Kindeva Drug Delivery
A Quality Assurance role at Kindeva focusing on GMP compliance, documentation review, and manufacturing support in a pharmaceutical environment. The role involves coaching colleagues, conducting audits, and supporting continuous improvement initiatives within aseptic processing areas.
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.
40% below the average for this role
Qualified Person (QA)
GE HealthCare
QA Investigations Coordinator
Viatris
Operational Coordinator (Mon-Thurs Night Shift)
AstraZeneca
Packaging Shift Coordinator
State of North Carolina
Manufacturing Quality Assurance Specialist, 3rd shift (Monday-Friday, 11 PM-7:30 AM)
AbbVie
Assistant Manager Production
GSK plc