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Siemens Opcenter MES Consultant

LYON, 69
il y a 1 jour

### SIEMENS OPCENTER MES Consultant - Freelance

Location: Hybrid in Lyon, France Contract: 12 months, freelance Start: January 2027Languages: French & English### About the Role

We are looking for an experienced **MES Consultant** to support a pharmaceutical manufacturing project involving the **migration from an existing MES solution to Siemens Opcenter**.

The consultant will be responsible for adapting existing production specifications, configuring the new MES, and supporting its implementation and qualification in line with site processes and Gx

P requirements.

The consultant will work closely with **Smart Factory, Production, Quality and Automation teams**, ensuring that the MES configuration is aligned with site production processes and compliant with applicable pharmaceutical and Gx

P requirements.### Key Responsibilities**MES Configuration & Setup**

  • Adapt existing MES specifications for the new MES environment.
  • Configure production workflows, including **electronic recipes and master data**.
  • Configure quality control points and associated alerts.
  • Configure equipment connected to the MES.
  • Support the migration from the existing MES environment to the new MES.**Testing & Qualification**
  • Perform dry runs.
  • Execute IQ activities in pre-production and production environments.
  • Write and execute **IQ/OQ/PQ** test protocols.
  • Perform test runs to resolve deviations and complete qualification activities.
  • Prepare qualification reports.### Required Experience
  • Strong hands-on experience with **Siemens Opcenter MES**.
  • Experience with **MES configuration and implementation**.
  • Experience with **MES migration projects**, particularly migration from an existing MES to a new MES environment.
  • Hands-on experience with production workflows, electronic recipes and master data.
  • Experience with MES qualification and validation in a **pharmaceutical/Gx

P environment**.

  • Good knowledge of **IQ/OQ/PQ** and pharmaceutical validation processes.
  • Experience working with Production, Quality, Automation and Smart Factory teams.
  • Ability to analyse existing MES specifications and adapt them to a new MES environment.
  • Strong documentation and communication skills.
  • Fluency in **French and English**.

If you think you are the right profile for this role, please apply with your CV.**Reference** CR/ \\_

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Entreprise
RED GLOBAL TRANSPORTES
Plateforme de publication
WHATJOBS
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