Verista, Inc.
Verista is seeking an experienced Senior Process Engineer to support GMP biologics drug substance manufacturing within a CDMO environment. The role focuses on technology transfer, process scale-up, manufacturing support, and technical troubleshooting to help clients improve lives. The ideal candidate will provide technical expertise in upstream and/or downstream biologics operations while ensuring successful process execution and quality compliance.
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,
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Verista Announces the Appointments of New Chairman of the Board and Head of Growth & Business Development
Jul 19, 2023
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