On-Site QMS & Document Control Specialist (IVD)

Proclinical Group is seeking a Document Control Specialist for a 12-month contract in London. The role involves managing the Quality Management System documentation, ensuring compliance with ISO 13485 and FDA 21 CFR Part 820.

The ideal candidate will have prior experience in document control, strong organizational skills, and the ability to work independently. The position offers a competitive salary and benefits within a rapidly growing healthcare organization.

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