Senior Analytical QA Lead; GMP & Method Validation
Listed on 2026-10-09
-
Quality Assurance - QA/QC
-
Healthcare
Lilly is seeking a Sr. Principal Associate for Analytical Quality Assurance in Indiana. The role ensures lab activities at the Lilly Medicine Foundry adhere to global and site quality standards and cGMP, maintaining data integrity and regulatory compliance.
The position supports design and construction phases, providing quality oversight for GMP testing, analytical development, and qualification of methods and instrumentation, while establishing and maintaining a robust quality management system.
We are looking to fill the Senior Analytical QA Lead (GMP & Method Validation) position at Regulatory Jobs in Lebanon, IN, United States.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Analytical QA Lead (GMP & Method Validation) role in the description above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).