MSAT Lead: Sterile DP Manufacturing & Validation

R Dpartners

Zermatt

Vor Ort

CHF 120.000 - 180.000

Vollzeit

Vor 13 Tagen
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Zusammenfassung

R&D Partners is seeking an MST Consultant to join a leading biotechnology company in Visp, Switzerland. You will support sterile drug product manufacturing, GMP validation, and MSAT standardization to drive consistent operations.

You will lead cross-functional teams through process transfer, scale-up, and deviation investigations, ensuring compliant, data-driven decisions and timely delivery of competitive therapies to patients.

Qualifikationen

  • Strong expertise in sterile drug product manufacturing and GMP validation.
  • Experience in MSAT workflows and operational standardization.
  • Ability to manage complex deviations and lead data-driven investigations.
  • Familiarity with technology assessments and scale-up processes for aseptic manufacturing.
  • Excellent communication and collaboration with cross-functional teams.

Aufgaben

  • Lead the implementation, transfer, and optimization of sterile DP manufacturing processes with cross-functional project teams.
  • Deliver compliant product and process qualification activities aligned with regulatory and customer expectations.
  • Develop and embed harmonized MSAT workflows to enhance operational consistency for sterile DP manufacturing.
  • Resolve technical challenges through data-driven investigations, impact assessments, and structured quality actions.
  • Drive technology assessments, scale-up activities, and engineering readiness for aseptic drug product manufacturing.

Kenntnisse

Sterile DP manufacturing
GMP validation
MSAT workflows
Data-driven investigations
Scale-up processes
Cross-functional collaboration

Jobbeschreibung

R&D Partners is seeking an MST Consultant to join a leading biotechnology company in Visp, Switzerland. You will support sterile drug product manufacturing, GMP validation, and MSAT standardization to drive consistent operations.

You will lead cross-functional teams through process transfer, scale-up, and deviation investigations, ensuring compliant, data-driven decisions and timely delivery of competitive therapies to patients.

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