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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QA Lead, Life Sciences & CDMO Partnerships employer: ProPharma
ProPharma is an exceptional employer that fosters a culture of diversity, equity, and inclusion, empowering employees to be their authentic selves while driving innovation in the healthcare sector. With a commitment to employee growth, ProPharma offers opportunities for professional development and collaboration, particularly in its Eastern European hubs, where remote work is supported alongside hybrid office engagement. Join us to make a meaningful impact in the field of compliance and quality assurance, all while enjoying a supportive and dynamic work environment.
