Actalent
We are looking to add a Quality Specialist II with a large Gene Therapy company in the area!
This team serves as the first line of defense for whenever there's any issues in the suite/lab and some guidance might be needed.
This role handles all quality documentation and concerns before determining if an issue might need to be escalated to the Investigations team. This role does not perform any laboratory testing, and focuses more on the documentation side of things.
An ideal candidate will have a Bachelors in a science and at least 2-3+ years of experience working in a heavily regulated quality laboratory or documentation environment. Experience can come from GMP, GLP, FDA, or other similarly regulated environments where you had to follow Good Documentation Practices (typically anything in food or pharma would qualify). This is a 1st shift opportunity.
Description This is the largest part of the quality team and provides the first line of defense whenever any issues pop up in the laboratory. This role may involve going into the cleanroom about twice a week, but does not perform any laboratory testing. Job duties will primarily include:
Reviewing any discrepancies to see if they can be remedied, or if they need to be escalated.
Review batch records.
Oversee and assist with any guidance needed in the cleanroom.
Perform various quality documentation.
Review quality documentation to ensure it meets necessary regulations and guidelines.
Qualifications
Must have a Bachelors Degree (preferably in a scientific field)
Must have at least 2-3+ years of experience working in the quality department in a heavily regulated environment (GMP preferred, but would also consider GLP, FDA, or other similarly regulated environments). Must have strong documentation experience.
Job Type & Location This is a Permanent position based out of Columbus, OH.
Pay and Benefits The pay range for this position is $28.00 - $28.00/hr.
If eligible, the benefits available for this role may include the following:
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)
Workplace Type This is a fully onsite position in Columbus, OH.
Application Deadline This position is anticipated to close on Jan 19, 2026.
About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 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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This role handles all quality documentation and concerns before determining if an issue might need to be escalated to the Investigations team. This role does not perform any laboratory testing, and focuses more on the documentation side of things.
An ideal candidate will have a Bachelors in a science and at least 2-3+ years of experience working in a heavily regulated quality laboratory or documentation environment. Experience can come from GMP, GLP, FDA, or other similarly regulated environments where you had to follow Good Documentation Practices (typically anything in food or pharma would qualify). This is a 1st shift opportunity.
Description This is the largest part of the quality team and provides the first line of defense whenever any issues pop up in the laboratory. This role may involve going into the cleanroom about twice a week, but does not perform any laboratory testing. Job duties will primarily include:
Reviewing any discrepancies to see if they can be remedied, or if they need to be escalated.
Review batch records.
Oversee and assist with any guidance needed in the cleanroom.
Perform various quality documentation.
Review quality documentation to ensure it meets necessary regulations and guidelines.
Qualifications
Must have a Bachelors Degree (preferably in a scientific field)
Must have at least 2-3+ years of experience working in the quality department in a heavily regulated environment (GMP preferred, but would also consider GLP, FDA, or other similarly regulated environments). Must have strong documentation experience.
Job Type & Location This is a Permanent position based out of Columbus, OH.
Pay and Benefits The pay range for this position is $28.00 - $28.00/hr.
If eligible, the benefits available for this role may include the following:
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)
Workplace Type This is a fully onsite position in Columbus, OH.
Application Deadline This position is anticipated to close on Jan 19, 2026.
About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 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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