Bioprocess Engineer USP/DSP (Microbial)/BioConjugates
Lonza
Visp, Switzerland
What you’ll do:
- Ensure timely execution of operational activities for clinical and commercial manufacturing while maintaining safety and quality standards.
- Serve as a subject matter expert in the design, commissioning, and qualification of new facilities, as well as preparation, execution, cleaning, and changeovers in assigned areas.
- Lead one or more specialized areas, such as: Upstream processing (e.g., inoculation, main cultivation, or primary recovery); downstream processing; Bio-Conjugates
- Perform manufacturing tasks in compliance with cGMP guidelines, including batch execution, test result evaluations, equipment troubleshooting, and resolution recommendations.
- Review production documentation, address deviations and change requests, and implement CAPAs to maintain high-quality GMP standards.
- Participate the development and review of automation recipes for equipment and facility components.
- Train production personnel on assigned products.
- Actively participate in audits and customer visits.
What we’re looking for:
- Master's degree or equivalent experience in Biotechnology, Biochemical Engineering, Biochemistry, Process Engineering, or a related Life Science field (or a Bachelor's degree with relevant pharmaceutical production experience).
- Expertise in Upstream, Downstream processing, or Bio-conjugation technology.
- Experience in bio-manufacturing and/or scaling up a biopharmaceutical facility, with cGMP experience being an advantage.
- Excellent English communication skills; German proficiency is a plus.
- An organized and goal-oriented approach to work, with a willingness to consider new ideas, strong motivation, and a problem-solving approach.
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