A QA Associate must be familiar with applicable GMP regulations and systems and have the ability to make independent decisions based those requirements.
This individual will be responsible for evaluating the compliance of analytical documentation such as test methods, protocols, and stability and release data with minimal supervision.
This individual must demonstrate excellent critical thinking and organizational skills.
Professional, effective, and proactive communication with peers, management, and interdepartmental colleagues is required.
Essential Duties and Responsibilities include the following.
Other duties may be assigned.
Review of analytical release and stability data, with minimal supervision.
Review and approval of controlled documents such as protocols, test methods, and specifications.