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16443en
- Contract
- English
- Associate
- Research & Development
- Switzerland
- Healthcare & Life Sciences
Skills
Pharma, Biotech, QA, QA Qualification, FAT, SAT, IQ, OQ, PQ processes, SAP
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This vacancy has now expired
On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a Quality Engineering Specialist to support qualification activities for technical facilities, equipment, and systems. This is an exciting opportunity to play a key role in ensuring compliance and quality within a dynamic and collaborative environment.
Contract Type: Contract
Start Date: ASAP
Location: Visp, Switzerland
Workload: 100%
Duration: 4 months
Your Mission
• Oversee quality-related responsibilities for daily qualification activities on technical facilities, equipment, and systems.
• Support the development, review, and release of qualification documents.
• Approve qualification documents and assess change requests for relevance to the qualified state, including supporting and approving quality risk analyses (e.g., GMP-FMEA).
• Ensure deviations are investigated and addressed appropriately in deviation reports.
• Maintain compliance with legislation, authority guidelines, and customer expectations.
• Report relevant developments and trends to the QA Qualification Group Manager.
• Contribute to the formulation and development of qualification strategies and participate in continuous training.
• Support internal audits, customer audits, and official inspections as a QA representative.
Your Background
• Proven experience in the biotechnology or pharmaceutical industry.
• Expertise in QA Qualification, including knowledge of FAT/SAT/IQ/OQ/PQ processes.
• Proactive, with strong communication skills and the ability to work effectively in a multidisciplinary team.
• Fluency in English (spoken and written).
Beneficial Skills:
• Experience in risk analysis.
• German language skills.
• Familiarity with SAP, DMS, and TrackWise.
• Independent and proactive working style.
Work Flexibility: Up to 40% home office (2 days per week).
What’s on Offer
• A 4-month contract with a leading global pharmaceutical company.
• The opportunity to contribute to critical qualification activities in a state-of-the-art facility.
• Exposure to high-impact projects within a multidisciplinary and collaborative team.
Contract Type: Contract
Start Date: ASAP
Location: Visp, Switzerland
Workload: 100%
Duration: 4 months
Your Mission
• Oversee quality-related responsibilities for daily qualification activities on technical facilities, equipment, and systems.
• Support the development, review, and release of qualification documents.
• Approve qualification documents and assess change requests for relevance to the qualified state, including supporting and approving quality risk analyses (e.g., GMP-FMEA).
• Ensure deviations are investigated and addressed appropriately in deviation reports.
• Maintain compliance with legislation, authority guidelines, and customer expectations.
• Report relevant developments and trends to the QA Qualification Group Manager.
• Contribute to the formulation and development of qualification strategies and participate in continuous training.
• Support internal audits, customer audits, and official inspections as a QA representative.
Your Background
• Proven experience in the biotechnology or pharmaceutical industry.
• Expertise in QA Qualification, including knowledge of FAT/SAT/IQ/OQ/PQ processes.
• Proactive, with strong communication skills and the ability to work effectively in a multidisciplinary team.
• Fluency in English (spoken and written).
Beneficial Skills:
• Experience in risk analysis.
• German language skills.
• Familiarity with SAP, DMS, and TrackWise.
• Independent and proactive working style.
Work Flexibility: Up to 40% home office (2 days per week).
What’s on Offer
• A 4-month contract with a leading global pharmaceutical company.
• The opportunity to contribute to critical qualification activities in a state-of-the-art facility.
• Exposure to high-impact projects within a multidisciplinary and collaborative team.
I manage this role