Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, Raw Material Testing, USP, EP, JP, Compendium Executing method transfer protocols Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Reads and understands analytical procedures (compendial and client supplied) and internal SOPs Processes data, generates reports, and evaluates data Writes investigations Leads project/test areas and perform method transfers/feasibility studies
Authorization to work in the United States indefinitely without restriction or sponsorship. Bachelor's degree in biology, 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) 2+ years of previous laboratory experience
The positions are full‑time and follow a 4x10 schedule. Available shifts include: First shift, Tuesday through Saturday from 8:00 a.m. to 6:00 p.m., OR Second shift, Monday through Thursday from 3:00 p.m. to 1:00 a.m. 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.