MedPharm is seeking a QA Specialist to provide Quality Assurance support for IMP manufacturing and related QA systems. The role collaborates with Production, QC, and Development to ensure GMP/GCP/GLP compliance, review quality documentation, and maintain data integrity across quality records and investigations.
Responsibilities include QMS management, document control, batch release support, supplier qualification, and audits.
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QA Specialist: GMP/GCP/GLP Compliance Expert in England employer: MedPharm
As a Process Technician in our cGMP-compliant biopharmaceutical manufacturing environment, you will be part of a dynamic team that values safety, quality, and continuous improvement. We offer a supportive work culture that encourages professional growth through training and development opportunities, ensuring you can thrive in your role while contributing to meaningful advancements in healthcare. Located in a state-of-the-art facility, we provide a collaborative atmosphere where your skills and expertise will be recognised and rewarded.
