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Responsibilities include but are not limited to: Perform verification of data and confirm resolution of issues identified Perform 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 immediately Independently engage and collaborate with coworkers, customers, and management within a cGMP environment Must be able to identify problems and know when to solve proactively and seek advice Contribute and participate in investigations, as needed Support 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 environment Strong computer, scientific, and organizational skills Excellent written and oral communication with attention to detail Capability 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 needed Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply. 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 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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