Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø

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

Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø 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.
• Verify and update Certificates of Analysis (CoA) and TSE-BSE documentation for raw material release under GMP guidelines.
• Input, index, and archive documents and data into the company's document management system.
• Perform quality checks on documents, ensuring metadata accuracy and compliance with regulatory requirements.
• Collaborate with cross-functional teams to meet project deadlines and changing business needs.

Key Skills and Requirements:

• Experience in document control or a similar role, preferably within a GMP-regulated environment.
• Familiarity with managing CoA and TSE-BSE documentation.
• Proficiency in English (mandatory); German at a B1 level is required.
• Strong organizational skills and attention to detail.
• Ability to work effectively within tight deadlines and adapt to evolving project requirements.
  

If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at o.worch@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy