Biotech Operations Support Technician

The GMP Operations Technician is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing Facility. Collaborating with the Manager of GMP Operations and staff, the Technician will provide hands-on assistance for all day-to-day GMP and Viral Vector Core production operations, including the execution of production processes, documentation, as well as facility and equipment maintenance. This role supports production efforts to deliver all products in a timely, compliant, and fiscally responsible manner by following appropriate practices, batch records, and Standard Operating Procedures (SOPs) for manufacturing biological products.

Responsibilities

• Support GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals.
• Support daily operational activities related to the GMP manufacturing of biological products by ensuring the availability of materials with proper documentation.
• Collaborate closely with GMP management to identify and meet continuous improvement objectives using metrics and statistical means.
• Operate and perform calibration, validation, and cleaning of all facility equipment and systems as specified in SOPs.
• Assist in process documentation review, revision, remediation, and process change controls.

• Experience in GMP, tissue biology, cell culture, microbiology, and mammalian eukaryotic laboratory environments.
• Prefer an Associate degree in Science.
• Experience in aseptic processing or GMP environments.
• Experience in drug compounding, drug manufacturing, food manufacturing/FDA regulations.
• 1-2 years of experience in the scientific industry preferred.

• Long-term interest and desire to be in the Science Field.
• Comfortable occasionally lifting, pushing, or pulling 30-45 lbs.

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 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 Jul 29, 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 ... for other accommodation options.