Quality Compliance Specialist (m/f/d)
Über uns
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.Aufgaben
- Lead and continuously improve the GMP self-inspection program, including annual planning and execution
- Coach SMEs and audit teams to ensure strong inspection and self-inspection readiness
- Perform gap assessments on global procedures and drive alignment across site functions
- Coordinate cross-functional activities and ensure effective communication with all departments
- Support internal, external, and mock audit preparation, including document review and QA input
- Act as backroom/ACC or scribe team member during audits and inspections
- Serve as Data Integrity Champion and ensure consistent DI implementation across the site
- Prepare and present compliance topics to the Quality Council and site leadership
- Support continuous improvement initiatives and coordinate operational activities within the compliance team
- Act as back-up for the Quality Compliance & Systems Expert when required
Profil
- University degree in biochemistry, chemistry, engineering, or another relevant scientific/technical discipline
- Solid experience in biotechnology and/or pharmaceutical industry
- Strong knowledge of GMP requirements and Quality Systems
- Understanding of manufacturing, QC laboratory, and warehouse processes for biological products
- Solid knowledge of Good Documentation Practices (GDDP) and Data Integrity principles
- Experience supporting audits and regulatory inspections
- Skilled in writing, reviewing, and updating SOPs and technical documentation
- Familiarity with risk management tools (FMEA, RCA, etc.)
- Proficiency in French and English (minimum B2)
- Experience with eQMS tools (e.g., Veeva Vault, TrackWise), Microsoft Office, SharePoint, and Power BI
Wir bieten
- A very renowned company
- Continuous support during the assignment
- Individual all-round care: Support throughout the entire application phase
Ihr Kontakt
Referenznummer
864224/1
Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch
Anstellungsart
Freiberuflich für ein Projekt