Bioprocess Engineer, Deviation Investigation 80%-100% (m/w/d) — Lonza
- Location
- Visp
- Contract
- full-time
- Posted
- 3 days ago
Role overview
Bioprocess Engineer, Deviation Investigation 80%-100% (m/w/d)
The actual location of this job is in Visp, Switzerland.
Join a dedicated team at the forefront of GMP manufacturing excellence, where you will lead critical deviation investigations that help ensure the quality, safety, and reliability of life-changing therapies.
- Bioprocess Engineer, Deviation Investigation 80%-100% (m/w/d)
- The actual location of this job is in Visp, Switzerland.
Application process
- This is an exciting opportunity to apply scientific expertise, collaborate across multiple functions, and drive continuous improvement in a highly regulated biopharmaceutical environment.
- now.
- Lonza is a global leader in pharma and biotech manufacturing.
- The company operates major production facilities in Visp (Valais), Basel, and Stein (Aargau), Switzerland.
Company and context
- Strong organizational skills with the ability to manage multiple priorities, drive timely execution, and maintain high-quality documentation standards. About Lonza
- At Lonza, our people are our greatest strength.
- With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
- Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
- Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
- Innovation thrives when people from all backgrounds bring their unique perspectives to the table.
- At Lonza, we value diversity and are committed to creating an inclusive environment for all employees.
- If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
- Ready to shape the future of life sciences?
Additional details
- Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
- Professional development through exposure to complex GMP investigations, inspection readiness activities, and continuous improvement initiatives. A variety of benefits dependent on role and location.
- The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits
- Contribute to deviation reduction initiatives, recurring issue analysis, workload tracking, and the continuous improvement and standardization of investigation practices across the team. What we are looking for:
- Strong organizational skills with the ability to manage multiple priorities, drive timely execution, and maintain high-quality documentation standards.
Notes and original content
- What you will get:
- Professional development through exposure to complex GMP investigations, inspection readiness activities, and continuous improvement initiatives.
- A variety of benefits dependent on role and location.
- What you will do:
- Contribute to deviation reduction initiatives, recurring issue analysis, workload tracking, and the continuous improvement and standardization of investigation practices across the team.
- What we are looking for:
- About Lonza
Questions about this listing
What salary does Lonza offer for this role?
Lonza lists CHF 68'000 - 92'000 gross per year for this position in Visp. 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 Lonza 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 Lonza 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 Valais?
EU/EFTA residents living in the border zone of the country adjoining Canton Valais 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 Valais's cantonal migration office or with HR during the application.
How do I apply for this position at Lonza?
Use the "Apply now" button on this page — it links directly to Lonza's original listing at lonza.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
