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 functionalitiesTranslate biomanufacturing processes into functional MES requirementsTest electronic batch records within the MES environmentSupport validation activities, including Performance Qualification (PQ)Collaborate with IT, validation teams, and production stakeholdersGradually take ownership of assigned MES process packagesSupport data integration activities when needed
Who are you?Bachelor's or Master's degree in Life Sciences, Engineering, IT, or related fieldExperience working in a regulated GxP environmentHands-on experience with MES systemsGood understanding of validation lifecycle (URS, PQ, basic IQ/OQ)Strong communication and stakeholder management skillsAbility to work autonomously after onboardingFluent in English with good understanding of FrenchWillingness to work mainly on-site in a manufacturing environment
Nice to haveExperience in biopharmaceutical or pharmaceutical manufacturingTechno-functional or Business Analyst backgroundFamiliarity with OSIsoft PI or manufacturing data systemsExperience working closely with production teams
What we offerA role at the intersection of manufacturing and digital transformationInvolvement in MES implementation within a regulated production environmentCollaboration with multidisciplinary teams across manufacturing and ITA competitive salary aligned with your experience and expertise