li><li>Maintain laboratory notebooks, electronic records, and documentation in accordance with quality standards.</li><li>Assist with method validation, process improvement initiatives, and laboratory investigations.</li><li>Ensure compliance with GMP, GLP, ISO, FDA, EPA, OSHA, or other applicable regulations.</li><li>Monitor inventory levels and assist with ordering laboratory supplies and materials.</li><li>Support audits, inspections, and quality assurance activities.</li><li>Participate in training and mentor junior laboratory staff when needed.</li><li>Follow all laboratory safety procedures and maintain a clean, organized work environment.</li></ul><h2>Qualifications</h2><ul><li>Associate's or Bachelor's degree in Chemistry, Biology, Microbiology, Biochemistry, Environmental Science, or a related scientific field.</li><li>1-3 years of laboratory experience in an industrial, environmental, pharmaceutical, food &amp; beverage, manufacturing, or research setting.</li><li>Experience performing laboratory testing and maintaining detailed documentation.</li><li>Strong attention to detail and organizational skills.</li><li>Proficient with Microsoft Office applications and laboratory data systems.</li></ul><h3>Preferred</h3><ul><li>Experience with analytical instrumentation such as HPLC, GC, ICP, UV-Vis, FTIR, or other laboratory equipment.</li><li>Knowledge of GMP, GLP, ISO, or other regulated laboratory environments.</li><li>Previous experience troubleshooting laboratory issues and investigating non-conforming results.</li></ul><h2>Knowledge, Skills, and Abilities</h2><ul><li>Strong analytical and problem-solving skills.</li><li>Ability to prioritize tasks and manage multiple projects simultaneously.</li><li>Excellent written and verbal communication skills.</li><li>Ability to work independently with minimal supervision.</li><li>Commitment to quality, safety, and continuous improvement.</li></ul><h2>Physical Requirements</h2><ul><li>Ability to stand for extended periods.</li><li>Ability to lift up to 25 pounds occasionally.</li><li>Ability to work around laboratory chemicals, equipment, and industrial environments while following all safety protocols.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Louisville, KY.Pay and BenefitsThe pay range for this position is $24.00 - $24.00/hr.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 Louisville,KY.Application DeadlineThis position is anticipated to close on Jul 31, 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.

Laboratory Technician – Gas AnalysisJob DescriptionThe Laboratory Technician – Gas Analysis works in one of several analytical laboratories performing routine and non‑routine analysis of medical and specialty gases to detect impurities and verify product quality. This hands‑on role involves operating analytical instrumentation, connecting and handling gas cylinders, using laboratory software, and maintaining strict adherence to quality, safety, and regulatory requirements. The position offers the opportunity to support a growing industry with strong potential for long‑term career growth and conversion to a permanent role.Responsibilities<ul><li>Perform analytical testing of gas samples for impurities using gas chromatography and spectroscopic techniques to verify product quality.</li><li>Connect gas cylinders to analytical systems within ventilated cabinets, initiate analysis runs, and safely disconnect cylinders upon completion, with cylinder hook‑up and removal potentially taking up to 30 minutes per sample.</li><li>Operate and maintain gas chromatography systems, including GC and GCP‑type instruments, using Galaxy/Compass GC control software to conduct precise analyses.</li><li>Utilize Fourier Transform Infrared (FTIR) spectrometers to identify and quantify gas components and trace impurities.</li><li>Conduct analysis using CO₂ analyzers to measure carbon dioxide concentration and purity as required by product specifications.</li><li>Upload, review, and document analytical results in the Laboratory Information Management System (LIMS) to ensure accurate data capture and traceability.</li><li>Perform routine calibration, verification, and basic maintenance of analytical instruments to maintain accuracy, reliability, and regulatory compliance.</li><li>Analyze finished gas products to confirm purity and conformance to internal specifications and customer requirements.</li><li>Calculate, prepare, and fill medical and specialty gas mixtures and pure gases using partial pressure and gravimetric techniques.</li><li>Test and certify incoming raw materials prior to use in production to ensure they meet required standards.</li><li>Process cylinders for shipment, including painting, labeling, valve preparation, and generating certificates of analysis.</li><li>Maintain complete and accurate quality control records and documentation in compliance with company policies and applicable local, state, and federal regulations.</li><li>Handle, move, and load gas cylinders as required to support testing, production, and shipment activities.</li><li>Participate in all required safety training and activities, and actively maintain a safe, compliant laboratory work environment.</li><li>Apply knowledge of chromatographic peak characteristics and instrument control to interpret results and troubleshoot analyses as needed.</li></ul>Essential Skills<ul><li>Experience working in a laboratory environment with a focus on chemistry, quality control, and analytical testing.</li><li>Hands‑on experience with gas chromatography techniques and chromatographic analysis.</li><li>Ability to operate GC and GCP‑type systems and use GC controlling software such as Galaxy/Compass for instrument control and data acquisition.</li><li>Understanding of chromatographic peak characteristics and related data interpretation.</li><li>Familiarity with spectroscopic techniques, including Fourier Transform Infrared (FTIR) spectroscopy, for gas analysis.</li><li>Experience handling toxic and hazardous chemicals in a controlled laboratory setting, following established safety protocols.</li><li>Knowledge of gas handling systems, ventilated cabinets, and safe cylinder connection, disconnection, and movement.</li><li>Ability to perform routine calibration, verification, and basic maintenance of analytical instruments.</li><li>Competence in using a Laboratory Information Management System (LIMS) for uploading, reviewing, and documenting analytical results.</li><li>Strong attention to detail and commitment to maintaining complete and accurate quality control records in compliance with regulatory requirements.</li><li>Ability to calculate, prepare, and fill gas mixtures using partial pressure and gravimetric techniques.</li><li>Capability to work rotating day and night shifts, including weekends and holidays, in a 24/7 operational environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Chemistry or Chemical Engineering, OR at least 2 years of analytical laboratory experience.</li><li>Toxic chemical handling experience preferred, including safe work practices and hazard awareness.</li><li>Open to entry‑level graduates with chemical handling experience gained through academic laboratory work or internships.</li><li>Background in Good Manufacturing Practice (GMP) or regulated laboratory environments is beneficial.</li><li>Experience as a laboratory technician or chemical engineer in analysis‑focused roles is an advantage.</li><li>Familiarity with concepts related to chromatographic order and peak behavior to support method execution and troubleshooting.</li><li>Ability to work accurately under time constraints while managing multiple samples and tasks.</li><li>Strong communication skills to document results clearly and collaborate with laboratory and production teams.</li><li>Interest in long‑term growth within a rapidly expanding industry, with potential for conversion from consulting to permanent employment.</li><li>Reliability and flexibility to adhere to a structured rotating schedule and maintain consistent performance across day and night shifts.</li></ul>Work EnvironmentThe role is based in a very clean and organized chemistry laboratory dedicated to medical and specialty gas analysis. The environment involves frequent handling of gas cylinders and extremely hazardous chemicals, requiring strict adherence to safety procedures, use of appropriate personal protective equipment, and compliance with regulatory standards. Laboratory equipment includes gas chromatography systems (GC and GCP‑type), Galaxy/Compass GC control software, Fourier Transform Infrared (FTIR) spectrometers, CO₂ analyzers, gas handling systems, ventilated cabinets, and a Laboratory Information Management System (LIMS). The position follows a DuPont rotating schedule that provides 24/7 operational coverage, with structured rotations between day and night shifts. The schedule includes weekends and holidays based on the rotation rather than a traditional Monday–Friday pattern, and is published well in advance, offering longer stretches of time off compared to a standard workweek. The role offers 8 paid holidays and a vacation/PTO structure where consultants receive 40 hours of PTO for every 6 months of tenure, along with the opportunity to transition to a permanent position in a growing industry.Job Type &amp; LocationThis is a Contract to Hire position based out of Waverly, TN.Pay and BenefitsThe pay range for this position is $28.00 - $28.00/hr.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 Waverly,TN.Application DeadlineThis position is anticipated to close on Jul 31, 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: Lab Technician Job DescriptionThis Lab Technician role combines hands-on laboratory work with active involvement on the production floor in an industrial plating and manufacturing environment. You will support lab waste treatment, perform basic wet chemistry and titration testing, and analyze how changes in chemistry impact product quality and process performance. This position is ideal for someone who enjoys process improvement, wants to grow long term, and is comfortable working both in the lab and in a fast-paced, industrial setting rather than a traditional "white lab coat" research lab.Responsibilities<ul><li>Operate and support the waste treatment facility, ensuring safe and compliant handling of process waste streams.</li><li>Perform basic wet chemistry, including titrations, pH testing and adjustment, metal precipitation, and polymer dosing and pumping.</li><li>Analyze chemistry test results and determine appropriate bath and process adjustments to maintain optimal performance and product quality.</li><li>Communicate clear, actionable recommendations to production staff based on laboratory findings and process analysis.</li><li>Regularly walk the production floor to observe product quality, monitor process performance, and connect lab results to real-time operations.</li><li>Identify opportunities for process improvements by linking chemical conditions to production outcomes and recommending changes.</li><li>Partner with internal teams and external chemical supplier representatives to analyze data and optimize plating and finishing processes.</li><li>Support quality control and quality assurance activities by providing timely and accurate lab data and documentation.</li><li>Contribute to continuous improvement initiatives by suggesting and helping implement changes that enhance efficiency, consistency, and product performance.</li><li>Develop a deeper understanding of the production side over time, expanding from lab and waste treatment responsibilities into broader process improvement work.</li><li>Take an active, hands-on role in learning new tools, techniques, and equipment used in plating, finishing, and chemical process operations.</li><li>Grow into higher-level responsibilities as your skills and understanding of the processes and facility increase.</li></ul>Essential Skills<ul><li>Experience working as a lab technician, in waste treatment, plating, process technician roles, or in a similar industrial or laboratory environment.</li><li>Basic chemistry knowledge with the ability to perform and interpret wet chemistry tests and titrations.</li><li>Strong interest in process improvement and a desire to use data and observations to enhance product quality and process performance.</li><li>Comfort working in an industrial manufacturing setting, not solely in a traditional laboratory environment.</li><li>Effective communication skills to explain findings and recommendations to production staff and other stakeholders.</li><li>Critical thinking and problem-solving skills to connect lab data, process conditions, and production outcomes.</li><li>Willingness to work in a hands-on capacity and spend meaningful time on the production floor.</li><li>Openness to learning and training, with the mindset and aptitude to grow from a more junior level into broader responsibilities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Exposure to atomic absorption, x-ray measurement, or similar analytical tools.</li><li>Experience in metal finishing, plating, or chemical process operations.</li><li>Chemistry education or coursework is preferred, particularly for candidates interested in applying practical chemistry in an industrial environment.</li><li>Balanced interest in applied, hands-on work rather than purely research-focused roles.</li><li>Motivation to build a long-term career with opportunities to expand from lab and waste treatment into process optimization and continuous improvement.</li><li>Hands-on, proactive approach and genuine interest in learning the production side of the operation.</li><li>Capacity to grow into higher-level responsibilities as skills, knowledge, and experience develop over time.</li></ul>Work EnvironmentThis role is based in an industrial plating and manufacturing environment rather than a traditional office or research lab. You will split your time between the lab and the production floor, performing basic chemistry analysis and then walking the floor to observe product quality and monitor how process changes impact output. The workday schedule is Monday through Friday, approximately 7:00 a.m. to 4:00 p.m., and the environment is hands-on, fast-paced, and collaborative. You will interact regularly with lab staff, production employees, facility leadership, and outside chemical representatives. The setting involves typical industrial conditions, including active production lines and plating operations, and is best suited to someone who is comfortable being visible on the floor, wearing appropriate industrial attire and protective equipment, and playing an active role in improving processes rather than remaining solely at the lab bench.Job Type &amp; LocationThis is a Contract position based out of Ypsilanti, MI.Pay and BenefitsThe pay range for this position is $20.00 - $27.00/hr.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 Ypsilanti,MI.Application DeadlineThis position is anticipated to close on Jul 28, 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: Lab TechnicianJob DescriptionThe Lab Technician performs a wide range of laboratory tests and quality assurance activities to ensure materials and processes meet required specifications. This role focuses on setting up and running physical, chemical, and environmental tests, accurately recording and analyzing data, maintaining laboratory equipment, and supporting material control in a fast-paced manufacturing environment.Responsibilities<ul><li>Set up and perform government tests such as climbing drum peels and lap shears, including preparing specimens, configuring machines and chart recorders, running tests, reading results, and entering data into the computer.</li><li>Conduct flame tests by setting up test equipment, identifying specimens, running the tests, measuring results, and recording all data accurately in the computer.</li><li>Perform 168-hour tests by preparing samples, setting up equipment and chart recorders, running tests to completion, and entering results into the appropriate electronic worksheets.</li><li>Measure airborne particles in layup and prime rooms, calculate average readings, and enter results into the computer for ongoing environmental monitoring.</li><li>Monitor solution temperatures and water purity by taking readings of rinse water, recording results, and documenting tank temperatures in the computer.</li><li>Monitor and record temperature, humidity, and pressure differential in prime and layup rooms, and change and store charts from the lab, layup, and prime areas.</li><li>Perform solution analysis by testing aluminum and acid concentrations in deoxidizing and anodizing tanks and alkaline concentration in cleaner tanks, including preparing beakers, collecting samples, calibrating and maintaining pH and aluminum meters, running tests, and recording results in computerized charts.</li><li>Communicate test findings and required adjustments to process operators and ensure proper cleanup and storage of equipment and chemicals after solution analysis.</li><li>Conduct material testing for initial inspection and revalidation to verify conformance to specifications, including tests such as visual inspection, resin content, volatile content, gel time, flow, tack, lap shear, T-peel, thickness, expansion, density, hardness, compression strength, viscosity, and pot life.</li><li>Manage material control for time- and temperature-sensitive materials by tracking expiration dates, remaining shelf life, in-time and out-time, and maintaining inventory of kits and materials in freezers, the lab, layup room, prime room, and shop floor.</li><li>Issue weekly wedge crack test travelers to the appropriate processing line, record received results, and maintain automated reports that summarize averages and test outcomes.</li><li>Perform general laboratory support activities including inventorying, ordering, and stocking lab supplies, maintaining and cleaning equipment, and keeping the lab clean and organized.</li><li>Check certifications of received goods, issue test travelers, print labels, inventory expired products, and file and organize certifications, purchase orders, and test documentation.</li><li>Use gauges, measuring equipment, and other detection methods to verify product conformance to specifications.</li><li>Maintain the integrity of the Quality Management System at all times in relation to quality assurance processes and documentation.</li><li>Work independently to meet commitments, adapt to changes, manage workload effectively, and maintain reliable attendance and punctuality.</li></ul>Essential Skills<ul><li>High school diploma or GED.</li><li>At least 1 year of experience in an inspection environment.</li><li>Ability to read and comprehend simple instructions, short correspondence, and memos.</li><li>Ability to write clear and simple correspondence and present information effectively in one-on-one and small group settings.</li><li>Ability to solve practical problems and work with a variety of concrete variables where limited standardization exists.</li><li>Ability to interpret written, oral, diagram, and schedule instructions and apply common sense understanding to carry out tasks.</li><li>Ability to deal with problems involving several concrete variables in standardized situations.</li><li>Strong organizational skills and the ability to understand and follow technical specifications.</li><li>Basic understanding of material management and material testing processes.</li><li>Ability to use gauges, measuring equipment, and detection methods to confirm product conformance.</li><li>Proficiency with spreadsheet and word processing software, including Excel and word processing applications.</li><li>Ability to meet commitments, work independently, accept accountability, handle changes, maintain focus under pressure, and meet attendance and punctuality expectations.</li><li>Eligibility to meet Export Control compliance requirements as a US Person as defined by 22 C.F.R. §120.15.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in a technology or science-based field is preferred.</li><li>Direct composite testing experience of at least 1–3 years is preferred.</li><li>Knowledge of Epicor or similar ERP software is preferred.</li><li>Experience with laboratory quality assurance and quality control practices.</li><li>Familiarity with chemistry-related lab work such as titration and solution analysis.</li><li>Experience with techniques such as HPLC is beneficial but not required.</li></ul>Work EnvironmentThis role is based 100% in a manufacturing area and follows a Monday–Friday schedule, typically 7:00 a.m.–4:00 p.m. or 8:00 a.m.–5:00 p.m. The environment includes moderate noise levels and frequent work near moving mechanical parts, approximately 90% of the time. The position involves exposure to fumes or airborne particles about 50% of the time. Work is performed in and around laboratory, layup, prime, and shop floor areas with process equipment, test machines, and computer systems. Appropriate personal protective equipment is provided and required as needed for safe operation in a production and lab setting.If you are interested please book a virtual meeting with me through this link: https://talentassistant.actalentservices.com/assistant/bookings/bgF9HVktJob Type &amp; LocationThis is a Contract to Hire position based out of Berlin, CT.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.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 Berlin,CT.Application DeadlineThis position is anticipated to close on Jul 27, 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.

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