Employee Responsibilities:Perform method development, feasibility, qualification and/or validation of methods in support of large molecule biopharmaceutical productsDocument work as required for GMP compliancePerform tests accuratelyTroubleshoot method and instrumentation problemsUse office and instrumentation specific computer softwareProduce documents (e.g., characterization reports, methods and client reports)Develop and execute validation plansGive presentations for training and client reviewsTrain technical staff
