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MES Automation Specialist (a)

Lucerne Interim View Job Description
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.

Added 27/08/2026

  • 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 summary

Job Function
Engineering & Manufacturing
Specialisation
Test / Application / Commissioning
Industry
Healthcare / Pharmaceutical
Where
Lucerne
Contract Type
Interim
Job Reference
JN-082026-7091540

Michael Page is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.