MES MBR Design Engineer - GMP-Driven Pharma Tech

Incyte; Yverdon-les-Bains; Vor Ort; CHF 90.000 - 120.000; Vollzeit

Zusammenfassung

Incyte is seeking an experienced Engineer MBR Design to ensure configuration and parametrization of the MES system (MBR) in a GMP-compliant biopharmaceutical manufacturing environment. You will design manufacturing processes in MES, support engineering activities, and contribute to MES improvement projects across interfaces such as SAP, LIMS, and PCS.

The role requires a minimum of 5 years as an MBR creator/MES Admin in pharma, with strong GMP knowledge and fluency in English and French.

Qualifikationen

• Bachelor’s degree or equivalent in a relevant field (pharmacy/biotech/chemistry).
• Minimum 5 years as an MBR creator/MES Admin in biopharma manufacturing.
• Proven GMP knowledge and regulatory experience.
• Fluent in English and French; strong written/verbal communication.

Aufgaben

• Realize MES MBR and update master data per manufacturing planning.
• Drive MBR release planning to deliver required MBR on time.
• Review and technically approve MBR with cross-functional teams.
• Create/change controls, deviations, investigations, and CAPAs related to MBR.
• Train MES users and participate in MES on-call and audits.

Kenntnisse

GMP knowledge

Biopharma experience

English proficiency

French proficiency

Problem solving

Quality mindset

Ausbildung

Bachelor’s degree in pharmacy/biotech/chemistry

Equivalent pharmaceutical industry experience

Tools

PAS-X MES

MES admin

Jobbeschreibung

Incyte is seeking an experienced Engineer MBR Design to ensure configuration and parametrization of the MES system (MBR) in a GMP-compliant biopharmaceutical manufacturing environment. You will design manufacturing processes in MES, support engineering activities, and contribute to MES improvement projects across interfaces such as SAP, LIMS, and PCS.

The role requires a minimum of 5 years as an MBR creator/MES Admin in pharma, with strong GMP knowledge and fluency in English and French.