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© All Rights Reserved. ApplyBlast.com
VTI Life Sciences
A Senior Validation Lead oversees end-to-end validation lifecycle activities for GMP manufacturing equipment, facility utilities, and computerized systems in a regulated life sciences environment. This role involves authoring compliance documentation, coordinating cross-functional teams, and ensuring adherence to FDA, cGMP, and data integrity standards. The position requires technical expertise in both commissioning/qualification/validation (CQV) and Computer System Validation (CSV) across diverse pharmaceutical assets.
Headquarters
San Diego, California, United States
Company Size
51-200 employees
Founded
1996
VTI Life Sciences is a full-service cGMP Commissioning, Qualification, and Validation (CQV) services organization that has successfully managed and executed hundreds of validation projects for pharmaceutical, biotechnology, and medical device manufacturers. The company offers a comprehensive range of services including process validation, cleaning validation, computerized systems, automation services, regulatory affairs, quality assurance, and FDA 483 response and compliance services. VTI Life Sciences has been NQA ISO 9001-2015 certified since 1998 and serves regulated industries including biologics, cosmetics, consumer healthcare, and herbal medicine.
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
View leadership team, funding history,
and employee contacts for VTI Life Sciences.
VTI Life Sciences didn’t post a salary, so this is our estimate from similar listings.
Right around the average for this role