Senior MES Engineer — PAS-X & Automation Integration Lead

Merck Gruppe - MSD Sharp & Dohme

Schachen

Vor Ort

CHF 120.000 - 170.000

Vollzeit

Vor 8 Tagen
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Zusammenfassung

Merck Gruppe - MSD Sharp & Dohme in Schachen, Switzerland, is seeking a Senior MES Engineer (m/f/d) to lead MES (PAS-X) solution implementation and support. You will coordinate recipes, ensure GMBR standards, and align MES with site automation for efficient biotech manufacturing.

The role requires hands-on PAS-X experience, strong SDLC and change-control knowledge, and demonstrated ability to drive continuous improvement across cross-functional teams in a GMP environment.

Qualifikationen

  • Bachelor's degree in Life Science or related field with at least 5 years MES experience.
  • Minimum 3 years in Automation/Engineering for pharma or related industries.
  • Strong knowledge of SDLC and change control (GAMP 5).
  • Hands-on PAS-X experience including Master Recipe Management and design/build of GMBR/MBR.
  • Ability to work cross-functionally and manage multiple priorities.

Aufgaben

  • Own and optimize MES (PAS-X) integration with site automation.
  • Develop and maintain MES GMBRs and batch records.
  • Support Tech Transfer and GMP operations readiness.
  • Lead change controls and ensure ALCOA+ data integrity.
  • Provide MES SME guidance during audits and inspections.

Kenntnisse

MES expertise
PAS-X experience
GMP knowledge
Cross-functional collaboration

Ausbildung

Bachelor’s degree in Life Science or related field

Tools

PAS-X
DeltaV
Kneat eVal
Weigh & Dispense

Jobbeschreibung

Merck Gruppe - MSD Sharp & Dohme in Schachen, Switzerland, is seeking a Senior MES Engineer (m/f/d) to lead MES (PAS-X) solution implementation and support. You will coordinate recipes, ensure GMBR standards, and align MES with site automation for efficient biotech manufacturing.

The role requires hands-on PAS-X experience, strong SDLC and change-control knowledge, and demonstrated ability to drive continuous improvement across cross-functional teams in a GMP environment.

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