Location | Vevey, Switzerland |
---|---|
Business Sector | Biotechnology |
Contact email | |
Job ref | 24516 |
Published | about 19 hours ago |
We are currently looking for a USP and DSP Scientist (in separate roles) to join our major biopharmaceutical client in Vevey, Switzerland.
In both roles, you will contribute to large-scale manufacturing operations (ranging from 200L to 2000L) for the production of materials, supporting pre-clinical and clinical Phase I/II studies, laboratory activity support, and implementation of new technologies
RESPONSIBILITIES
Perform Electronic Batch Review (EBR) in MES
Lead and close deviations, investigations, CCP actions, and CAPAs as per plan
Ensure adherence to quality standards, GXP regulations, and safety protocols
Maintain an up-to-date training plan
Report unexpected events as soon as they occur
Maintain full compliance and traceability in all assigned activities
Follow all EHS rules applicable to workplace activities
Identify and immediately report hazardous situations (for self, co-workers, or the environment)
Cease activities if EHS risks are not properly controlled
Wear personal protective equipment (PPE) and use safety devices correctly
Suggest improvements and take necessary actions to prevent exposure to risks
Provide feedback on observed risky behaviors
PhD in Chemistry, Biology, or Biotechnology (or equivalent) with 1-2 years of relevant industry experience…
OR M.Sc/Engineering degree with 4-5 years of relevant industry experience
OR… Technical degree with 10+ years of relevant industry experience
English a must, French a plus
Strong expertise in Upstream (fed-batch and perfusion) OR Downstream Processing (Chromatography, filtration)
Proficiency in MES – ability to conduct EBR reviews
Knowledge of BPF and GMP regulations
Familiarity with IT tools such as Pack Office, Trackwise/SAP, MES, LIMS (a plus)
Strong teamwork and communication skills across different stakeholders (Managers, Unit Managers, Scientists, Technicians, and other departments like Production, QC, QA)
Preferred experience: USP/DSP clinical and/or commercial pharmaceutical production
PRACTICALITIES
Location: Vevey
Start date: ASAP (flexible)
Duration: 12 months minimum with high likelihood of extension
Interested? Know someone that could be? Don't hesitate to reach out on v.niesov@panda-int.com to find out more!