Bioassay Data Review Specialist

Job Description Applies GMP/GLP in all areas of responsibility, as appropriate. Perform verification of data and confirm resolution of issues identified 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 Qualifications 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 to troubleshoot and problem‑solve in a cross‑functional setting Ability to read, comprehend, and present complex subjects Minimum Qualifications Bachelor's degree in biology, biochemistry, chemistry, or other related field, or equivalent directly‑related experience (two years of directly related industry experience equals one full‑time year of college in the related major) At least 3 years of related GMP pharmaceutical experience in an operations or testing role Authorization to work in the United States indefinitely without restriction or sponsorship Ensure adherence to highest quality and efficiency standards in laboratory operations Additional Information Position is full‑time, working Monday–Friday 8:00 a.m.–5:00 p.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 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. #J-18808-Ljbffr