On-Site DSP Bioprocess Engineer: Shape Life-Saving Therapies

Lonza; Oberwallis; On-site; Vertraulich; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Competitive compensation

Lifestyle and family benefits

Job summary

Lonza in Visp, Switzerland, is seeking a Bioprocess Engineer for DSP operations (M/MM 80-100%). The role focuses on GMP-compliant DSP campaigns, MES ownership, and DeltaV support to ensure high-quality manufacturing of therapies.

You will collaborate with Operations, MSAT, QA, Automation and Technical Services to maintain data integrity and drive continuous improvement in a fast-paced biotech environment.

Qualifications

• Master’s Degree in Biotechnology, (Bio)chemical Engineering, Life Sciences, Automation, Industrial Engineering, or a related discipline; Bachelor’s with relevant experience accepted.
• Experience in biopharmaceutical manufacturing with GMP requirements.
• Knowledge of MES, eBR, and DeltaV automation platform.
• Experience supporting manufacturing operations and driving improvements.

Responsibilities

• Serve as Bioprocess Engineer for DSP manufacturing, ensuring GMP-compliant campaigns.
• Act as MES and manufacturing systems representative for DSP area.
• Provide first-line DeltaV and MES support with Operations and QA.
• Own and review eBRs, workflows, and GMP docs for compliance and efficiency.
• Lead investigations, deviations, CAPAs, and change controls.
• Drive digitalization to simplify workflows and improve data visibility.
• Support process transfers, new product introductions, and validation efforts.
• Interface between Production, Automation, MSAT, QA and Technical Services.

Skills

Analytical thinking

Problem solving

Cross-functional collaboration

English communication

Education

Master’s Degree in Biotechnology or related field

Bachelor’s Degree with biopharmaceutical manufacturing experience

Tools

DeltaV

MES

eBR

Job description

Lonza in Visp, Switzerland, is seeking a Bioprocess Engineer for DSP operations (M/MM 80-100%). The role focuses on GMP-compliant DSP campaigns, MES ownership, and DeltaV support to ensure high-quality manufacturing of therapies.

You will collaborate with Operations, MSAT, QA, Automation and Technical Services to maintain data integrity and drive continuous improvement in a fast-paced biotech environment.