MSAT Lead: Sterile DP, GMP & Standardization Expert

R&D Partners; Oberwallis; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Zusammenfassung

R&D Partners in Visp, Switzerland is seeking an MST Consultant to advance sterile drug product manufacturing, GMP validation, and MSAT standardization within a leading biotech setting.

This role involves leading cross-functional teams, conducting data-driven investigations, overseeing scale-up activities, and ensuring engineering readiness for aseptic DP production. Applicants must have the right to work in Switzerland.

Qualifikationen

• Experience in sterile DP manufacturing and GMP validation.
• Proven track record with MSAT workflows and standardization.
• Ability to manage complex deviations and investigations.
• Familiarity with technology assessments and aseptic scale-up.
• Excellent communication and cross-functional collaboration.

Aufgaben

• Lead sterile DP process implementation, transfer and optimization with cross-functional teams.
• Deliver GMP validation activities aligned with regulatory expectations.
• Develop and embed MSAT workflows for operational consistency.
• Resolve complex deviations through data-driven investigations.
• Drive scale-up activities and engineering readiness for aseptic DP manufacturing.

Kenntnisse

Sterile DP manufacturing

GMP validation

MSAT workflows

Data-driven investigations

Cross-functional collaboration

Jobbeschreibung

R&D Partners in Visp, Switzerland is seeking an MST Consultant to advance sterile drug product manufacturing, GMP validation, and MSAT standardization within a leading biotech setting.

This role involves leading cross-functional teams, conducting data-driven investigations, overseeing scale-up activities, and ensuring engineering readiness for aseptic DP production. Applicants must have the right to work in Switzerland.