Together with a leading biotech company, we are looking for a QA Qualification Engineer to join their team in Visp. This role is ideal for a proactive professional with experience in pharmaceutical or biotechnology environments, looking to contribute to high-quality standards in a global setting.
Key Responsibilities:
- Oversee all quality-related aspects of daily qualification activities for technical facilities, equipment, and systems.
- Develop, review, approve, and release qualification documents (FAT/SAT/IQ/OQ/PQ).
- Assess and approve change requests to maintain the qualified state condition, supporting and approving quality risk analyses (e.g., GMP-FMEA).
- Ensure deviations are properly investigated and documented in deviation reports.
- Stay up to date with GMP legislation, authority requirements, and customer expectations to ensure compliance.
- Provide updates on trends and developments to the Group Manager QA Qualification.
- Actively 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.
Key Requirements:
- Experience in a biotechnology or pharmaceutical environment
- Previous experience in QA Qualification
- Strong knowledge of FAT, SAT, IQ, OQ, PQ
- Proactive mindset with strong communication skills and the ability to work in a multidisciplinary team
- Experience in risk analysis
- Knowledge of SAP, DMS, and TrackWise
- Independent, proactive working style
Practicalities:
Location: Visp, Switzerland (Hybrid)
Start Date: ASAP (Flexible)
Duration: full time, 6 months (High possibility of extension)
Languages: English, German
This is an excellent opportunity to join a dynamic team and contribute to high-impact projects in one of Switzerland’s leading pharmaceutical hubs!
Are you interested, or know someone that might be? Then apply today below with your CV or send an email to f.karampina@panda-int.com!