Contract till end of year - OSD Manufacturing
Location: French-speaking Switzerland (Romandie)
Duration: 6 months (temporary contract)
Languages: French required, English fluent
A leading pharmaceutical site in French-speaking Switzerland is seeking an experienced Senior Validation Scientist or Engineer to support a major equipment qualification project in an oral solid dosage (OSD) manufacturing environment. This is a temporary assignment within the MS&T team, focusing on revamping a tableting production area in a GMP-regulated setting.
Your Responsibilities:
- Lead the commissioning and qualification of production equipment and computerized systems (CSV)
- Define and implement qualification strategies (DQ, FAT, SAT, IQ, OQ, PQ)
- Collaborate closely with cross-functional teams (Engineering, QA, MS&T, Production, Suppliers)
- Review and author qualification protocols and reports in alignment with industry and regulatory standards
- Ensure execution of qualification activities in accordance with internal standards and budget
- Support audits and inspections as SME for validation documentation
- Initiate and manage change controls, investigations, and CAPAs related to qualification
Your Profile:
- Degree in Engineering or Life Sciences
- Minimum 5 years of experience in validation or qualification within the pharmaceutical industry (GMP environment, OSD experience preferred)
- Solid knowledge of equipment and CSV validation practices
- Hands-on experience in project and change management
- Proactive communicator with strong documentation skills
- Comfortable navigating a cross-functional and dynamic project setting
- Fluency in French is required, good command of English essential
Are you ready to make an impact in a project that contributes to safe and efficient pharmaceutical manufacturing? We look forward to hearing from you.