MMR Consulting
A Sr. CQV Manager/PM leads commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives across GMP-regulated facilities. The role involves overseeing cross-functional execution for equipment, utilities, and automation systems while ensuring compliance with FDA and cGMP standards. Candidates will manage large-scale projects, lead teams of engineers, and act as a key liaison between engineering, quality, and external vendors.
Headquarters
Carlsbad, California, United States
Company Size
51-200 employees
Founded
2017
MMR Consulting is a life sciences consulting firm providing end-to-end services in Commissioning, Qualification, and Validation (CQV), Computer System Validation (CSV), automation, project management, engineering, and GMP compliance. The company serves global pharmaceutical, biotech, and regulated industry clients, offering both technical staff augmentation and full project delivery. MMR Consulting is ISO 9001 certified and is a strategic partner for Kneat Paperless Validation software.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
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