GMP Manufacturing Associate
Day Shift
Kelly Science is looking for a GMP Manufacturing Associate to join a leading biopharmaceutical company in Oklahoma City, OK.
Job Responsibilities :
- Execute and monitor GMP manufacturing processes for cell culture-based production, ensuring compliance with protocols and regulations.
- Perform routine tasks like media prep, cell inoculation, bioreactor operation, and harvest operations with precision and attention to detail.
- Collaborate with cross-functional teams (Quality Control, Quality Assurance) to ensure product quality and regulatory compliance.
- Troubleshoot and resolve process issues, identifying root causes and implementing corrective actions to maintain efficiency.
- Document all manufacturing activities according to GMP standards, maintaining accurate and complete batch records.
- Participate in technology transfer activities, sharing your cell culture expertise and contributing to process improvement initiatives.
- Maintain a clean and organized work area, following safety protocols. Qualifications :
- High School Diploma / equivalent OR Bachelor's degree in a relevant scientific field (Biotechnology, Biochemistry, Biology, etc.) is a plus
- 1-3 years of hands-on experience in GMP manufacturing, focused on cell culture processes.
- Strong knowledge of bioreactor operations, aseptic techniques, and upstream processing.
- Familiarity with biopharmaceutical production regulations (FDA, EMA).
- Excellent problem-solving and analytical skills for troubleshooting and process optimization.
- Effective communication and teamwork skills to collaborate across departments and foster a positive team environment.
- Detail-oriented with the ability to maintain accurate documentation according to GMP standards.
Job Details :
- Temp-to-Hire
- $22 hourly pay rate
- Day Shift
9370695
GMP Manufacturing Associate
Kelly Science is looking for a GMP Manufacturing Associate to join a leading biopharmaceutical company in Oklahoma City, OK. Execute and monitor GMP manufacturing processes for cell culture-based production, ensuring compliance with protocols and regulations. Document all manufacturing activities ac...
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