MES Techno-Functional Consultant
MSI Pharma, Sauk Trail Beach, WI, United States
Techno Functional Consultant MES – Freelance | Belgium near Brussels
Contract:
Initial twelve months with strong possibility of extension
Mission We are supporting a Belgian Biopharmaceutical company with two MES techno/functional consultant hires. They are looking for two consultants to support the digitalisation of biomanufacturing processes by helping convert paper batch records into fully electronic batch records across upstream, downstream and buffer preparation steps.
What you will do
Collect and write User Requirements URS for MES
Translate biomanufacturing process steps into clear functional requirements
Test electronic batch records within the MES environment
Carry out Performance Qualification PQ activities
Work closely with IT and validation teams
Gradually take full ownership of assigned MES work packages
Occasionally collaborate with OSIsoft PI teams for data integration needs
Must have
Experience in regulated or GxP environments
Understanding of validation lifecycle including URS PQ and basic IQ and OQ
Hands on MES experience
Strong communication and stakeholder management
Able to work independently after onboarding
English required and French at least at understanding level
Comfortable being mostly on site
Nice to have
Background in biomanufacturing or pharmaceutical production
Knowledge of OSIsoft PI
Techno functional or Business Analyst type profile
Experience working close to production teams
Work setup
Location is Braine l'Alleud in Belgium
Mostly on site with up to two days remote per week
Candidates must already be based in Belgium
Please only apply if you have hands‑on experience in pharmaceutical or biomanufacturing environments, working on MES within regulated manufacturing settings. #J-18808-Ljbffr
Mission We are supporting a Belgian Biopharmaceutical company with two MES techno/functional consultant hires. They are looking for two consultants to support the digitalisation of biomanufacturing processes by helping convert paper batch records into fully electronic batch records across upstream, downstream and buffer preparation steps.
What you will do
Collect and write User Requirements URS for MES
Translate biomanufacturing process steps into clear functional requirements
Test electronic batch records within the MES environment
Carry out Performance Qualification PQ activities
Work closely with IT and validation teams
Gradually take full ownership of assigned MES work packages
Occasionally collaborate with OSIsoft PI teams for data integration needs
Must have
Experience in regulated or GxP environments
Understanding of validation lifecycle including URS PQ and basic IQ and OQ
Hands on MES experience
Strong communication and stakeholder management
Able to work independently after onboarding
English required and French at least at understanding level
Comfortable being mostly on site
Nice to have
Background in biomanufacturing or pharmaceutical production
Knowledge of OSIsoft PI
Techno functional or Business Analyst type profile
Experience working close to production teams
Work setup
Location is Braine l'Alleud in Belgium
Mostly on site with up to two days remote per week
Candidates must already be based in Belgium
Please only apply if you have hands‑on experience in pharmaceutical or biomanufacturing environments, working on MES within regulated manufacturing settings. #J-18808-Ljbffr