Kindeva Drug Delivery
The Quality Assurance In-Process (QAIP) Auditor I provides day-to-day support to manufacturing, packaging, and technical operations by conducting room and equipment line clearances, visual inspections, and in-process audits to ensure compliance with quality standards. The role involves real-time batch record reviews, sampling for stability and retain purposes, and performing daily facility walkthroughs to maintain audit readiness. This position requires enforcing cGMP regulations and collaborating with production teams to resolve quality issues and initiate investigations as needed.
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.
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