MSAT Consultant

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

Ready to drive cutting-edge sterile manufacturing processes and play a key role in bringing innovative biotech products to patients worldwide?

R&D Partners is seeking an MST Consultant to join a leading biotechnology company in Visp, Switzerland. This role focuses on supporting technical operations, including sterile drug product (DP) manufacturing processes, GMP validation, and MSAT standardization.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

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

Key Skills and Requirements:

• Strong expertise in sterile drug product manufacturing and GMP validation.
• Proven 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 skills within cross-functional teams.

For more information, please contact Jessica Taylor.