Job Description

Job Description Responsible for utilizing analytical methodologies, systems , and processes to support drug substance and drug product development throughout all phases. Prepare, set up, and analyze drug substances and/or drug product samples using a variety of analytical techniques including chromatography (e.g., HPLC, UPLC, LCMS GC, GCMS, SFC), spectroscopy (e.g., UV-Vis, NMR), dissolution, and other relevant methodologies (e.g., KF, pH, ROI). Support development and optimization of analytical methods, including assay, purity, dissolution, and/or impurity characterization approaches as appropriate. Execute method qualification, validation, and transfer activities to support development and commercialization programs. Conduct degradation, stability, and investigational studies to support the evaluation of product performance and risk. Assess stability, dissolution, and/or impurity trends to support product and process development decisions. Support analytical method and technology transfer activities across laboratories and development sites. Operate, maintain, calibrate, and troubleshoot analytical instrumentation under guidance. Read and understand analytical methods, SOPs, compendial procedures, and GMP requirements while maintaining accurate documentation and data integrity within electronic laboratory systems. Demonstrate strong ownership of quality, safety, productivity, organization, and client service expectations. Perform other duties as assigned Qualifications Bachelor’s degree in chemistry, biochemistry, or other related degree concentration, or equivalent directly-related experience Basic laboratory skills and following written procedures, protocols, and work instructions accurately Strong computer, scientific, and organizational skills Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Experience in GMP laboratory, analytical chemistry Experience with eLN and data trending Additional Information Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. 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 \ #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. Compensation: $22-$22 #J-18808-Ljbffr

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