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Senior MSAT Process Expert

Senior MSAT Process Expert

LocationVisp, Switzerland
Business SectorBiotechnology
Contact email
Job ref23564
Publishedabout 2 months ago
Senior MSAT Process Expert

We are looking for a Senior Process Expert to join our MSAT (Manufacturing Science & Technology) Team at our state-of-the-art Ibex site in Visp, Switzerland.

In this role, you will play a critical part in the successful transfer, scale-up, supervision, and optimization of biopharma processes, acting as a senior expert in process science and manufacturing.

Key Responsibilities
  • Lead cross-functional teams as a process expert for technology transfers, process design, up-scaling, and timely implementation at manufacturing scale. This includes managing the entire lifecycle of assigned projects from planning through to project completion, aligned with project management goals.
  • Serve as the interface between the process donor (customer, process development) and operations, ensuring process scalability and manufacturability.
  • Secure success during technology transfer by applying formal processes and tools to manage information transfer, process-related risks, and change control.
  • Resolve process issues during manufacturing while considering all regulatory requirements.
  • Execute GMP risk analysis for manufacturing processes.
  • Act as the MSAT process expert in capital investment projects, contributing to the building and commissioning of manufacturing units and delivering all process-specific input (e.g., block-flow diagrams, media and buffer lists, critical parameter lists).
  • Implement manufacturing processes in the plant.
  • Interact directly with customers during tech transfer, campaign preparation, execution, and closure, including daily reporting of batch status and performance.
  • Ensure timely compilation of process-related deviations, change requests, and campaign reports.
  • Compile CMC sections for filing documents and technical content for validation reports.

Key Requirements
  • PhD (preferred) or Master’s degree in biotechnology, chemical engineering, or related disciplines.
  • Significant working experience in biopharma manufacturing and/or process development, preferably in Mammalian Manufacturing.
  • Deep understanding of GMP and bioprocess technology.
  • Excellent communication skills and ability to interact with all kinds of interfaces within customers and the project organization.
  • Fluency in English is required; knowledge of German is a plus.

Practicalities
  • Location: Visp, Switzerland
  • Start-date: ASAP
  • Onsite
  • Duration: 1-year contract – with the likelihood of extension

Sound Interesting?
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her on +41 44 551 4407.

If you know someone who might be a good fit, feel free to introduce me to them. You can also refer a friend and earn €250,- for successful referrals.