Verista, Inc.
The Senior Quality Engineer provides Quality Assurance oversight for GMP manufacturing operations of cell and gene therapy products, partners with cross‑functional teams to ensure compliance, and supports validation, qualification, and capital projects. The role also manages quality systems, investigations, and facility monitoring while fostering collaboration across Quality, Manufacturing, Engineering, and Validation groups.
Headquarters
Fishers, Indiana, United States
Company Size
501-1000 employees
Founded
2020
Verista is a life‑sciences consulting and engineering firm that supports pharmaceutical, biotech, medical device, and consumer‑health companies across the entire product lifecycle. They specialize in validation, quality and regulatory compliance, engineering and automation, commissioning/qualification, computer system validation, and digital transformation. Verista combines domain‑specific technical expertise and regulatory know‑how with hands‑on implementation to reduce risk, accelerate timelines, and ensure GxP compliance for complex manufacturing, clinical, and commercial operations.
Verista Announces New Partnership with Sware to Transform Digital Validation in the Life Sciences Industry
Aug 8, 2023
Verista Acquires Hawkins Point to Supercharge Business and Technology Prowess Across the Drug Development Lifecycle
Feb 2, 2021
The Top 25 Healthcare Technology Leaders of Dallas for 2023
Sep 25, 2023
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 Verista, Inc..
22% below the average for this role
Verista Announces the Appointments of New Chairman of the Board and Head of Growth & Business Development
Jul 19, 2023