Document Control Specialist

Be the backbone of GMP excellence—ensuring precision, compliance, and control across critical manufacturing documentation.

Proclinical is seeking a Document Control Specialist to support documentation processes for a project in the cardiovascular manufacturing sector. In this role, you will ensure the efficient management, organization, and execution of document-related tasks while adhering to GMP standards. This position requires attention to detail, organizational skills, and the ability to work within established timelines to meet business and project objectives.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities

• Manage the execution and tracking of documents, including obtaining necessary signatures and verifying approvals.
• Ensure proper handling, organization, and archiving of company documentation in compliance with internal standards.

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