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 ASAP? Apply Now !