MedPharm is seeking a QA Specialist to provide QA support for IMP manufacturing and related QMS. You will review quality documentation, manage QMS records, and oversee QA activities across manufacturing and laboratory operations to ensure compliance with GMP, GCP, GLP and regulatory requirements.
The role requires experience in deviations, CAPAs, change controls, and audits, with strong data integrity and GDP knowledge.
#J-18808-LjbffrQA Specialist: GMP & Compliance for IMP Manufacturing 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.
