BS / MS in Chemistry / Pharmaceutics with related science experience
2-4 years experience in pharmaceutical analytical chemistry is essential.
Hands-on experience with wet-chemistry and instrumental techniques (i.e., pH, titration, UV-Vis, GC, HPLC).
Experience in working within an FDA-regulated environment and GMP documentation requirements.
Previous experience with writing scientific protocols and reports.
Responsibilities :
Chemistry testing, data review and entry, protocol / report generation, laboratory maintenance and support.
Support and / or remediation to all chemistry-related projects for products currently on the market as well as participating in the conduct of the stability testing program to support the approval of process and / or product design changes.
Supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.