Description
Experience required:- 5 years working in a FDA regulated industry, specifically in a cGMP environment.
- 2 years experience working with Method Development and Method Validation.
- Comfortable reviewing QA documentation- CAPA, Deviations, Change Control, Test Methods, etc...
- Experience working cross-functionally between groups within a pharmaceutical organization.
- Analytical Lab Experience.
Skills Required:
- Strong communication skills
- Knowledge of FDA requirements and understanding of Regulatory Submissions
- Product Development
-
Overall understanding of GMP requirements for manufacturing -
Analytical thinker
- B.S. Degree- (Preferably) Chemistry
To find out more about Real please visit www.realstaffing.com