Senior Commissioning & Qualification Engineer Sisslerfeld (a), 100% — Bachem AG
CHF 68'000 - 103'000
Bachem AG · Stein AG (AG)
- Location
- Stein AG
- Contract
- full-time
- Posted
- 38 days ago
SalaryCHF 68'000 - 103'000
Role overview
The Bachem Group is investing in a new site in Sisslerfeld in Northwestern Switzerland.
This step is part of the long-term strategy to expand production capacity by the end of the decade.
The new production site will play a central role in achieving these goals.
- The Bachem Group is investing in a new site in Sisslerfeld in Northwestern Switzerland.
- This step is part of the long-term strategy to expand production capacity by the end of the decade.
- Completed degree in engineering, natural sciences, or a related field At least 10 years of professional experience in the pharmaceutical or biopharmaceutical industry <li style="color:#004080;margin-top:0.0cm;margin-rig
Key requirements
- Completed degree in engineering, natural sciences, or a related field At least 10 years of professional experience in the pharmaceutical or biopharmaceutical industry <li style="color:#004080;margin-top:0.0cm;margin-rig
Company and context
- The design phase of the project offers you unique opportunities to shape the future organization.
- We are looking for an experienced and dedicated Commissioning & Qualification (C&Q) Engineer (a) , 100% to support our global capital projects and play a key role in the standardization and further development of C&Q processes across our international network.
- In this role, you will be responsible for the successful planning, execution, and management of C&Q activities – from concept to handover – and will contribute your expertise to a wide range of projects worldwide.
- Your tasks: Leadership of C&Q activities within multidisciplinary large capital projects Coordination and management of C&Q‑related deviations and changes within defined timelines and in compliance with required quality standards Responsibility for budget, schedule, prioritization, resources, and the quality of C&Q execution Analysis of options, planning of execution strategies, and development of detailed C&Q schedules Preparation of tender documents, support in procurement processes, and cost estimation Ensuring a smooth handover to Operations and Quality Risk management, including the derivation of proactive measures in case of deviations Management and onboarding of the C&Q team, including external partners Responsibility for training C&Q teams and ensuring adherence to internal standards Clear, structured, and audience‑appropriate communication with all stakeholders Close collaboration with global sites to harmonize C&Q standards and digital processes Support in supplier evaluation and coaching of local SMEs Active promotion of lean and agile methods within engineering and C&Q contexts Further development of digital tools (e.g., Veeva), interfaces, and templates Technical review activities in CAPEX projects Participation in or leadership of international teams in GMP engineering, C&Q, and global initiatives
Additional details
- Your profile: Completed degree in engineering, natural sciences, or a related field At least 10 years of professional experience in the pharmaceutical or biopharmaceutical industry <li style="color:#004080;margin-top:0.0cm;margin-rig
