Full-time

Manager / Sr. Manager – Quality GMP

Posted by Monte Rosa Therapeutics • June 13, 2026

📍 basel, basel stadt, Switzerland
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Description

The Manager, GMP Quality is responsible for the oversight and day-to-day quality interface with CDMO producing DS & DP for MRTx's ongoing clinical programs.. This includes supporting the review of MBRs/EBRs, analytical methods, validation protocols/reports, specifications, release data packages and stability protocols/report. This role will also supportextneral audits , inspection readiness and regulatory authority inspections.

CDMO & Vendor Quality Oversight

  • Primary GMP/GDP Quality contact for identified vendors (DS & DP) supporting clinical programs; day-to-day quality interface.
  • Support new vendor qualification, audits and Quality Technical Agreements (QTAs) management.
  • Monitor vendor compliance; elevate risks to Sr. Leadership in a timely, structured manner.

Documentation & Quality Systems

  • Author and maintain GMP/GDP SOPs with a phase-appropriate approach; develop and provide cGMP and other GxP traini...

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