DSP Bioprocess Engineer

Location: Visp, Switzerland
Contract Duration: Until 31 January 2027
Work Environment: On-site | GMP Biopharmaceutical Manufacturing

About the Role

We are looking for an experienced DSP Bioprocess Engineer to support commercial and clinical manufacturing activities within a leading biopharmaceutical environment in Visp.

In this role, you will act as a technical subject matter expert for Downstream Processing (DSP), supporting manufacturing operations, process improvements, troubleshooting activities, and technology transfers. You will work closely with Manufacturing, Quality, Engineering, and cross-functional teams to ensure safe, compliant, and reliable production according to cGMP standards.

Key Responsibilities

• Support the planning, execution, monitoring, and documentation of DSP manufacturing campaigns.
• Act as the manufacturing SME for assigned products and processes.
• Provide technical support during batch execution, process monitoring, troubleshooting, and issue resolution.
• Drive process improvements to enhance safety, quality, efficiency, and robustness.
• Lead and support investigations, deviations, CAPAs, change controls, and risk assessments.
• Support commissioning, qualification, operational readiness, and technology transfer activities.
• Develop and maintain GMP documentation, including SOPs, manufacturing instructions, and risk assessments.
• Support training activities for manufacturing teams.
• Collaborate with Manufacturing, Quality Assurance, Engineering, and other stakeholders.

Your Profile

• Bachelor’s or Master’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related field.
• Experience in biopharmaceutical manufacturing, DSP, process engineering, MSAT, or technical operations.
• Strong understanding of cGMP requirements and regulatory expectations.
• Experience with deviations, CAPAs, change controls, risk assessments, and validation activities.
• Strong troubleshooting and problem-solving skills.
• Excellent communication and stakeholder management abilities.
• Ability to work effectively in a dynamic and highly regulated manufacturing environment.

Project Details

Location: Visp, Switzerland
Contract: Until 31 January 2027
Working model: Fully on-site

This is a great opportunity to contribute to the production of innovative medicines while working in a highly experienced biopharmaceutical manufacturing team.

Interested? Apply today or get in touch to learn more about this opportunity.