Senior Commissioning & Qualification Engineer Sisslerfeld (a), 100% — Bachem AG
- Location
- Stein AG
- Contract
- full-time
- Posted
- Yesterday
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
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
- Proven experience in international CAPEX projects (medium to large scale, complex requirements) Extensive C&Q expertise in areas such as: Biologics/Drug Substance, Drug Product Small Molecules
- Packaging, warehousing, GMP & non‑GMP infrastructure Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.) Ideally experience with KNEAT Gx
- Deep understanding of project management, PQS/EM compliance, and interfaces with Quality
- Excellent communication, collaboration, and leadership skills
- Analytical thinking and financial acumen to derive sustainable, efficient solutions
Application process
- We look forward to receiving your complete application documents via our application portal.
- Learn more about the Bachem Group and get inspired by our exciting work environment!
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
Additional details
- 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.
- Proven experience in international CAPEX projects (medium to large scale, complex requirements) Extensive C&Q expertise in areas such as: Biologics/Drug Substance, Drug Product
- Packaging, warehousing, GMP & non‑GMP infrastructure Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.) Ideally experience with KNEAT Gx
- Confident working style in global, culturally diverse teams
Notes and original content
- Your tasks:
- Your profile:
- Proven experience in international CAPEX projects (medium to large scale, complex requirements)
- Extensive C&Q expertise in areas such as:
- Biologics/Drug Substance, Drug Product
- Small Molecules
- Packaging, warehousing, GMP & non‑GMP infrastructure
- Automation systems & new technologies
- Strong knowledge of global regulations (FDA, EMA, ICH, ISPE Integrated Commissioning & Qualification, etc.)
- Ideally experience with KNEAT Gx
Questions about this listing
What salary does Bachem AG offer for this role?
Bachem AG lists CHF 99'500 - 151'000 gross per year for this position in Stein AG. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Bachem AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Bachem AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Aargau?
EU/EFTA residents living in the border zone of the country adjoining Canton Aargau can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Aargau's cantonal migration office or with HR during the application.
How do I apply for this position at Bachem AG?
Use the "Apply now" button on this page — it links directly to Bachem AG's original listing at careers.bachem.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
