Supervisor, GMP and Technical Training

Supervisor, GMP and Technical TrainingHouston, TXThe actual location of this job is in Houston, TX, US. Relocation assistance is available for eligible candidates and their families, if needed.This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.What you will get: An agile career and dynamic working culture.An inclusive and ethical workplace.Compensation programs that recognize high performance.A variety of benefits dependent on role and location.The full list of our global benefits can be found here: .What you will do:Design, develop, and deliver instructor-led, hands-on, and on-the-jobtraining programs for manufacturing personnel.Qualify and certify manufacturing employees on production processes,aseptic techniques, cleanroom behaviors, equipment operation, and GMPdocumentation practices.Maintain training curricula, qualification matrices, and training records inaccordance with regulatory requirements.Partner with Manufacturing leadership to identify skill gaps and developtargeted training plans.Conduct training effectiveness assessments and implement continuousimprovements to training programs.Support onboarding of new manufacturing employees through structuredlearning pathways.Collaborate with Subject Matter Experts (SMEs) to develop and revisetraining materials, job aids, and standard work documentation.Support deviation investigations related to training deficiencies andimplement corrective actions when required.Assist with new product introduction (NPI) activities by developing anddelivering training associated with new processes, equipment, andprocedures.Participate in internal audits, regulatory inspections, and customer auditsas a training subject matter expert.Monitor training compliance and proactively address overduequalifications.Support both day shift and night shift based on business needsPerform other duties as assigned.What we are looking for:Bachelor's Degree in Life Sciences, Biotechnology, or related field5-10 Years of experience if biotech/biopharma laboratory or manufacturing experience preferably in a Cell Therapy manufacturing environment. Excellent communication skills (oral and written)Excellent Aseptic Technique and Cleanroom SkillsAbility to perform aseptic gowning on a daily basisComputer software skills (i.e. Cornerstone, Microsoft Office, Trackwise)Database and spreadsheet creation and maintenanceOrganization, record keeping, and planning skillsManaging multiple projects, time management skillsPeople management and training methodsAble to assess and recommend training needs and training assignments/requirements/curricula.Ability to lead cross-functional consultation on training strategy, strong facilitation and delivery skills, and ability to coordinate complex training initiatives.Skilled in coaching, training, and facilitation practicesAbility to travel at least 20% travel based on site location and or client visitsAbout 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 value diversity and are committed to creating an inclusive environment for all employees. 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 - Houston, TXType: Full time