MSAT Bioconjugates Process Expert
📍 CH - Visp
Role and responsibilities
Deliver process know-how, scientific expertise and operational excellence for biopharma API manufacturing. Ensure successful process technology transfer and manufacturability by collaborating with cross-functional teams including Process Development, Operations, QA and QC. Own and support change control activities to maintain compliant and efficient manufacturing processes. Provide manufacturing support during production campaigns and lead process troubleshooting activities on the shop floor. Drive process optimization through data analysis and preparation of CPV and APQR documentation in partnership with data management teams. Identify and implement workflow, process and asset improvements through innovation and continuous improvement projects. Act as a technical subject matter expert, supporting operational excellence and knowledge sharing across the organization.
Team / description
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees.
Qualifications and Skills
Master’s degree or PhD (preferred) in Bioconjugation, Biotechnology, Chemical Engineering or a related scientific discipline, with a focus on organic chemistry.
Significant industry experience in bioconjugation methodologies, biopharma manufacturing and/or process development, ideally within bioconjugates.
Hands-on experience with downstream processing, including chromatography and filtration technologies.
Strong analytical and problem-solving skills with the ability to interpret complex data and make sound technical decisions.
In-depth understanding of bioprocess technologies and practical cGMP manufacturing experience.
Excellent communication and interpersonal skills with the ability to work effectively in cross-functional teams.
Fluent English language skills; German language knowledge is an advantage. Creative, agile and open-minded approach to challenges.