About the role

Boehringer Ingelheim is seeking a QA Release professional to review batch records, ensure regulatory compliance, and support release documentation for biologics. You will act as a deputy to the Qualified Person and collaborate with QA, manufacturing, and regulatory teams. Responsibilities include review of COAs, change controls, deviations, CAPAs, and SAP movements. The role requires hands-on expertise in regulatory requirements and excellent documentation skills.

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JOB OVERVIEW

Experience level

Senior

Location

Gainesville, FL

Occupation

Regulatory Affairs Specialists

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

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