Looking for an opportunity to enhance your resume with experience working at a leader in the biopharmaceutical industry? Or are you in between jobs, open for short term projects? We might have something for you!
About the Client
The company is a leading player in the life sciences industry, with a strong presence in Switzerland and a reputation for excellence in pharmaceutical production. At this facility, they drive innovation across the entire biopharmaceutical lifecycle, offering a cutting-edge working environment in one of Europe's most important biotech hubs. Employees benefit from an international and collaborative culture, as well as a stunning location.
Job Description
We are looking for a temporary USP specialist to support and optimize large-scale upstream processing activities within a cGMP biopharmaceutical production environment. This position involves process design, automation, scale-up, and technical support for large-scale production. The role requires a strong understanding of upstream processing, compliance with GMP standards, and the ability to drive process improvements in a dynamic manufacturing environment.
Responsibilities
- Lead upstream process optimization, troubleshooting, and continuous improvement initiatives.
- Support tech transfer activities and ensure successful scale-up of upstream processes.
- Develop and maintain GMP documentation, including SOPs, deviations, and CAPAs.
- Oversee automation, bioreactor operations, and media/buffer preparation.
- Ensure compliance with GMP, safety, and quality requirements in all production activities.
- Collaborate with cross-functional teams, including quality, validation, and engineering.
- Conduct process monitoring, data analysis, and reporting to drive operational efficiency.
- Provide technical expertise for process development and production teams.
Requirements
- University degree (BSc, MSc, or higher) in Biotechnology, Bioprocess Engineering, or Life Sciences.
- 3-6 years of experience in a GMP-regulated biopharmaceutical environment.
- Strong knowledge of bioreactor operation, media/buffer preparation, and process control.
- Experience with process automation and troubleshooting (DeltaV or similar) is a plus.
- Fluency in English; German is a plus.
Benefits
- Temporary contract through Oxford Global Resources.
- Insurance and pension.
