About this role
Responsibilities include but are not limited to:
Perform verification of data and confirm resolution of issues identifiedPerform cell culture, cell-based bioassay, and surrogate bioassays such as ligand-binding ELISA assays in plate-based formats in a GMP environment and other lab tasks for training and as needed.Anticipate 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 Bachelor’s degree in life science concentration (chemistry, biology, or related fields) and 2 to 4 years of directly related industry experience or a MS degree in a life science concentration (chemistry, biology, or related fields) and up to 2 years of directly related industry experience. 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 setting Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as neededCandidates currently living within a commutable distance of Indianapolis, IN 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 holidaysAuthorization to work in the United States indefinitely without restriction or sponsorshipEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.