QA Lead, Life Sciences & CDMO Partnerships

ProPharma is seeking a Quality Assurance Lead to support Person-In-Plant activities across CDMO partners in the EU. The role is a short-term engagement starting immediately with 1.0 FTE (40 hours/week) and travel to UK/EU sites for two to three weeks at a time.

You will lead QMRs, oversee PPQ activities, coordinate audits, and drive inspection readiness while ensuring GMP compliance and alignment with ProPharma standards.

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