Project Engineer – CQV & Equipment Changes (m/w/d)

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.
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  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 ASAP? Apply Now !