QA Expert Analytics 9 months fix-term contract 80-100% (f/m/d)
CHF 93K-174K (estimate) Senior-level Contract Full Time
Tasks
- Author review and approve GMP documents
- Ensure GMP quality manual compliance
- Ensure compliance with GMP and quality standards
- Perform review and approval in DMS
- Perform review and approval in LIMS
- Provide QA support to QC functions for GMP analytical testing
- Review and approve CAPA
- Review and approve OOS investigations
- Review and approve analytical method validation
- Review and approve change controls
- Review and approve deviations
- Review and approve release testing
- Review and approve specifications
- Review and approve stability studies
- Support analytical release activities
- Support customer audits
- Support health authority inspections
- Support technical release of drug product batches
Perks/Benefits
- N/A
Skills/Tech-stack
Analytical method validation | CAPA | Change Control | DMS | Deviation Management | Document Management | Document Management System | GMP | HSE | Information Management System | LIMS | Laboratory Information Management | Laboratory Information Management System | Laboratory information | Management System | Method validation | OOS Investigation | Quality Assurance | Quality Control | Stability Studies | TrackWise
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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