MES Automation Specialist (a)
Michael Page — Lucerne
Données OFS 2024 —
6'577 CHF / mois
Fourchette : 5'642 – 7'765 CHF (P25–P75), brut avant charges.
Comparez votre salaire → disponible avec Pro.
- 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
Your main tasks are as following:
- 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.
Quote job ref
JN-082026-7091540
Job Function
Engineering & Manufacturing
Specialisation
Test / Application / Commissioning
Industry
Healthcare / Pharmaceutical
Where
Lucerne
Contract Type
Interim
Job Reference
JN-082026-7091540
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