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.

Also on the board Same function, level within a rung

Level

Senior

Location

Gainesville, FL

Occupation

Regulatory Affairs Specialists

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

Apply for this role →