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Mes consultant – siemens opcenter execution pharma (ebr)

CDI
Cognizant
Publiée le 7 février
Description de l'offre

About the role

As a MES Consultant – Siemens Opcenter Execution Pharma (eBR), you will make an impact by transforming manufacturing processes within regulated pharma environments through the design, configuration, and validation of electronic Batch Records (eBR). You will be a valued member of our Life Sciences Manufacturing Systems team and collaborate closely with business SMEs, MES engineering teams, Cognizant leadership, and customer stakeholders to deliver high‑quality MES solutions.


In this role, you will

* Assess manufacturing requirements and translate them into functional MES designs.
* Collaborate with Business SMEs / Key Users to understand, refine, and document process needs.
* Work with MES engineers to design, configure, validate, and test Siemens Opcenter Execution Pharma PIs.
* Identify cross‑site commonalities and drive the creation of global reusable PIs.
* Produce required documentation including URS, FRS, design specifications, and test scripts.
* Lead and mentor team members, assigning work and ensuring delivery quality.
* Provide regular progress updates to Cognizant management and customer leadership.


Work model

We believe hybrid work is the way forward. Based on this role’s business requirements, this is a hybrid position requiring regular presence in Brussels, Belgium.


What you need to have to be considered

* Strong understanding of pharmaceutical manufacturing processes.
* Experience with Siemens Opcenter Execution Pharma / Simatic IT eBR.
* Extensive experience designing PIs based on site‑specific requirements.
* Ability to identify common processes across sites and build global, scalable PIs.
* Strong background in validating PIs and supporting MES testing activities.
* Good documentation skills (URS, FRS, design specs, test scripts).
* Ability to collaborate with both business and technical stakeholders.


These will help you stand out

* Experience working in GMP‑regulated environments.
* Knowledge of MES architecture and integration in pharma manufacturing.
* Hands‑on experience leading teams in MES delivery projects.
* Understanding of global template design and multi‑site deployment models.


What we offer:

* Health insurance
* Life cover
* Car or mobility budget
* Work-from-home allowance
* 32 vacation days
* Pension plan
* Luncheon vouchers
* Travel insurance
* EcoCheques
* Travel & entertainment cost reimbursement
* Laptop
* Mobile phone with subscription
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