Technical Document Manager
Key information
- Publication date:29 August 2025
- Workload:100%
- Contract type:Temporary
- Language:English (Fluent)
- Place of work:Visp
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:
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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.
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Document Control & Lifecycle Management
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Own the end-to-end lifecycle of technical project documents including, but not limited to:
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URS (User Requirement Specifications)
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TS (Technical Specifications)
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FDS (Functional Design Specifications)o P&IDs (Piping and Instrumentation Diagrams)
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Drawings, datasheets, design reviews, and vendor documentation
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Ensure compliance with internal documentation standards, GMP requirements, and quality records expectations
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Facilitate document creation, updates, and controlled revisions with relevant stakeholders(engineering, QA, production, validation, EPCM)
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Workflow Coordination: Initiate and manage review and approval workflows in document management systems (e.g.Documentum (DMS) or equivalent)
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Interface Management: Act as a liaison between internal departments (production, engineering, QA, validation) and external EPCM partners for technical documentation exchange
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GMP Change Documentation: Support the preparation, linkage, and maintenance of change control documentation (TCRs/CRs)
Qualifications:
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Degree in Engineering, Life Sciences (preferably biopharmaceuticals), Technical Writing, or related field
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3+ years of experience in a regulated GMP environment, preferably in pharma/biotech
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Proven experience in document management or technical documentation within CapEx or OpEx projects
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Familiarity with GMP-compliant change management processes (CRs/TCRs)
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Strong knowledge of technical documentation and engineering terminology (URS, P&ID, FDS, etc.)
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Experience with electronic document management systems (EDMS) with a detail-oriented and methodical approach
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Fluency in English (written and spoken); German is an asset
About the company
Reviews
- Management style4.5
- Salary and benefits3.5
- Career opportunities4.0
- Working atmosphere4.5