Job Description
Document Control Specialist - In Vitro Diagnostics
Location: London (fully site-based)
Duration: 12 Month Contract
Pay: Competitive Rate
Proclinical is partnered with a regulated healthcare organisation operating within medical and in-vitro diagnostics. Due to continued expansion they are looking to hire a Document Control Specialist to join their Quality team at their London offices.
This role will be responsible for the day?to?day management of Quality Management System (QMS) documentation, ensuring all controlled documents are compliant with ISO 13485 and FDA 21 CFR Part 820 requirements.
Key Responsibilities of the Document Control Specialist
Manage and maintain controlled QMS documentation in line with internal procedures
Coordinate document creation, review, approval and distribution workflows
Monitor document revisions and manage document change orders
Maintain an accurate and up?to?date electronic document management system
Su...
Location: London (fully site-based)
Duration: 12 Month Contract
Pay: Competitive Rate
Proclinical is partnered with a regulated healthcare organisation operating within medical and in-vitro diagnostics. Due to continued expansion they are looking to hire a Document Control Specialist to join their Quality team at their London offices.
This role will be responsible for the day?to?day management of Quality Management System (QMS) documentation, ensuring all controlled documents are compliant with ISO 13485 and FDA 21 CFR Part 820 requirements.
Key Responsibilities of the Document Control Specialist
Manage and maintain controlled QMS documentation in line with internal procedures
Coordinate document creation, review, approval and distribution workflows
Monitor document revisions and manage document change orders
Maintain an accurate and up?to?date electronic document management system
Su...