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(URGENTLY HIRING) Job Title: GMP Documentation Technician 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. Responsibilities + Manage the creation, revision, storage, and retrieval of all controlled documentation. + Ensure compliance with GMP regulations and internal quality systems. + Perform essential Document Control functions in a timely manner to support efficient manufacturing operations. + Register controlled documents and monitor and communicate revision and review cycles. + Issue production documents and assist with organizing and maintaining the QA Documents Room. + Scan, file, and archive GMP records according to internal procedures and regulatory requirements. Essential Skills + 3+ years of industry experience + Prior experience with document control + Experience working with GMP or FDA regulations + Understanding of regulatory and documentation constraints in a GMP environment + Excellent communication and writing skills + Proficiency in Word and Excel Additional Skills & Qualifications + BS Degree in Sciences preferred Work Environment This is a quickly growing new company in the startup phase, currently building two new sites in Columbus, Ohio. The facility features state-of-the-art clean rooms and equipment. Employees work in cross-functional teams, contributing to a dynamic and innovative 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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 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 7, 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 ( ) for other accommodation options.