About this role
Applies GMP/GLP in all areas of responsibility, as appropriate.
Perform verification of data and confirm resolution of issues identifiedAnticipate quality events or issues and elevate them to appropriate management attention immediatelyIndependently engage and collaborate with coworkers, customers, and management within a cGMP environmentMust be able to identify problems and know when to solve proactively and seek adviceContribute and participate in investigations, as neededSupport regulatory and client inspections, as needed Proficiency in cGMP and FDA-regulated clinical services laboratory environmentStrong computer, scientific, and organizational skillsExcellent written and oral communication with attention to detailCapability to work well on a team and be able to troubleshoot and problem-solve in cross-functional team settingAbility to read, comprehend, and present complex subjectsMinimum Qualifications:
Bachelor's degree in biology, biochemistry, 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)At least 3 years of related GMP pharmaceutical experience in either an operations or testing roleAuthorization to work in the United States indefinitely without restriction or sponsorshipEnsure adherence to highest quality and efficiency standards in laboratory operationsAuthorization to work in the United States indefinitely without restriction or sponsorship Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as neededExcellent full-time benefits, including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.