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The Quality Engineer designs and maintains the Quality Management System for pharmaceutical manufacturing, ensuring compliance with GMP standards. They manage deviations, CAPA, validation protocols, and internal/external audits to support product quality and regulatory readiness.
QA Specialist ensures pharmaceutical manufacturing and lab processes meet GMP, GCP, and GLP standards by reviewing documentation, managing quality systems, and supporting compliance audits in Guildford, UK.
Position Summary – The Cleaning Validation Engineer oversees the development, maintenance, and governance of MedPharm’s site-wide cleaning validation program across the full product lifecycle, from development through…
Job Purpose: The Manager of EHS is responsible for leading the Environmental Health and Safety programs and activities in support of MedPharm US sites, including the GMP pharmaceutical manufacturing site and the…
Project Manager Onsite | Durham, NC | Full-Time Position Summary – The Project Manager plays a critical role in leading and executing client programs across MedPharm’s end-to-end CDMO services. This client-facing…
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