Analytical Development Reviewer — cGMP Data & Method Expert
Listed on 2026-10-06
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Research/Development
August Bioservices, a Nashville-based CDMO, seeks an Analytical Documentation Specialist to lead and review reports, methods, and validation activities across development and commercial programs. You will collaborate with scientists, manage lifecycle activities, and ensure compliance with ICH/FDA/EMA guidelines while driving data integrity and timely delivery.
Ideal candidates have a Master’s with 2+ years in pharma or a Bachelor’s with 3–5 years, strong writing, and proficiency in HPLC/LC-MS,
As a Analytical Development Reviewer — cGMP Data & Method Expert, you will play an important part at August Bioservices, LLC in Nashville, TN, United States.
The advertised compensation is 110..
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 Analytical Development Reviewer — cGMP Data & Method Expert role in the description above.
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