Bioprocess Engineer for MMM MC1 DSP 80-100% (m/f/d) (Biotechnology)

Location: CH - Visp, Switzerland; fully site-based. Relocation assistance is available for eligible candidates and their families.

Company

hirify.global operates more than 30 sites across five continents and manufactures medicines and life-science products through globally connected teams.

What you will do

• Serve as the Bioprocess Engineer for downstream processing manufacturing operations, ensuring reliable execution of clinical and commercial campaigns within safety, quality, GMP, and compliance requirements.
• Act as the primary MES and manufacturing systems representative for the assigned DSP area, supporting recipe execution, troubleshooting, optimization, and continuous improvement.
• Provide first-line support for DeltaV and MES in collaboration with Operations, Automation, MSAT, QA, and Technical Support.
• Own, maintain, and review electronic batch records, manufacturing recipes, workflows, and GMP documentation.
• Lead investigations, deviations, CAPAs, and change controls related to manufacturing systems, batch execution, and process documentation.
• Support digitalization, process transfers, new product introductions, validation, and manufacturing system enhancements while improving workflow simplicity, data visibility, and manufacturing performance.

Requirements

• Master’s degree in Biotechnology, (Bio)chemical Engineering, Life Sciences, Automation, Industrial Engineering, or a related discipline; alternatively, a Bachelor’s degree with relevant biopharmaceutical manufacturing experience.
• Experience in biopharmaceutical manufacturing with a strong understanding of downstream processing and GMP requirements.
• Knowledge of Manufacturing Execution Systems, electronic Batch Records, and process automation platforms such as DeltaV.
• Experience supporting manufacturing operations, troubleshooting process and system issues, and driving continuous improvement initiatives.
• Understanding of data integrity, change management, deviation management, and GMP documentation requirements.
• Strong analytical and problem-solving skills, with the ability to manage multiple stakeholders across Operations, QA, Automation, MSAT, and Technical Services.
• Excellent communication skills in English.
• Ability to work in a fast-paced manufacturing environment with a strong focus on quality, compliance, and operational excellence.

Nice to have

• German language skills.

Culture & Benefits

• Agile career opportunities and a dynamic working culture.
• Inclusive and ethical workplace with a focus on collaboration, accountability, excellence, passion, and integrity.
• Compensation programs recognizing high performance.
• Competitive salary with lifestyle, family, and leisure benefits.