Ability to work in a GLP or GMP environment with appropriate documentation and safety practices.
Experience with GMP, wet chemistry, HPLC, Raman, FTIR are required
Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post-packaging support.
Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV), and compound-specific methods.
Set up and analysis of drug substance and drug product stability samples.
Method development and validation of analytical methods for drug substance and drug product
Hunt on autopilot
New GMP Analytical Chemist jobs in Groton, in your inbox.
The boar re-runs this search every day and emails you what’s new — scraped straight from company career sites, no recruiter spam. Free.