Bioprocess Engineer USP/DSP(Microbial)/BioConjugates

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Lonza

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.

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.

Don't forget to mention EuroPharmaJobs when applying.

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