Quality Technician

QA Document Control Technician

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH  OR TEXT MARISA . 1302 TO SET UP A PHONE INTERVIEW!

This position is fully documentation with no lab work

The QA Document Control Technician will play a critical role in clinical and commercial programs at a biosciences GMP manufacturing facility. This position will be responsible for managing the creation, revision, storage, and retrieval of all controlled documentation in accordance with GMP regulations and internal quality systems. The technician will ensure that documentation practices comply with regulatory standards while supporting continuous improvement initiatives in manufacturing processes.

• Perform essential Document Control functions in a timely manner to support the efficient functioning of the Manufacturing Facility.

• Register controlled documents, monitor and communicate revision and review cycles, and issue production documents.

• Assist with organizing and maintaining the QA Documents Room by scanning, filing, and archiving GMP records.

• Ensure documentation is maintained following internal procedures and regulatory requirements.

• Move paper boxes and files as necessary.

• Bachelors or Associate's degree in science preferred, or high school diploma with 2+ years of industry experience.

• Prior experience with document control.

• Experience working with GMP or FDA regulations is strongly preferred.

• Understanding of regulatory and documentation constraints in a GMP environment.

• Great communication and writing skills required.

• Proficiency with Word and Excel.

This rapidly growing company is expanding its operations with two new sites in Columbus, Ohio, featuring state-of-the-art clean rooms and equipment. The position involves working in cross-functional teams in a modern and dynamic environment.

1st shift M-F 9am-5:30pm (Must have some flexibility to come in earlier or leave later)

This is a Contract to Hire position based out of Columbus, OH.

The pay range for this position is $22.00 - $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 & 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-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Columbus,OH.

This position is anticipated to close on Jan 11, 2026.

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 actalentaccom (%20actalentaccom) for other accommodation options.