Job Title: MES MBR Designer (PAS-X) -- Pharmaceutical IndustryLocation: Ontario or Greater Toronto Area, Canada (or willing to relocate quickly)Experience Required: Minimum 3 years in MES MBR DesignContract Type: Full-time / ContractJob DescriptionWe are currently seeking a MES MBR Designer with hands-on experience in PAS-X to join our client in the pharmaceutical industry.
This is a great opportunity for someone passionate about digital manufacturing and electronic batch records to contribute to a growing, fast-paced environment in Ontario. Key ResponsibilitiesDesign, develop, and test Master Batch Records (MBR), Electronic Batch Records (EBR), and global MBRs (gMBR) in PAS-X MESCollaborate with process engineers, QA, and production teams to capture business requirements and translate them into compliant MBRsEnsure all MBRs align with GMP, 21 CFR Part 11, and company standards
Participate in validation activities, including system testing and documentation review
Support MES troubleshooting and contribute to continuous improvement initiatives
Work cross-functionally with IT and manufacturing teams to ensure efficient MES integration and deployment
Profile RequirementsMinimum 3 years of experience as an MES MBR DesignerStrong knowledge of PAS-X from Werum is mandatory
Background in pharmaceutical or biotech manufacturing environments
Experience designing and configuring MBRs/EBRs/gMBRsUnderstanding of GMP regulations, data integrity principles, and MES best practices
Strong problem-solving skills and ability to work independently or as part of a team
Based in Ontario, Greater Toronto Area or willing to relocate quickly
