Description
The Associate Quality Compliance role supports Product Quality Teams by reviewing and verifying data and documents for late-stage and commercial pharmaceutical products. Responsibilities include executing transactions in GMP systems such as Veeva, LIMS, Spotfire, and SampleManager; validating data sources; managing compliance activities across teams and projects; and providing feedback to document authors. The role requires a bachelor’s or master’s degree and at least three years of pharmaceutical industry or directly related experience, along with GMP knowledge, attention to detail, communication skills, and familiarity with GMP applications.
