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Specialist I, QA Batch Release
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- The QA Specialist I, Batch Release is responsible for performing duties related to the management of records relevant to the review and release of Batch Records for the CGMP operation of Emergent BioSolutions in Baltimore Camden Site. Our QA Department provides expertise in problem solving and process improvements.
- The QA Specialist I will interact with all departments to provide guidance necessary to maintain and improve CGMP compliance at the company.
- Coordinate batch record review and approval process.
- Compile and communicate performance metrics and data trend analyses to senior management for Batch Review and Release relevant activities.
- BS or BA degree in Science or Engineering with 5-10 years of GMP experience with at least one year in an FDA regulated industry.
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