Process Validation Engineer
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-07-24
Listing for:
F. Hoffmann-La Roche AG
Full Time
position Listed on 2026-07-24
Job specializations:
-
Engineering
Process Engineer, Quality Engineering, Validation Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Baseltime type:
Full time posted on:
Posted 8 Days Agotime left to apply:
End Date:
May 19, 2026 (5 days left to apply) job requisition :
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 Ready to make a difference? Apply now!
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