What are the responsibilities and job description for the GMP Documentation Technician position at Actalent?
Job Title: GMP Documentation TechnicianJob 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.
Responsibilities
This is a quickly growing new company breaking off from NCH, currently building two new sites in Columbus, Ohio. The facility includes state-of-the-art clean rooms and equipment. Employees will work in cross-functional teams in a rapidly evolving environment.
Job Type & Location
This is a Contract to Hire position based out of Columbus, OH.
Pay And Benefits
The pay range for this position is $26.00 - $27.50/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:
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.
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.
Responsibilities
- Perform essential Document Control functions in a timely manner to support the efficient functioning of the Manufacturing Facility.
- Register controlled documents and monitor and communicate revision and review cycles.
- Issue production documents and 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 guidelines.
- BS or associate's degree in science preferred or a high school diploma with 2 years of industry experience.
- Prior experience with document control.
- Experience working with GMP or FDA regulations is strongly preferred.
- Great communication and writing skills required.
- Proficiency with Word and Excel.
- Understanding of regulatory and documentation constraints in a GMP environment.
This is a quickly growing new company breaking off from NCH, currently building two new sites in Columbus, Ohio. The facility includes state-of-the-art clean rooms and equipment. Employees will work in cross-functional teams in a rapidly evolving environment.
Job Type & Location
This is a Contract to Hire position based out of Columbus, OH.
Pay And Benefits
The pay range for this position is $26.00 - $27.50/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 & 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 Mar 2, 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 actalentaccommodation@actalentservices.com for other accommodation options.
Salary : $26 - $28