Technical Document Manager

Posted on August 27, 2025
Visp
English
Temporary
Posted on August 27, 2025

About this role

For our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases. 




 

Key Responsibilities:

 

  • Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpEx improvements executed by internal production teams, all within a regulated GMP framework.

  • Document Control & Lifecycle Management

  • Own the end-to-end lifecycle of technical project documents including, but not limited to:

  • URS (User Requirement Specifications)

  • TS (Technical Specifications)

  • FDS (Functional Design Specifications)o P&IDs (Piping and Instrumentation Diagrams)

  • Drawings, datasheets, design reviews, and vendor documentation

  • Ensure compliance with internal documentation standards, GMP requirements, and quality records expectations

  • Facilitate document creation, updates, and controlled revisions with relevant stakeholders(engineering, QA, production, validation, EPCM)

  • Workflow Coordination: Initiate and manage review and approval workflows in document management systems (e.g.Documentum (DMS) or equivalent)

  • Interface Management: Act as a liaison between internal departments (production, engineering, QA, validation) and external EPCM partners for technical documentation exchange

  • GMP Change Documentation: Support the preparation, linkage, and maintenance of change control documentation (TCRs/CRs) 




 

Qualifications:

 

  • Degree in Engineering, Life Sciences (preferably biopharmaceuticals), Technical Writing, or related field

  • 3+ years of experience in a regulated GMP environment, preferably in pharma/biotech

  • Proven experience in document management or technical documentation within CapEx or OpEx projects

  • Familiarity with GMP-compliant change management processes (CRs/TCRs)

  • Strong knowledge of technical documentation and engineering terminology (URS, P&ID, FDS, etc.)

  • Experience with electronic document management systems (EDMS) with a detail-oriented and methodical approach

  • Fluency in English (written and spoken); German is an asset

 

 

 

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