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Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our…
Oversee physical and procedural security at a biopharma site: patrol facilities, monitor alarms, investigate incidents, manage access systems, and mentor a team of security officers on third shift.
Performs visual inspection and quality checks on biopharma products during manufacturing to ensure GMP compliance and patient safety.
Coordinates biopharma packaging projects, manages orders and documentation in ERP systems, and ensures regulatory compliance for life-saving therapies.
Review batch records, approve investigations, and ensure GxP compliance for biopharma manufacturing, shaping quality systems for clinical and commercial products.
Perform real-time GMP quality assurance for biopharma manufacturing, including floor oversight, batch record review, AQL inspections, and issue resolution to ensure regulatory compliance and patient safety.
Design, optimize, and maintain pharmaceutical fill-finish equipment; troubleshoot issues and lead validation to ensure compliant, efficient production.
Oversee custom drug-product projects for biopharma clients, coordinating timelines, budgets, and cross-functional teams to deliver therapies on time and within scope.
Validation Analyst I writes and executes compliance protocols for biopharma systems, ensuring adherence to cGMP and FDA rules while supporting audits and change control.
Coordinates review and approval of GMP documents using an electronic system, manages archival, and interfaces with authors to meet timelines in a biopharma services role.
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