Join a major pharma organisation to support GMP‑compliant document management across engineering and operations for a 6 month project with a January start date.
Responsibilities
* Maintain document control systems and ensure accurate versioning
* Manage storage, retrieval, and distribution of controlled documents
* Support document creation, review, and approval workflows
* Perform internal audits and address compliance issues
* Train users on document control procedures
* Prepare documentation for regulatory inspections
Requirements
* Experience in pharma/GMP document control
* Strong understanding of GMP/GLP standards
* Excellent organisation and attention to detail
* Fluent German and English
* Proficient with document management tools and MS Office
Seniority Level
Mid‑Senior level
Employment Type
Contract
Job Function
Administrative
Industry: Pharmaceutical Manufacturing
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