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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