About this role
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 apparatusExecute specialized analyses and method transfer and feasibility testingDocument work as required for GMP compliancePerform tests accuratelyTroubleshoot method and instrumentation problemsUse office and instrumentation specific computer softwareProduce written reports (e.g., SOP, OMC, client reports)Develop and execute validation plansCarry out method transfers and feasibility studiesTrain technical staffSome travel to client sites for technical meetings could be required The Ideal Candidate would possess:
1-2 years of transferable laboratory experienceExperience using EMPOWER and HPLC in industryExperience with validation in industryMinimum 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)3 years related pharmaceutical experience in a cGMP environmentAuthorization to work in the United States indefinitely without restriction or sponsorship Working schedule will be Full-Time, First Shift, Monday-Friday 8am-4pm. 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 optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.