Job information

Posted:

Job reference: a7adb9956bb0f bbed1a560fd5

Client / Employer: Proclinical

Location: TN Switzerland · Canton of Lucerne, Switzerland

Closing date:

Role overview

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