Switzerland onlyAfter an onboarding period in Visp, Switzerland, the position will be based in the U.S. (East or Mid-West Coast) to support the expansion of small molecules/bioconjugation capabilities. The role will involve optimizing daily GMP operations, improving process robustness, and ensuring safe, compliant, and timely production.
Requirements
- Bachelor’s degree in a scientific or engineering field—or equivalent relevant experience and learning gained through industry roles.
- Experience working in GMP manufacturing, pharmaceutical operations, biotechnology, or a similar regulated environment.
- Ability to contribute to equipment and process introduction activities, with familiarity in areas such as FAT/SAT and qualification steps considered beneficial.
- Clear and supportive communication skills, with the ability to train and collaborate with colleagues across functions and levels.
- A practical approach to problem-solving, using structured methods to identify root causes and drive improvements.
- A proactive, organized mindset, with the ability to balance multiple activities while maintaining a commitment to safety, quality, and continuous improvement.
Benefits
- An agile career and dynamic working culture, with the opportunity to work on an international assignment
- A highly collaborative environment that fosters teamwork and inclusion
- A range of professional development programs to grow your skills and career
- An ethical workplace where tasks are carried out in accordance with relevant procedures
AU, CA + 7 more
BE, CA + 9 more
IN, CH + 2 more
United States only
United Kingdom only
Germany only
