Manufacturing Suite Technical Manager (GMP) - California
About The Position
We are seeking an experienced MES PharmaSuite Technical Manager to lead the technical design, implementation, validation, and delivery of PharmaSuite MES solutions across GMP-regulated pharmaceutical manufacturing environments. This role will act as the technical authority for PharmaSuite programs, providing hands-on leadership and governance across the full MES lifecycle—from requirements and architecture through deployment, validation, and steady-state support. The successful candidate will drive end-to-end MES delivery, including Electronic Batch Records (EBR), system configuration, integrations, and testing, while ensuring strict alignment with business objectives, quality standards, and regulatory requirements. The role involves managing complex integrations with DeltaV DCS and other automation platforms, collaborating closely with Manufacturing, Quality, Automation, IT, and Validation teams, and ensuring robust, scalable MES solutions across single-site and multi-site programs.
Requirements
- Bachelor's degree in Engineering, Computer Science, or related field
- 10+ years of experience in MES implementations
- 7+ years of hands-on experience with PharmaSuite MES
- Proven experience leading large-scale or multi-site MES programs
- Strong understanding of GMP pharmaceutical manufacturing processes
- Strong understanding of Electronic Batch Records (EBR)
- Solid experience in CSV and regulated system delivery
- Experience integrating PharmaSuite with DeltaV DCS
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What This Job Offers
Job Type
Full-time
Career Level
Manager
