- Minimum A.S. degree in biology, chemistry, or related technical field, or equivalent industry experience.
- 1+ years of experience in biopharmaceutical-based GMP manufacturing operations
- 1+ years of experience performing mammalian cell culture
- A background in cell culture, aseptic gowning and qualification, and/or ISO class 7 cleanroom operations is required.
- Demonstrated technical knowledge of aseptic processing in cleanroom environmentsThe Cell Manufacturing Associate will:
- Follow compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs) and understands 'why' behind the regulations. Able to coach and mentor others to do the same
- Identify communicate, address and improve complex cGMP compliance and regulatory gaps and issues
- Follow, execute, author, and improve the efficiency and execution of Standard Operating Procedures (SOPs) and Batch Records (BRs)
- Train others on SOPs, equipment, all unit operations and non-manufacturing SOPs and systems
- Responsible for the manufacturing of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs).Compensation:
$27 hourly
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at (+1) or
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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Cell Manufacturing Associate - Philadelphia, United States - Proclinical Staffing
Description
Cell Manufacturing Associate - Contract - Onsite
Proclinical Staffing is seeking an Aseptic Processing Technician to join a cutting-edge biotech company. This is a contract role located in Philadelphia, PA.
Skills & Requirements:
