QA Specialist – Quality Systems / Document Management (m/f/d)
This job offer is no longer available.
Switzerland | 
Temporary Employment
General Conditions
- Workload: approx. 50% (4 hours per day—remote work possible)
- Project duration: initially approx. 6 months
- Start: ASAP
Responsibilities
- Conducting formal and substantive compliance checks
- Review of SOPs, VOIs, work instructions, and technical and quality-related documents
- Reducing and systematically processing the existing document backlog (Mastercontrol)
- Verifying file names, document types, authors, departments, and document assignments
- Ensuring correct department and approval assignments
Required Qualifications
- Experience in the pharmaceutical, chemical, or biotechnology quality field
- Experience in quality systems and document management (Mastercontrol)
- Very good understanding of GMP and compliance
Reference number: 17691
Industry: Pharmaceutical Industry
Project start: ASAP
Duration: 6 months
Employment type: Temporary Employment
Contact
Eva Joy Schmidt
