Bimeda in the United Kingdom (Wales) is seeking a QA/QMS Documentation Specialist to maintain site QA/QMS systems and oversee documentation control for finished products and packaging materials.
The role involves reviewing release documentation, assisting in SOPs, and drafting CoA/CoC in line with GMP/GDP requirements. A detail-oriented, self-driven candidate with strong MS Office skills is preferred.
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QA Documentation & Compliance Specialist employer: Bimeda
Bimeda is an exceptional employer located in Cambridge, ON, offering a dynamic work environment where innovation meets compliance in the pharmaceutical manufacturing sector. With a strong focus on employee growth, competitive benefits including generous vacation policies and comprehensive health coverage, Bimeda fosters a culture of continuous improvement and collaboration, ensuring that every team member can thrive while contributing to the health and wellbeing of animals globally.
