Manager, Product Development GMP Operations

Job TitleManager, Product Development GMP OperationsLocationTampa, FL, USAThe actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.The Manager, Product Development GMP Operations is a site‑based leadership role supporting early‑phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic.What you will getAn agile career with opportunities for growth in a dynamic Product Development environmentA collaborative, inclusive, and ethical workplace cultureCompensation programs that recognize high performance and leadership impactCompetitive medical, dental, and vision insurance coverageAccess to Lonza’s learning, development, and leadership programsWhat you will do:Lead and develop Product Development GMP manufacturing and packaging operations supporting early‑phase clinical trial drug productsDesign, oversee, and maintain PD GMP spaces, including equipment selection, engineering build‑outs, and approval of engineering drawingsServe as the technical and operational SME for PD GMP activities, supporting projects, new technologies, and strategic growth initiativesProvide leadership and administrative management for a diverse technical team, including performance reviews, coaching, training, and career developmentEnsure compliance with cGMPs, SOPs, safety standards, and regulatory requirements, maintaining inspection readiness at all timesAct as a key internal and external stakeholder, participating in regulatory audits, client meetings, and on‑site visitsCoordinate closely with engineering, quality, manufacturing, and project teams to ensure timely, compliant, and cost‑effective delivery of workWhat we are looking for:Significant experience in early‑phase GMP drug product manufacturing and/or packaging within a pharmaceutical or life sciences environmentStrong understanding of cGMP regulations, quality systems, regulatory inspections, and audit readinessProven ability to lead technical teams, manage resources, resolve complex issues, and deliver results through othersExperience designing or supporting GMP facilities, including collaboration with engineering and oversight of build‑out activitiesEffective communication and stakeholder management skills, including customer‑facing and cross‑functional collaborationA scientific degree or similar field required, with an emphasis on applying knowledge to advance drug product developmentApproximately 15+ years of relevant experience with a bachelor’s or master’s degree, or 10+ years with a PhDAbout LonzaAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.SummaryLocation: US - Tampa, FLType: Full time