On-Site In-Process QA Specialist (GMP)

NIVAGEN PHARMACEUTICALS

Sacramento, CA

JOB DETAILS
SKILLS
Biology, Biotech and Pharmaceutical, Continuous Improvement, Documentation, GMP (Good Manufacturing Practices), Manufacturing/Industrial Processes, Quality Assurance, Quality Metrics, Testing, Time Tracking
LOCATION
Sacramento, CA
POSTED
Today

A global pharmaceutical company located in Sacramento is seeking an In Process QA Specialist to ensure quality standards during manufacturing processes. Key responsibilities include real-time monitoring, testing, and documentation in line with Good Manufacturing Practices. The ideal candidate will have a Bachelor's degree in Life Sciences or related field and up to three years of relevant experience. The position fosters a culture of quality and continuous improvement, offering competitive pay and comprehensive benefits.#J-18808-Ljbffr

About the Company

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NIVAGEN PHARMACEUTICALS