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USP/DSP Scientist – Clinical Manufacturing
Vevey, Switzerland – Full-time, 4-month contract (possibility of extension)
Company Description
This leading biopharmaceutical company, based in Vevey, Switzerland, is at the forefront of innovation in large-scale biologics manufacturing. With a strong focus on supporting early-phase clinical programs, the site specializes in producing materials for Phase I and II clinical trials using state-of-the-art technologies and scalable bioprocessing systems.
Job Description
As an Upstream Process (USP) Scientist or Downstream Process (DSP) Scientist, you will play a vital role in supporting clinical manufacturing operations for biologics ranging from 200L to 2000L scale. In these roles, you will support the execution of pre-clinical and clinical campaigns, ensuring compliance with GMP and safety standards while contributing to the integration of new technologies and continuous improvement of bioprocesses.
Working in close collaboration with cross-functional teams - such as Production, QA, QC, and Engineering - you will be responsible for technical execution, batch documentation, deviation management, and supporting process implementation for either cell culture (USP) or purification (DSP).
Key Responsibilities:
* Perform Electronic Batch Record (EBR) reviews using MES (Manufacturing Execution System)
* Lead and close deviations, investigations, CAPAs, and critical control point (CCP) actions in alignment with the site’s quality plan
* Ensure compliance with GMP, safety protocols, and internal quality standards
* Maintain an up-to-date training plan and adhere to individual training requirements
* Proactively report unexpected events and ensure full traceability of assigned tasks
* Follow site EHS procedures and immediately report hazardous conditions or behaviors
* Wear and maintain proper use of PPE and safety devices
* Suggest improvements and actively contribute to a culture of safety and quality
* PhD in Chemistry, Biology, Biotechnology, or a related field with 1–2 years of industry experience OR MSc/Engineering degree with 4–5 years of relevant experience OR Technical degree with 10+ years of relevant experience in GMP manufacturing
* Strong expertise in either: USP: Fed-batch and/or perfusion cell culture or DSP: Chromatography, filtration, and purification operations
* Working knowledge of GMP and BPF regulations
* Proficiency in MES and the ability to conduct electronic batch record reviews
* Strong communication and teamwork skills, with the ability to collaborate across departments (Production, QA, QC, Tech Ops)
* English fluency required; French is a strong plus
* Familiarity with TrackWise, SAP, LIMS, and standard office IT tools
* Prior experience in clinical or commercial pharmaceutical production in either upstream or downstream roles
* Demonstrated experience in deviation/CAPA management
Additional Insights:
* Contract Type: 4-month contract with strong potential for extension
Interested?
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or reach out directly at
+41445514407 to learn more.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Manufacturing and Science
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