MES Automation Specialist (a)

Michael Page; Luzern; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Benefits dieser Stelle

Extension or takeover possibility

Zusammenfassung

Michael Page is recruiting an MES Automation Specialist for a 12-month, 100% onsite assignment near Lucerne, with extension option. The role focuses on configuring PAS-X GMBRs, performing changes, and ensuring validated MES operations in a biotech/pharma setting.

You will support SAP/DeltaV integrations, drive process improvements, and develop end-user training materials while adhering to SDLC and GAMP 5 guidelines.

Qualifikationen

• Degree in Life Sciences or equivalent with 2–3+ years in MES; PAS-X experience preferred.
• 2–4 years of Automation or Engineering experience in Biologics, Pharmaceuticals, Medical Devices, or Food industries.
• Knowledge of computer validation, SDLC, and change control practices (e.g., GAMP 5).
• Experience configuring, testing, and supporting MES GMBRs; PAS-X experience advantageous.
• Understanding MES integrations with automation systems (DeltaV) and SAP.
• Strong problem-solving and troubleshooting skills.
• Business fluent English.

Aufgaben

• Configuring, building, and maintaining PAS-X GMBRs and recipes per design standards and site requirements.
• Executing testing, verification, and documentation for GMBR releases and system changes.
• Supporting daily PAS-X operations, troubleshooting recipe execution and EBR issues.
• Supporting investigations and deviations by identifying and resolving MES/automation issues.
• Preparing and executing Change Controls, ensuring timely and compliant closure.
• Supporting MES administration and maintenance to maintain validated automation systems.
• Supporting PAS-X integrations with DeltaV, SAP, and related systems.
• Driving continuous improvement of business processes and MES workflows.
• Developing SOPs, training materials, and delivering MES end-user training.
• Ensuring SDLC-compliant documentation.
• Supporting MES-related Tech Transfer activities.
• Performing additional duties assigned by the MES Lead.

Kenntnisse

Automation experience

Engineering experience

Problem-solving

Troubleshooting

English proficiency

Ausbildung

Life Sciences degree

Tools

PAS-X

DeltaV

SAP

Kneat eVal

Jobbeschreibung

• 12 months contract with extension option

• International Biotech Company
• 12 months contract with extension option

About Our Client

For our client with modern offices in the Lucerne area, we are looking for a MES Automation Specialist (a) to join their team in October for the next 12 months. 100% onsite presence required.

Job Description

• Configuring, building, and maintaining PAS-X GMBRs and recipes per design standards and site requirements.
• Executing testing, verification, and documentation for GMBR releases and system changes.
• Supporting daily PAS-X operations, troubleshooting recipe execution and EBR issues.
• Supporting investigations and deviations by identifying and resolving MES/automation issues.
• Preparing and executing Change Controls, ensuring timely and compliant closure.
• Supporting MES administration and maintenance to maintain validated automation systems.
• Supporting PAS-X integrations with DeltaV, SAP, and related systems.
• Driving continuous improvement of business processes and MES workflows.
• Developing SOPs, training materials, and delivering MES end-user training.
• Ensuring SDLC-compliant documentation.
• Supporting MES-related Tech Transfer activities.
• Performing additional duties assigned by the MES Lead.

The Successful Applicant

• Degree in Life Sciences degree or equivalent experience, with 2-3+ years in MES; PAS-X experience preferred.
• 2-4 years of Automation or Engineering experience in Biologics, Pharmaceuticals, Medical Devices, or Food industries.
• Knowledge of computer validation, SDLC, and change control practices (e.g., GAMP 5).
• Experience with configuring, testing, and supporting MES GMBRs; PAS-X experience advantageous.
• Understanding MES integrations with automation systems (e.g., DeltaV) and SAP.
• Strong problem-solving and troubleshooting skills.
• Business fluent English.
• Experience with supporting commissioning, validation, and test protocol execution (e.g., Kneat eVal).

What's On Offer

Join a global biopharma leader, supporting state‑of‑the‑art digital manufacturing and MES. Collaborate within an international and cross‑functional team. Extension or take‑over possibility.

Contact

Quote job ref: JN-082026-7091540