Bioprocess Development Scientist

Bioprocess Development Scientist
  • posted job: 2025-07-08
  • Zurich
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  • Job Country: Switzerland
  • Job Industry: Biotechnology & Life Sciences
  • Job Profile: Process Development Scientist
  • Training Duration: Not Required
  • Number of Jobs Opening: 55
  • Salary: 170000 ( 170000 Per Month)
  • Job Type: Full Time
  • Visa: Provided by company
  • Food: Provided by company
  • Accommodation: Provided by company
  • Air ticket: Provided by company
  • Medical Insurance: Provided by Company
  • Commuting to job location: Provided by company
  • Required Experience: Not Required
  • Minimum Education Level: Not Required
  • Primary Language Requirement: English
  • Level of Language: Beginner
  • Secondary Language Requirement: Not Required
  • Employee Acceptance: International
  • Work Location: Work from Home (WFH) /Remote Work
  • Hiring Need: Immediate

Job Description:

A Bioprocess Development Scientist in Zurich is responsible for designing, optimizing, and scaling up biological production processes used in manufacturing vaccines, proteins, or cell therapies. This role focuses on upstream (fermentation, cell culture) and/or downstream (purification, filtration) processes. The scientist evaluates critical process parameters, ensures regulatory compliance, and contributes to technology transfers to manufacturing sites. In Zurich’s biotech manufacturing landscape, the role involves working with automated systems, bioreactors, and chromatography platforms. The scientist also participates in troubleshooting, process validation, and continuous improvement initiatives. Proficiency in bioprocessing technologies, GMP standards, and data analysis tools is required. The ability to work in a team and communicate effectively across departments is essential.

Job Requirement:

  • Demonstrated experience in laboratory research, scientific data analysis, and technical reporting.

  • Proficiency in using laboratory equipment, software tools for data interpretation, and bioinformatics platforms.

  • Familiarity with GMP, GLP, GCP, and other regulatory compliance standards applicable to clinical and laboratory environments.

  • Strong documentation and record-keeping skills in accordance with industry standards.

  • Ability to design, execute, and troubleshoot experiments and assays independently or in a team.

  • Excellent written and verbal communication skills for preparing research documentation and collaborating across departments.

  • Detail-oriented with strong analytical thinking, problem-solving, and organizational capabilities.

  • Adaptability to fast-paced, collaborative, and evolving research and clinical settings.

  • Understanding of ethical research practices and commitment to maintaining data integrity and confidentiality.

  • Previous experience with clinical trials, product development, or regulatory processes is considered an advantage.

  • Ability to work with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing.

  • Good time management skills and ability to meet tight project deadlines.

  • Fluency in English is mandatory; knowledge of German or French is a plus for Swiss workplaces.

  • Willingness to undergo ongoing training and certification as required by the organization.

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Kameda Medical Center
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Hitachi
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Honda
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Mazda
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Schneider Electric