About Techfirm Engineering
Techfirm Engineering supports leading life sciences companies across Switzerland with specialized engineering expertise. Our teams deliver on-site solutions for complex technical challenges in biopharma environments.
Your Role
For a key project in the Visp region, we seek a Project Engineer with 6–10 years of experience to handle technical problem-solving, equipment changes, and CQV (Commissioning, Qualification, Verification) activities. You will ensure seamless execution while collaborating across engineering, production, and quality teams.
Key Responsibilities
- Resolve complex technical issues related to equipment modifications and process improvements.
- Lead CQV activities for new or upgraded equipment, including authoring IQ/OQ/PQ protocols, risk assessments (FMEA), and FAT/SAT execution.
- Coordinate cross-functional teams (engineering, QA, production, EHS) for change control, deviations, and CAPAs in GMP settings.
- Document changes, perform data analysis/gap assessments, and support vendor supervision during installations.
- Ensure regulatory alignment (cGMP/Annex 15) through requalifications and lessons learned reviews.
Your Profile
- Engineering degree (mechanical, chemical, or process engineering preferred).
- 6–10 years of relevant experience in CQV, equipment changes, or technical troubleshooting in pharma/biotech.
- Strong problem-solving skills and hands-on mentality.
- Fluent in German (primary) and English for technical communication.
Why Techfirm Engineering?
- Work on impactful projects with a major industry player.
- Dynamic environment fostering technical expertise and career growth.
- Competitive compensation and team-oriented culture.
Ready to tackle challenging engineering tasks? Apply online using the form below. Please note that only applications matching the job profile will be considered.
Work locationVisp, Switzerland