Validation Engineer
Kindeva Drug DeliveryLexington, Kentucky, United States
Posted January 7, 2026
Full Time
About the Company
Kindeva Drug Delivery is a purpose-driven Contract Development and Manufacturing Organization that specializes in advanced drug delivery platforms, including inhalation, microneedles, dermal, and injectable formulations. Leveraging a legacy of regulatory excellence and state-of-the-art facilities, the company partners with pharmaceutical developers to accelerate the transition of life-changing therapies from early-stage formulation to commercial production. Kindeva’s people-centric culture and focus on optimizing every step of the development cycle enable clients to achieve high-quality, compliant finished-dose products faster than traditional routes. The firm’s commitment to innovation, operational rigor, and strategic partnership positions it as a trusted ally for companies seeking to bring breakthrough medicines to market efficiently. Kindeva invites organizations to collaborate on shaping healthier tomorrows through its expertise in delivery technology and manufacturing excellence.
Job Description
As a Validation Engineer at Kindeva, you will play a key role in supporting the qualification and validation activities that ensure our manufacturing processes and equipment meet rigorous regulatory and quality standards.
Requirements
- Develop, execute, and review validation protocols for equipment, processes, and utilities in a GMP manufacturing environment.
- Support installation, operational, and performance qualification (IQ/OQ/PQ) activities to ensure equipment and systems meet design specifications.
- Collaborate with manufacturing, quality, engineering, and other stakeholders to ensure validation requirements are met.
- Participate in risk assessments and change control processes related to validation activities.
- Support continuous improvement initiatives for validation strategies and documentation.