Position Overview
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...