GMP Bioprocess Engineer – Relocation Support (Visp)

Lonza Group Ltd.; Oberwallis; On-site; CHF 110,000 - 150,000; Full time

Benefits offered by this job

Agile career path

Inclusive work environment

Diverse development opportunities

Benefits in Visp

Job summary

Lonza Group Ltd. in Visp, Switzerland, is seeking a Bioprocess Engineer (m/f/d) 80%-100% to plan, execute, and improve GMP bioprocesses onsite. Relocation support is available and remote work is not offered.

You will collaborate with Operations, MSAT, Quality, and Engineering to ensure high-quality production of life-changing therapies. The role emphasizes hands-on GMP manufacturing, documentation, and continuous improvement with Lean Six Sigma methods.

Qualifications

• Bachelor's or Master's degree in Biotechnology, Bioprocess Engineering, Chemical Engineering, Life Sciences, or a related field.
• Experience in a GMP-regulated biotech/pharma environment.
• Strong knowledge of biotechnological manufacturing processes and GMP documentation.

Responsibilities

• Plan, execute, and document GMP manufacturing campaigns with Operations Head.
• Provide technical and organizational support for GMP production including training production personnel.
• Create, optimize, and review GMP documentation (EBRs, SOPs, work instructions).
• Handle deviations, change controls, and CAPAs with a first-time-right approach.
• Monitor KPIs and implement improvements using Lean, Six Sigma, Kaizen.
• Ensure equipment and areas stay qualified and compliant; participate in on-call rotations.
• Execute and optimize cleaning processes and perform risk assessments related to SHE, O.E. and Cleaning Validation.

Skills

GMP manufacturing

Bioprocess engineering

Analytical skills

English communication

Education

Bachelor's or Master's in Biotechnology/Bioprocess Engineering/Chemical Engineering/Life Sciences

Job description

Lonza Group Ltd. in Visp, Switzerland, is seeking a Bioprocess Engineer (m/f/d) 80%-100% to plan, execute, and improve GMP bioprocesses onsite. Relocation support is available and remote work is not offered.

You will collaborate with Operations, MSAT, Quality, and Engineering to ensure high-quality production of life-changing therapies. The role emphasizes hands-on GMP manufacturing, documentation, and continuous improvement with Lean Six Sigma methods.