Internship in Sensor & Cartridge Operations Rotkreuz with focus on MSAT Process Management & Improvement (6-12 Months)

Rotkreuz, SwitzerlandFull-timePosted Jul 31, 2026

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

The Manufacturing Science & Technology (MSAT) team, part of Sensor & Cartridge (S&C) Operations, is dedicated to supporting the manufacturing and quality control of Roche Blood Gas and Electrolyte (BG&E) Sensors and Reagents. These systems are a critical part of first-frontier diagnostics, delivering fast, reliable results in patient-critical settings like the intensive care unit, emergency room, and operating room. We are a dynamic and interdisciplinary team committed to improving product quality and driving continuous improvement.  Within our Continuous Improvement scope, this position focuses on deep-dive data analysis, yield experiments, and line simulations to unlock production potential. 

We are seeking a highly motivated intern to join our team in Rotkreuz, Switzerland.

In this role, you will be a key contributor to our Process Improvement (PI) initiatives within BG&E operations. Your work will center on deep-dive data analysis (costs, yield, analytics, production simulation) to uncover optimization opportunities like barriers to execution or throughput bottlenecks.

The Opportunity
As an MSAT intern, you will gain hands-on experience in the medical device industry by contributing to critical analytical and optimization tasks. Your work will directly impact our  ability to produce life-saving diagnostic systems.

Your responsibilities will include:

  • Process Improvement (PI): Analyzing production processes and associated data from various angles, such as manufacturing costs, yield experiments, or QC analytics. Reporting findings and conclusions to drive decisions.

  • Lean Development: Contributing to the development of new and existing ideas for process improvements, helping to shape them according to Lean Manufacturing principles and implementing them under GxP conditions.

  • Production Simulation:  Running simulations of our modern, highly automated production line to identify throughput bottlenecks and extract the key levers that drive throughput during production rampup. Translating outputs into concrete, actionable recommendations in close collaboration with production.

  • Risk Analysis: Supporting process risk analyses (pFMEA) by preparing operational inputs, documenting technical outcomes, and assisting the team in systematically identifying and mitigating risks.

  • Document & Change Management: Creating and managing GxP-compliant documents (manufacturing and QC process documentation, work instructions) with a focus on integrating sustainability into documentation practices. Supporting necessary regulatory change management processes.

  • Knowledge Documentation: Ensuring project knowledge is well-documented in Wiki articles for easy access and retention.


Who You Are

You are a current Bachelor or Master student (or graduated within the last 12 months) in life sciences, chemistry, process engineering, biotechnology, applied informatics, or a related field.You are highly analytical, enthusiastic about operational excelence, and eager to experience a real-world manufacturing environment through the lens of continuous improvement. 

Additionally, you bring:

  • Excellent collaboration skills to coordinate tasks with both internal and external partners.

  • A strong love for numbers, data charts, and structured data analysis.

  • A strategic mindset, a strong sense of timeline ownership, and an entrepreneurial spirit.

  • An eye for detail and an appreciation for precise documentation in alignment with GDP/GMP guidelines.

  • An interest in working within a highly regulated medical sector and navigating structured operational environments.

  • Proficiency in both English and German.


Start: as soon as possible.

If you are ready to make a significant impact and gain valuable experience in the medical diagnostics field, please submit your application (CV and cover letter).

We look forward to hearing from you!
 

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.


Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

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