Kindeva Drug Delivery
Kindeva is seeking a seasoned Quality Assurance Validation Subject Matter Expert to lead the QA validation function at its sterile injectable GMP manufacturing site in Maryland Heights, MO. This role provides expert guidance and oversight for equipment qualification, process validation, computer system validation, and data integrity compliance to ensure regulatory alignment and operational efficiency. The position involves serving as the functional lead for validation, reviewing critical documentation, and acting as a subject matter expert during internal and external regulatory inspections.
Headquarters
Woodbury, Minnesota, United States
Company Size
1001-5000 employees
Founded
2020
Kindeva is a drug-delivery focused CDMO that specializes in developing and manufacturing drug–device combination products. They provide end-to-end services—from formulation and device design through clinical and commercial-scale manufacturing—supporting pharmaceutical and biotech customers with technical, quality, and regulatory expertise. Purpose‑fueled and people‑centric, Kindeva emphasizes collaborative partnerships and practical experience to advance clients’ projects and bring complex delivery solutions to market.
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 Kindeva Drug Delivery.
Kindeva Drug Delivery didn’t post a salary, so this is our estimate from similar listings.
7% below the average for this role
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