QA Specialist
Swisslinx
Visp
Key information
- Publication date:09 January 2026
- Workload:100%
- Contract type:Temporary
- Language:English (Fluent)
- Place of work:Visp
- Act as QA representative in Project teams and represent QA in meetings
- Act as QA contact for specific topics and realize the…
Job description:
- Act as QA representative in Project teams and represent QA in meetings
- Act as QA contact for specific topics and realize the interface for DRs and CRs
- Act as point of contact for Drug Product QA related questions, topics and complaints from customers related to the manufacturing operations
- Support and approve risk assessments or regulatory specific risk or gap assessments.
- Review and release product specific documentation such as process descriptions and workflows, recipes, manufacturing protocols, transfer documents, test plans, parameter lists, etc.
- Represent Drug Product QA topics during regulatory inspections.
- Support continuous improvement programs to establish an effective Quality Management System for Visp DPS.
- Represent Quality Assurance in cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project- and Site
- Engineering project / technology transfer to effectively execute tasks related to Drug Product processes.
- Assess, review and approve quality records and release files/dossiers e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs, in line with current local SOPs.
Requirements:
- University degree or equivalent in Chemistry / Biology / Biotechnology or a related field
- Long-term experience working in the GMP environment of the pharmaceutical industry
- Experience working in a QA department Drug Product
- English language skills are required, German language is an advantage
