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Job Title: GMP Scientist I / GMP Operations Technician I

Job Description

The GMP Scientist I / GMP Operations Technician I supports all aspects of Good Manufacturing Practices (GMP) and production within a Clinical Manufacturing facility. In close collaboration with GMP Operations leadership and production staff, this role provides hands-on support for day-to-day GMP and Viral Vector Core manufacturing activities, including execution of production processes, documentation, and facility and equipment maintenance. The position focuses on cell-based manufacturing in a GMP environment, ensuring that all biological products are produced in a timely, compliant, and cost-effective manner by following batch records and Standard Operating Procedures (SOPs). This is not a research-based role and is ideal for individuals who want to build a long-term career in the scientific and manufacturing field.

Responsibilities

• Support all aspects of GMP operations and production in the Clinical Manufacturing facility, with a focus on cell-based manufacturing.
• Execute GMP and Viral Vector Core production processes according to approved batch records and Standard Operating Procedures (SOPs).
• Assist with day-to-day manufacturing activities to ensure timely, compliant, and fiscally responsible delivery of biological products.
• Support GMP resources and the supply chain by ordering materials and maintaining inventory to meet production goals.
• Ensure the availability of materials with proper documentation and traceability in alignment with GMP requirements.
• Work closely with GMP management to identify continuous improvement opportunities and help achieve objectives using metrics and other statistical tools.
• Operate facility equipment and systems as specified in SOPs, including performing calibration, validation, and routine cleaning.
• Assist in the review, revision, and remediation of process documentation, including batch records and SOPs.
• Support process change controls by documenting changes accurately and maintaining compliance with GMP standards.
• Spend approximately 50–75% of time working in the laboratory and clean room performing hands-on production activities.
• Spend approximately 25% of time supporting documentation, paperwork, and preparation for upcoming process steps.
• Follow aseptic techniques and clean room procedures to maintain a controlled and compliant manufacturing environment.
• Handle and move materials and equipment safely, including occasionally lifting, pushing, or pulling 30–45 pounds.
• Collaborate effectively with a diverse, team-oriented group to support a growing, start-up-phase operation within a state-of-the-art facility.

Essential Skills

• Experience working in an aseptic processing or GMP manufacturing environment.
• Background in drug compounding, drug manufacturing, or food manufacturing regulated by the FDA.
• 2–3 years of experience in the scientific industry preferred.
• Knowledge and understanding of aseptic technique and clean room practices.
• Experience or familiarity with cell culture, including mammalian or eukaryotic cell-based processes.
• Understanding of liquid separation techniques relevant to biological manufacturing.
• Foundational knowledge in biology, microbiology, tissue culture, and cell biology.
• Ability to operate laboratory and production equipment in accordance with SOPs.
• Comfort with occasionally lifting, pushing, or pulling 30–45 pounds as part of routine duties.
• Strong attention to detail and commitment to following GMP documentation and procedures.
• Long-term interest and desire to build a career in the science and manufacturing field.
• Effective teamwork and communication skills in a collaborative production environment.

Additional Skills & Qualifications

• Associate’s degree in a scientific discipline preferred.
• Prior hands-on experience with mammalian or eukaryotic cell culture is a strong plus.
• Experience working in tissue culture or cell-based laboratory environments.
• Exposure to laboratory operations involving microbiology, tissue biology, or related fields.
• Ability to support continuous improvement initiatives using metrics and basic statistical methods.
• Comfort working in a fast-growing, start-up-phase environment within a larger supported organization.
• Willingness to work primarily in a non-research, production-focused role.

Work Environment

The work environment is a highly collaborative, team-oriented Clinical Manufacturing facility with a diverse group of professionals who are continuing to grow and expand operations. The organization is moving into a new, state-of-the-art facility and operates in a start-up phase with strong institutional backing. Approximately 50–75% of the role involves working in laboratories and clean rooms, performing hands-on cell-based manufacturing in a GMP environment. The remaining time is dedicated to documentation, paperwork, and preparation for subsequent process steps. Team members spend most of the day on their feet and regularly gown up to enter clean rooms, following strict aseptic and GMP protocols. The standard shift is Monday through Friday, 8:00 a.m. to 5:00 p.m. Dress code consists of casual lab attire, including closed-toe shoes, socks covering the ankles, khaki pants or jeans without holes, and shirts without large graphics, with additional gowning requirements when entering clean rooms.

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

The pay range for this position is $24.00 - $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)

This is a fully onsite position in Columbus,OH.

This position is anticipated to close on Aug 17, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.