Qualifications
- 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.
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
- The position is full-time, Monday through Friday, 8am-5 pm
- May be requested to work on weekends, overtime, and holidays based on business needs.
- Candidates currently living within a commutable distance of Groton, CT , **** are encouraged to apply.
- Ability to work overtime as required.
- Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
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Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.