Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus Execute specialized analyses and method transfer and feasibility testing Document work as required for GMP compliance Perform tests accurately Troubleshoot method and instrumentation problems Use office and instrumentation specific computer software Produce written reports (e.g., SOP, OMC, client reports) Develop and execute validation plans Carry out method transfers and feasibility studies Train technical staff Some travel to client sites for technical meetings could be required
Minimum Qualifications: Bachelor's or Master's degree in chemistry or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Three years related pharmaceutical experience in a cGMP environment Authorization to work in the United States indefinitely without restriction or sponsorship 4-8 years of experience within the industry Experience using EMPOWER and HPLC Experience with validation
Working schedule will be Full-Time, First Shift, Monday-Friday 8am-4m. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. 25% travel may be required. This position is NOT remote. What we Offer: 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 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.