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USP and DSP Scientist (Separate Roles)

USP and DSP Scientist (Separate Roles)

LocationVevey, Switzerland
Business SectorBiotechnology
Contact email
Job ref24516
Publishedabout 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
     

PROFILE

  • 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!