CAPEX Document Controller | CAPEX Document Controller (m/w/d)

Tech'Firm Industrie AG

Stein AG, AG, Switzerland
Published Dec 5, 2025
Full-time
Permanent

Job Summary

This critical role involves serving as a CAPEX Document Controller for a major pharmaceutical client, ensuring all project documentation adheres strictly to regulatory standards, particularly GMP and GLP. The specialist will be responsible for establishing, maintaining, and auditing an efficient document control system, including accurate storage, retrieval, versioning, and access control within electronic repositories. Success requires meticulous attention to detail and strong organizational skills to manage documentation across cross-functional teams. This position offers the opportunity to contribute document control expertise to an industry-leading pharma company, directly impacting the integrity of life-saving medication documentation in a highly regulated, fast-paced environment. Candidates must possess professional experience in document control within the pharmaceutical sector and be fluent in both German and English.

Required Skills

Education

Bachelor’s degree or equivalent in pharmacy, life sciences, or related fields

Experience

  • Proven experience in document control within the pharmaceutical environment
  • Strong knowledge of GMP and GLP requirements
  • Professional experience collaborating across cross-functional teams
  • Experience conducting regular internal audits of documents

Languages

German (Fluent)English (Fluent)

Additional

  • Ability to manage multiple priorities efficiently in a fast-paced, regulated environment; High integrity and discretion when handling confidential information.