About this role
Employee Responsibilities:
Provide analytical chemistry support to projects across the clinical drug development pipelineExecute test method protocols for in-vitro biopharmaceutics team that includes but not limited to thermodynamic solubility measurement, USP dissolution, precipitation and flux assaysPrepare analytical solutions and biorelevant media for in-vitro experiments, including accurate weighing, potency corrections, buffer preparation, and appropriate handling of active pharmaceutical ingredientsAnalyze study samples by HPLC and UV-vis, including calibration standard preparation, sample processing, and quantitation of drug concentration from in-vitro studiesPerform first-pass review of dissolution, solubility, and analytical data, identifying anomalous results (e.g., carryover, precipitation, coning, filtration loss) for scientific follow-upDocument findings in electronic lab notebooks and technical reports in accordance with ALCOA data integrity principlesSupport routine laboratory operations, including equipment readiness, consumables, safe lab practices, and scheduling instrumentsAdapt experimental execution and prioritization to shifting project needs, balancing scientific rigor with resource efficiency and study objectives The Ideal Candidate would possess:
Working knowledge of HPLC and UV-vis spectroscopy techniques, as they apply to quantitation of organic small molecules in solutionBasic proficiency in scientific data analysis like spreadsheet-based calculations and chromatography data interfacesExcellent oral and written communication, strong attention to detail, and strong quantitative abilityAbility to communicate and collaborate well in a cross functional environmentCustomer focused and comfortable supporting multiple project teams with shifting timelines, with a problem-solving mindset and a positive, optimistic attitudePreferred Qualifications include:
Hands-on experience executing in-vitro biopharmaceutics testing, such as USP dissolution, solubility, precipitation, or flux assaysProficiency in data analytic software like GraphPad Prism, Origin/Origin Pro, JMP etc.One to two years of wet lab experience in a pharmaceutical company or at a contracting organization.Minimum Qualifications:
Bachelor's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with 2+ years of relevant experience.
Master's degree in Chemistry, Pharmaceutics, Physical Chemistry, Biochemistry, or a related discipline with relevant experience.
Position is Monday- Friday 8:00 AM- 5:00PM. Overtime as needed. May be requested to work on weekends, overtime, and holidays based on business needsCandidates currently living within a commutable distance of Groton, CT are encouraged to apply.Excellent full-time benefits, including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysAuthorization to work in the United States indefinitely without restriction or sponsorshipEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.