DURATION - 6 MONTHS - ONSITE POSITION - SHIFT - MON - FRI 2PM - 10:30PM.

Job Description:

• 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, t...