Job Title: MES MBR Designer (PAS-X) -- Pharmaceutical Industry
Location: Ontario or Greater Toronto Area, Canada (or willing to relocate quickly)
Experience Required: Minimum 3 years in MES MBR Design
Contract Type: Full-time / Contract
Job Description
We 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 Responsibilities
- Design, develop, and test Master Batch Records (MBR) , Electronic Batch Records (EBR) , and global MBRs (gMBR) in PAS-X MES
- Collaborate with process engineers, QA, and production teams to capture business requirements and translate them into compliant MBRs
- Ensure 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 Requirements
- Minimum 3 years of experience as an MES MBR Designer
- Strong knowledge of PAS-X from Werum is mandatory
- Background in pharmaceutical or biotech manufacturing environments
- Experience designing and configuring MBRs/EBRs/gMBRs
- Understanding 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
