Bioprocess Engineer – Up/Downstream & GMP (Switzerland)

PrimeIT Switzerland; Basel; On-site; CHF 110,000 - 160,000; Full time

Benefits offered by this job

Permanent contract

Five weeks paid vacation

Annual training plan

Job summary

PrimeIT Switzerland is seeking a Bioprocess Engineer (100%) in Switzerland to develop, optimize, and scale-up upstream (cell culture) and downstream (purification) processes, and to support technology transfer between development and manufacturing.

You will implement process monitoring, data analysis, and continuous improvement initiatives, and ensure GMP compliance and regulatory alignment across all process activities.

Qualifications

• Degree in biotechnology, biochemistry, chemical engineering, or related field.
• Professional experience in upstream and downstream bioprocess engineering.
• Strong knowledge of bioreactors, chromatography, and filtration systems.
• Familiarity with GMP, regulatory expectations, and process validation.
• Problem-solving mindset, team spirit, and ability to work in a multidisciplinary environment.

Responsibilities

• Develop, optimize, and scale-up upstream (cell culture) and downstream (purification) processes
• Contribute to technology transfer activities between development and manufacturing sites
• Implement process monitoring, data analysis, and continuous improvement initiatives
• Support troubleshooting and root cause analysis for process deviations
• Ensure compliance with GMP standards and regulatory guidelines in all process-related activities

Skills

Bioprocess engineering

Upstream processing

Downstream processing

GMP compliance

Problem-solving & teamwork

Education

Biotechnology/Biochemistry/Chemical Engineering degree

Tools

Bioreactors

Chromatography systems

Filtration systems

Job description

PrimeIT Switzerland is seeking a Bioprocess Engineer (100%) in Switzerland to develop, optimize, and scale-up upstream (cell culture) and downstream (purification) processes, and to support technology transfer between development and manufacturing.

You will implement process monitoring, data analysis, and continuous improvement initiatives, and ensure GMP compliance and regulatory alignment across all process activities.