MES Technical Lead — Lead GMP Manufacturing Excellence

Lonza Group Ltd.; Oberwallis; Sur place; CHF 110 000 - 150 000; Plein temps

Avantages offerts par ce poste

Agile career and dynamic work culture

Inclusive and ethical workplace

Compensation programs recognizing high

Résumé du poste

Lonza Group Ltd. seeks an MES Technical Lead for daily production tasks. You and the MES team report to the Team Lead Documentation and collaborate with stakeholders to optimize efficiency. You will train team members, support performance reviews and help develop their skills for future growth.

You will drive safety, GMP compliance and deviations handling while coordinating resources and participating in audits and improvement projects, ensuring a high‑quality manufacturing environment.

Qualifications

• Bachelor or Master in Pharmaceutical Technology, Chemistry, Pharmacy or related field.
• Experience with MES recipe authoring, preferably Emerson Syncade.
• Knowledge of DeltaV is an asset.
• Coordinate resources and workflows effectively.
• Previous lead experience for a technical team is an asset.
• Fluency in English; German is advantageous.

Responsabilités

• Set priorities and allocate resources to meet deadlines.
• Communicate with stakeholders across teams.
• Participate in improvement projects and audits.
• Ensure safety and GMP compliance on the shop floor.
• Identify and eliminate deviations in processes.
• Provide frontline MES technical support to manufacturing, QA and plant engineers.
• Train MES team members and support onboarding of new joiners.

Connaissances

MES recipe authoring

Emerson Syncade

DeltaV

team leadership

GMP safety

communication

Formation

Bachelor / Master Degree

Outils

Emerson Syncade

DeltaV

Description du poste

Lonza Group Ltd. seeks an MES Technical Lead for daily production tasks. You and the MES team report to the Team Lead Documentation and collaborate with stakeholders to optimize efficiency. You will train team members, support performance reviews and help develop their skills for future growth.

You will drive safety, GMP compliance and deviations handling while coordinating resources and participating in audits and improvement projects, ensuring a high‑quality manufacturing environment.