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Be ready to walk through how you mentor operators and peers on flow and quality, handle deviations and CAPAs, and balance coaching with compliance at a manufacturing site. Prepare examples of process improvements, training moments that stuck, and how you partner with production under regulated constraints.
Best fit for quality or manufacturing professionals who coach well on the floor, know regulated pharma QA practices, and want an on-site Foundry mentor/advisor role—not a remote desk job.
As Advisor, Flow Mentor, Manufacturing Quality Assurance at the Lilly Medicine Foundry site in Lebanon, Boone County, the day centers on coaching production and QA teams on process flow, right-first-time quality, and deviation prevention on the manufacturing floor. Expect Gemba-style mentoring, batch-record and procedure coaching, CAPA and investigation support, and partnering with operations to keep Foundry workflows compliant and capable. Much of the work is on-site mentoring rather than pure desk QA.
No. The listing is on-site in Lebanon, Boone County (remote flag is 0).
Coaching manufacturing quality and process flow at the Medicine Foundry—mentoring teams while protecting compliance and capability.
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Website: mairiedelilly.fr
Lilly is a commune in the Eure department in Normandy in northern France.
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Join Lilly's manufacturing team in Lebanon, Boone County, as an Advisor and Flow Mentor focused on Manufacturing Quality Assurance. This full-time position offers the chance to shape operational excellence at a leader in pharmaceutical innovation, where your expertise directly impacts the medicines that improve patient lives worldwide. The Opportunity Lilly's commitment to discovering and delivering life-changing medicines depends on unwavering quality and continuous improvement across our global manufacturing operations. In this advisory role, you'll guide your team through quality assurance processes, mentor colleagues in best practices, and drive operational enhancements that keep production running at peak efficiency. Your insights will help ensure that every medicine we produce meets the exacting standards patients deserve. Day-to-Day Responsibilities Oversee quality control and assurance activities across manufacturing processes Mentor team members on quality standards, compliance procedures, and continuous improvement methodologies Identify process inefficiencies and recommend data-driven solutions to optimize manufacturing workflows Ensure adherence to regulatory requirements and Good Manufacturing Practices (GMP) Document and communicate quality metrics, findings, and improvement initiatives Collaborate with cross-functional teams to troubleshoot issues and implement corrective actions Skills & Qualifications Proven experience in manufacturing quality assurance or related quality management roles Strong understanding of pharmaceutical manufacturing standards and regulations Demonstrated ability to mentor, coach, and develop team members Excellent analytical and problem-solving capabilities Proficiency in quality documentation and statistical analysis Clear communication and interpersonal skills High school diploma or equivalent; bachelor's degree in chemistry, engineering, or related field preferred Working at Lilly Lilly's global workforce of over 50,000 professionals is dedicated to one core focus: bringing breakthrough medicines to people who need them. We believe in investing in our team members, creating pathways for growth, and building environments where precision and innovation naturally flourish. At our Lebanon, Boone County site, you'll contribute to manufacturing that meets the highest standards—knowing your work directly influences patient health and wellbeing worldwide. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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