GMP Documentation & Audit Readiness Specialist
Listed on 2026-10-06
-
Pharmaceutical
Pharmaceutical Manufacturing
Medivant Healthcare in Chandler, AZ, is seeking a Manufacturing Documentation Associate (Lighthouse) to support environmental monitoring and documentation throughout the manufacturing process. You will ensure GMP compliance, maintain batch records, and coordinate documentation for packaging operations.
The role requires a Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or related field and 1–3 years of experience in pharmaceutical documentation or manufacturing.
We have an opening for a GMP Documentation & Audit Readiness Specialist in Chandler, AZ, United States within Engineering.
The position is based in Chandler, AZ, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 41.000 - 50.000.
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 GMP Documentation & Audit Readiness Specialist 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).