Technical Document Manager m/f/d, Wallis The Technical Document Manager is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases - from detailed design through execution and performance qualification (PQ).
The scope includes both Cap Ex-driven mechanical adaptations managed by external engineering (EPCM) partner and Op Ex improvements executed by internal production teams, all within a regulated GMP framework.
Contract duration: until 31.08.2026 Responsibilities Document Control & Lifecycle Management Own the end-to-end lifecycle of technical project documents 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) Initiate and manage review and approval workflows in document management systems (e.g.
Documentum (DMS) or equivalent) Track and follow up on sign-offs and ensure timely completion of review cycles Ensure document traceability and audit readiness across all phases of the project Act as a liaison between internal departments (production, engineering, QA, validation) and external EPCM partners for technical documentation exchange Coordinate handover and archiving of EPCM-generated documents into internal systems Support alignment between Cap Ex documentation and Op Ex procedural updates or GMP-relevantchanges Support the preparation, linkage, and maintenance of change control documentation (TCRs/CRs) with associated technical documents Ensure traceability of changes from requirements through qualification Experience 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 Cap Ex or Op Ex 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) Jetzt bewerben Sounds like a great job?Then we look forward to receiving your complete application documents through our online application form.
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