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Manufacturing Suite Technical Manager (GMP) - California

Advanced Manufacturing Tech Solutions (AMTSOL)
Posted a month ago, valid for 15 days
Location

Vacaville, Solano 95687, CA

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • AMTSOL is seeking a MES PharmaSuite Technical Manager to join their team in Vacaville, California.
  • The ideal candidate should have a bachelor's degree in Engineering, Computer Science, or a related field, along with 10+ years of experience in MES implementations.
  • They must possess at least 7+ years of hands-on experience with PharmaSuite MES and a strong understanding of GMP pharmaceutical manufacturing processes.
  • The role involves managing complex integrations and ensuring compliance with quality standards and regulatory requirements.
  • Salary details are not specified, but the position requires significant experience in leading large-scale MES programs.

AMTSOL : A leader in Life Science Manufacturing Technology solutions, we are looking for top talent to be part of the dynamic team and drive the growth of the business.

Location: Vacaville, California, USA

MES PharmaSuite Technical Manager

Role Summary

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.

  • 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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