GMP Documentation Specialist - Pharma Production
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Manufacturing / Production
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Pharmaceutical
Job Description & How to Apply Below
Siegfried in Irvine, CA seeks a Production Documentation Associate to ensure GMP-compliant manufacturing documentation and batch records. You will investigate deviations and contribute to CAPAs, working with multiple departments to maintain accurate records and regulatory readiness.
The role requires a scientific degree and substantial pharmaceutical experience, with strong problem-solving, writing, and collaboration skills.
The GMP Documentation Specialist
- Pharma Production role at Quick Cruit, Inc. is now open for applications in Irvine, CA, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Documentation Specialist
- Pharma Production role in the description above.
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