We are looking to add a position to help support a Gene Therapy Laboratory here in Columbus! This role will primarily be handling a lot of the regulatory documentation for the lab, and will not be working in the lab itself. This is a great opportunity for someone who wants to continue to growing in the sciences, but isn't necessarily set on being in a lab environment.

An ideal candidate will come from a heavily regulated environment where they had to perform a lot of documentation, which could include working in a laboratory or in a regulatory or quality documentation environment. The experience must be heavily regulated - relevant industries may include, but are not limited to: Pharmaceuticals, Gene Therapy, Cosmetics, Food, etc. Relevant regulations may include, but are not limited to: GMP, GLP, FDA, etc.

Job Description

The Document Control Technician will play a critical role in supporting clinical and commercial programs at our 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 that documentation is maintained following internal procedures and regulatory standards.

Qualifications

BS or Associate's in a Science and industry experience in a heavily regulated environment.Prior experience with document controlExperience working with GMP or FDA regulations is strongly preferred

Pay and Benefits

The pay range for this position is $22.00 - $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 & 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 Sep 19, 2025.

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.