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Process Validation Engineer

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: Roche
Full Time position
Listed on 2026-07-27
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer, Validation Engineer
  • Manufacturing / Production
    Quality Engineering, Manufacturing Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 120000 - 180000 CHF Yearly CHF 120000.00 180000.00 YEAR
Job Description & How to Apply Below

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 Process Validation Chapter is a part of the Basel Drug Substance Manufacturing organization and is responsible for supporting the validation of the production process during routine commercial manufacturing, technology transfers, process optimizations and for leading implementation of new technologies to drive manufacturing efficiencies.

The Opportunity:

You develop, execute, and implement process validation strategies and concepts. Furthermore:

  • Support technical process technology transfers e.g. from development to commercial scale manufacturing
  • End-to-end ownership of validation deliverables from conceptual work and plan creation to the implementation of necessary training and coordination of samples, to the interpretation of results and preparation of validation reports
  • Planning and coordination of troubleshooting activities in cooperation with the pilot laboratories, production and the quality department
  • Processing of deviations and changes according to GMP guidelines
  • Support for optimization projects
Who you are:

You hold a university degree (or equivalent training/experience) in a scientific or technical field. Preferably in the field of biotechnology, bioprocess engineering, or (bio) chemical engineering. Furthermore:

  • Experience in working in a GMP environment and ideally in the planning and implementation of process validation or characterization studies
  • You should be a team player who can work independently in a dynamic environment and enjoys collaborating with diverse interfaces
  • Ability to adapt to a rapidly changing environment with changing priorities and to respond flexibly to requests
  • Very good (also intercultural) communication skills
  • Fluent in German and English
  • Bioprocess knowledge and/or project management skills are a plus
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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