Siemens Opcenter MES Consultant

RED GLOBAL TRANSPORTES; Lyon; Hybrid; EUR 129,000 - 203,000; Full time

Job summary

Siemens Opcenter MES Consultant is sought for a hybrid role in Lyon for a 12-month freelance contract starting January 2027. The project migrates from an existing MES to Siemens Opcenter in a pharmaceutical/GxP environment, with close collaboration across Smart Factory, Production, Quality and Automation teams.

French and English fluency required; responsibilities include configuring MES, adapting production specifications, IQ/OQ/PQ test activities, and supporting qualification and validation in

Qualifications

• Experience with Siemens Opcenter MES in pharmaceutical/GxP.
• Proven track record of MES configuration and implementation.
• Experience with MES migration projects, especially migrations to new MES environments.

Responsibilities

• Configure MES and set up production workflows, electronic recipes, and master data.
• Support migration from existing MES to Siemens Opcenter.
• Execute IQ/OQ/PQ testing and write qualification reports.

Skills

Siemens Opcenter MES

MES configuration

MES migration

Electronic recipes

Master data management

IQ/OQ/PQ

Pharmaceutical/GxP validation

Documentation & communication

French & English fluency

Job description

### SIEMENS OPCENTER MES Consultant - FreelanceLocation: Hybrid in Lyon, France Contract: 12 months, freelance Start: January 2027Languages: French & English### About the RoleWe 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 GxP 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 GxP 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/GxP 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/136939\\_1790006492