Senior MES Support Engineer L3
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Experience:
5-10 years /liliDepartment: Engineering functions /liliTypes of work contract: Permanent /li /ulh3Company Description /h3pEverience is an international consulting group delivering AI-augmented digital services and placing people at the heart of the AI revolution. /ppWith a presence in Europe, Africa, Asia and America, Everience offers its 4,000-strong workforce the most demanding and stimulating environment in which to transform and develop their skills, learning about new AI-based roles and building their future employability. /ppThrough its Symbiotic Academy the group offers a unique hub for training, practical application and exchange where everyone can experiment, learn, and progress in the fields of artificial intelligence and data. /ppIn accordance with its core purpose of orchestrating the symbiotic relationship between humans and AI in the workplace, Everience is making the augmented employee the driving force of a “symbiotic age”, where AI enhances talents and opens up new career opportunities. /ph3Job Description /h3ulliAct as the primary escalation point for complex MES incidents and production issues. /liliConfigure, administer, and optimize MES functionalities supporting GMP manufacturing activities. /liliPerform root cause analysis and implement permanent corrective actions. /liliSupport electronic batch records, manufacturing workflows, and production processes. /liliLead technical changes, deployments, and system enhancements. /liliCollaborate with Quality Assurance, Validation, Manufacturing, Engineering, and IT teams. /liliEnsure compliance with GMP, GxP, Computer System Validation (CSV), and Data Integrity requirements. /liliSupport audits and regulatory inspections. /liliMentor L1/L2 support teams and provide expert guidance. /liliParticipate in global MES improvement and digital manufacturing initiatives. /li /ulh3Qualifications /h3ulliStrong experience supporting and configuring Manufacturing Execution Systems. /liliProven experience in L3 Application Support, MES Engineering, or Manufacturing Systems. /liliSolid understanding of GMP-regulated manufacturing processes. /liliExperience with validation documentation (IQ/OQ/PQ) and CSV methodologies. /liliKnowledge of batch record management and manufacturing execution processes. /liliStrong troubleshooting and analytical skills. /liliExperience with SQL, interfaces, and application integrations. /liliAbility to engage with both technical and business stakeholders. /li /ulh3Nice to Have: /h3ulliExperience with Werum PAS-X (highly preferred). /liliKnowledge of SAP-MES integrations. /liliFamiliarity with serialization and track trace processes. /liliExperience supporting biologics, vaccines, or pharmaceutical manufacturing sites. /liliExperience participating in regulatory audits and inspections. /li /ulh3Additional Information /h3pAll our positions are open to both women and men and are, of course, open to people with disabilities. /p
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