- 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 surrounding GMP activities.
- Work closely with GMP management to ensure continuous improvement objectives are identified and met using metrics and other statistical means.
- Operate and perform the 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 culture, biology, cell culture, microbiology, mammalian and eukaryotic systems.
- 1-2 years of experience in the scientific industry is preferred.
- Comfortable with occasionally lifting/pushing/pulling 30-45lbs.
- Associate degree in Science is preferred.
- Experience in Aseptic Processing or GMP is required.
- Experience in Drug Compounding, Drug Manufacturing, Food Manufacturing/FDA is advantageous.
- Long-term interest and desire to be in the Science Field.
The work environment is team-oriented and diverse, with strong growth opportunities as the team moves into a new state-of-the-art facility. Most of the day will be spent on feet, with gowning up required for clean room access. The dress code is casual lab attire, including closed-toed shoes, socks covering ankles, khaki pants or jeans without holes, and shirts without large graphics. The shift is Monday to Friday, from 7:00 AM to 5:30 PM, with flexibility for scheduling adjustments as needed.
Pay and Benefits The pay range for this position is $22.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your jobclassification 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 Aug 8, 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.