ProPharma Group is seeking a QA Lead to support Person-In-Plant activities across UK/EU CDMO partners. The role is 1.0 FTE with travel to sites for several weeks and offers hybrid working. It requires quality leadership across GMP/QA activities and inspection readiness support.
Responsibilities include QMRs, PPQ support, audits, CAPAs, and cross-functional collaboration. Fluent English and a life-sciences background are essential for success.
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Senior Quality Lead, Life Sciences (CDMO/PIP) employer: ProPharma Group
ProPharma Group is an exceptional employer located in Greater London, offering a part-time Senior Clinical Research Associate role that promotes a healthy work-life balance. With a strong commitment to diversity, equity, and inclusion, the company cultivates a supportive work culture where employees are encouraged to grow professionally through continuous learning opportunities. Joining ProPharma means being part of a dynamic team dedicated to advancing clinical research while enjoying the unique advantages of working in one of the UK's most vibrant cities.
