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.

Required:

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.