MSAT Bioconjugates Process Expert — Onsite in Visp

CH12 Lonza AG; Oberwallis; On-site; CHF 120,000 - 160,000; Full time

Benefits offered by this job

Relocation assistance

On-site role in Visp

Job summary

Lonza Group Ltd. in Visp, Switzerland, is seeking a MSAT Bioconjugates Process Expert to join the Bioconjugates Manufacturing team on-site in Visp.

This 80-100% role focuses on delivering process know-how, technology transfer, and continuous improvement to support biopharma API manufacturing. You will drive process optimization, lead troubleshooting on the shop floor, and collaborate with Process Development, Operations, QA and QC to ensure quality and compliance.

Qualifications

• Master’s degree or PhD in Bioconjugation, Biotechnology, Chemical Engineering or related field.
• Experience with bioconjugation methodologies and biopharma manufacturing.
• Hands-on downstream processing with chromatography and filtration.

Responsibilities

• Deliver process know-how and operational excellence for biopharma API manufacturing.
• Coordinate successful technology transfer with Process Development, Operations, QA and QC.
• Own and support change control activities to maintain compliant manufacturing processes.
• Provide manufacturing support during production campaigns and lead shop-floor troubleshooting.
• Drive process optimization through data analysis and CPV/APQR documentation with data management teams.
• Identify and implement workflow and asset improvements through continuous improvement projects.
• Act as SME, supporting operational excellence and knowledge sharing across the organization.

Skills

Bioconjugation

Process transfer

cGMP manufacturing

Analytical thinking

Cross-functional collaboration

Education

Master’s degree (Bioconjugation/Biotech/Chemical Eng)

PhD preferred

Tools

Chromatography

Filtration

Job description

Lonza Group Ltd. in Visp, Switzerland, is seeking a MSAT Bioconjugates Process Expert to join the Bioconjugates Manufacturing team on-site in Visp.

This 80-100% role focuses on delivering process know-how, technology transfer, and continuous improvement to support biopharma API manufacturing. You will drive process optimization, lead troubleshooting on the shop floor, and collaborate with Process Development, Operations, QA and QC to ensure quality and compliance.