About this role
Perform various type of testing using chromatographic systems, HPLC, GC, ICExecute 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 staff -Minimum Required: Bachelors, Science discipline
-Chromatography Experience: BS: 4+ years; MS: 2 years
-Familiarity with United States Pharmacopeia testing requirements and techniques preferred
-Experience with HPLC and GC analysis, with ability to maintain and troubleshoot instruments
-Ability to author reports/investigations and execute protocols with limited support
-Capable of generating scientifically valid data in accordance with GMP practices
-Ability to work autonomously on projects after training is completed is essential
Position is full-time, Monday - Friday 8:30am - 5pm. Candidates currently living within a commutable distance of Jacksonville, FL 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 holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.