Digitalization Consultant MES
In this role, you support the digitalisation of manufacturing processes within a regulated biopharmaceutical production environment. You contribute to MES (Manufacturing Execution System) projects aimed at converting paper batch records into electronic batch records across multiple manufacturing process steps.
You work closely with manufacturing, IT, and validation teams to translate complex production processes into functional MES solutions and ensure systems are validated and ready for operational use.
What will you do?
* Collect and document User Requirements (URS) for MES functionalities
* Translate biomanufacturing processes into functional MES requirements
* Test electronic batch records within the MES environment
* Support validation activities, including Performance Qualification (PQ)
* Collaborate with IT, validation teams, and production stakeholders
* Gradually take ownership of assigned MES process packages
* Support data integration activities when needed
Who are you?
* Bachelor’s or Master’s degree in Life Sciences, Engineering, IT, or related field
* Experience working in a regulated GxP environment
* Hands-on experience with MES systems
* Good understanding of validation lifecycle (URS, PQ, basic IQ/OQ)
* Strong communication and stakeholder management skills
* Ability to work autonomously after onboarding
* Fluent in English with good understanding of French
* Willingness to work mainly on-site in a manufacturing environment
Nice to have
* Experience in biopharmaceutical or pharmaceutical manufacturing
* Techno-functional or Business Analyst background
* Familiarity with OSIsoft PI or manufacturing data systems
* Experience working closely with production teams
What we offer
* A role at the intersection of manufacturing and digital transformation
* Involvement in MES implementation within a regulated production environment
* Collaboration with multidisciplinary teams across manufacturing and IT
* A competitive salary aligned with your experience and expertise