Actalent
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QA Technical Writer
role at
Actalent .
Responsibilities
Draft and review Laboratory Investigation Reports (LIRs) in response to laboratory deviations, OOS results, and non-conformances.
Collaborate with analysts, QA, and SMEs to gather data and ensure accurate documentation.
Conduct root cause analysis and document corrective and preventive actions (CAPAs).
Ensure LIRs meet regulatory and internal standards (FDA, cGMP, ICH).
Qualifications
Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biochemistry).
2+ years of experience in a GMP-regulated lab or QA environment.
Experience writing Laboratory Investigation Reports (LIRs).
Strong understanding of laboratory operations, OOS investigations, and CAPA processes.
Key Skills Technical writing, GMP.
Experience Level Intermediate Level.
Job Type & Location Contract position based in Vernon Hills, IL.
Workplace Type Fully onsite position.
Pay and Benefits The pay range for this position is $31.00 - $36.00/hr.
Benefits may include:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) retirement plan – Pre‑tax and Roth post‑tax contributions available
Life insurance (Voluntary Life & AD&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)
Application Deadline This position is anticipated to close on Nov 14, 2025.
About Actalent Actalent is a global leader in engineering and science 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
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QA Technical Writer
role at
Actalent .
Responsibilities
Draft and review Laboratory Investigation Reports (LIRs) in response to laboratory deviations, OOS results, and non-conformances.
Collaborate with analysts, QA, and SMEs to gather data and ensure accurate documentation.
Conduct root cause analysis and document corrective and preventive actions (CAPAs).
Ensure LIRs meet regulatory and internal standards (FDA, cGMP, ICH).
Qualifications
Bachelor’s degree in a scientific discipline (e.g., Chemistry, Biology, Biochemistry).
2+ years of experience in a GMP-regulated lab or QA environment.
Experience writing Laboratory Investigation Reports (LIRs).
Strong understanding of laboratory operations, OOS investigations, and CAPA processes.
Key Skills Technical writing, GMP.
Experience Level Intermediate Level.
Job Type & Location Contract position based in Vernon Hills, IL.
Workplace Type Fully onsite position.
Pay and Benefits The pay range for this position is $31.00 - $36.00/hr.
Benefits may include:
Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) retirement plan – Pre‑tax and Roth post‑tax contributions available
Life insurance (Voluntary Life & AD&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)
Application Deadline This position is anticipated to close on Nov 14, 2025.
About Actalent Actalent is a global leader in engineering and science 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
#J-18808-Ljbffr