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© All Rights Reserved. ApplyBlast.com
Kindeva Drug Delivery
A Process Validation Engineer at Kindeva supports the development, execution, and lifecycle management of process validation activities for pharmaceutical and sterile injectable products. The role involves authoring PPQ protocols, monitoring critical process parameters, supporting technology transfer, and ensuring compliance with cGMP and regulatory guidelines. Engineers collaborate cross-functionally with Manufacturing, Quality, and Regulatory Affairs to maintain robust and compliant manufacturing processes.
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.
22% below the average for this role