Job Description
What a great opportunity with a growing generic pharmaceutical company.
If you have the following, let me know!
- Minimum BS/MS in a Scientific field.
- Minimum 1-3 years’ experience in pharmaceuticals in R&D and 2-4 years’ in QC setting.
- R&D/QC experience in the Generic Pharmaceutical industry, however R&D experience would be preferable
- Experience handling controlled substances within DEA requirements is preferable.
- Knowledge in Good Documentation practices. Knowledge in USP/ICH/FDA/DEA regulations preferable.
Here is what you will do:
You will perform a variety of testing to assess the strength, identity and purity of finished product. You will work as a member of the Analytical R&D team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures.