Product Development Analytical Chemist
About The Position
Ability to work in a GLP or GMP environment with appropriate documentation and safety practices. Using routine laboratory techniques, support drug substance/drug product formulation development through hands-on generation of accurate and precise analytical chemistry data Techniques such as liquid chromatography (HPLC, UPLC), NMR (liquid), mass spectrometry, vibrational spectroscopy, gas chromatography, USP/EP dissolution testing, and/or Karl Fischer titration Development and execution of studies to ascertain degradation mechanisms in the solution and solid state. Development of assay/purity methods and assessment of method robustness/ruggedness Development and execution of method validation protocols. Development of dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure. Transfer of analytical methods to other laboratories and remote sites. Hands-on generation of data in support of accelerated and registration stability studies.
Requirements
- Ability to work in a GLP or GMP environment with appropriate documentation and safety practices.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Nice To Haves
- Candidates currently living within a commutable distance of Groton, CT, are encouraged to apply.
Responsibilities
- Support drug substance/drug product formulation development through hands-on generation of accurate and precise analytical chemistry data.
- Utilize techniques such as liquid chromatography (HPLC, UPLC), NMR (liquid), mass spectrometry, vibrational spectroscopy, gas chromatography, USP/EP dissolution testing, and/or Karl Fischer titration.
- Develop and execute studies to ascertain degradation mechanisms in the solution and solid state.
- Develop assay/purity methods and assess method robustness/ruggedness.
- Develop and execute method validation protocols.
- Develop dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure.
- Transfer analytical methods to other laboratories and remote sites.
- Generate data in support of accelerated and registration stability studies.
Benefits
- Comprehensive medical coverage
- Dental options
- Vision options
- Life insurance
- Disability insurance
- 401(k) with company match
- Paid vacation
- Paid holidays
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
