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Manufacturing Suite Technical Manager (GMP) - California at Advanced Manufacturing Tech Solutions (AMTSOL)

Vacaville, California, United States -

Full Time

Start Date

Immediate

Expiry Date

06 May, 26

Salary

0.0

Posted On

05 Feb, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

MES Implementation, PharmaSuite, GMP, Electronic Batch Records, System Configuration, Integrations, Testing, CSV, Regulated System Delivery, DeltaV DCS, Manufacturing, Quality, Automation, IT, Validation, Leadership

Industry

Pharmaceutical Manufacturing

Description

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

Responsibilities

The role involves leading the technical design, implementation, validation, and delivery of PharmaSuite MES solutions in GMP-regulated environments. The successful candidate will manage complex integrations and collaborate with various teams to ensure robust MES solutions.