- Pay: $28-34.53/hr.
- Must be flexible to work the following schedules:
- Sun–Wed or Wed–Sat, with shifts from 6:00am–4:30pm or 3:00pm–1:30am.
- 4-month assignment with possibility for extension or conversion based on performance and budget.
- Perform and verify manufacturing tasks in accordance with batch records, SOPs, and cGMP requirements to support commercial cell therapy production.
- Operate, monitor, clean, and prepare automated cell processing, cell expansion, and filling equipment within Grade B/C cleanrooms while following all gowning and PPE protocols.
- Identify, troubleshoot, and escalate process or equipment issues to ensure safe, compliant, and efficient manufacturing operations.
- Complete all required technical and cGMP training assignments to maintain operational readiness and compliance.
- Author and revise SOPs and documentation to ensure clarity, technical accuracy, and alignment with regulatory and operational standards.
- Support continuous improvement by identifying process efficiencies and assisting with investigations, deviations, and change controls.
- Collaborate closely with Materials Management, Quality Control, and Quality Assurance to execute GMP manufacturing runs.
- Safely handle cleaning agents and wear a respirator during designated cleaning procedures as required.
Degree Requirements:
- Bachelor’s Degree in Life Sciences Field
- Associates Degree in Life Sciences Field with 1+ years of biotech experience or
- High School Diploma with 2+ years of cGMP experience
- cGMP experience required
- Experience with cell therapy/cell culture required, mammalian cells preferred
- Experience with troubleshooting any processes or equipment preferred
- Experience with automated cell processing/cell expansion and filling equipment is preferred
- Experience with assisting with investigations, deviations, and/or change controls preferred
If you are interested in hearing more about the position, please respond to this posting with your resume attached.
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