Material Management Systems Improvement Specialist

Material Management Systems Improvement SpecialistAt Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.Achieve, Cooperate, Care and Innovate are the values ​​that we share and practice on a daily basis.Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.For more information on Guerbet, go to and follow Guerbet on Linkedin, Twitter, Instagram and YoutubeWHAT WE ARE LOOKING FORThe Material Management System Improvement Specialist will be operating in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.This role focuses on strengthening and improving the materials management lifecycle by translating regulatory requirements, system assessments, and operational insights into practical, sustainable enhancements. Working cross-functionally with Supply Chain, Quality, and Production, the Specialist helps ensure supplier oversight, material handling, and inventory controls meet GMP and regulatory standards while improving efficiency and reliability. It is a hands-on position dedicated to implementing improvements and driving consistent, compliant material management practices. THIS IS A CONTRACT ROLE THAT WILL LAST 18-24 MONTHS AND WILL BE ELIGIBLE FOR GUERBET BENEFITS.YOUR ROLELead and actively implement CAPAs and improvements originating from system assessments or internal reviews.Translate supplier, warehouse, and material management requirements into practical operational actions.Work with cross-functional teams to ensure corrective and preventive actions are fully embedded in processes and daily operations.Monitor progress, address operational barriers, and support resolution with relevant stakeholders.Verify effectiveness through structured follow-up, data trending, and operational observations.Strengthen supplier qualification, auditing, and monitoring programs, including corrective actions.Improve material approval, sampling, testing, release, and rejection processes aligned with compendial and GMP standards.Enhance material traceability, identification, and inventory control systems.Support warehouse operations to ensure proper segregation, inventory accuracy, and prevention of mix-ups.Partner with Production, Quality, and Supply Chain to ensure materials consistently meet GMP and regulatory requirements.Performs other duties as assigned by managementYOUR BACKGROUNDRequired QualificationsBachelor’s degree in Supply Chain, Life Sciences, Engineering, or a related field (or equivalent combination of education and experience).10+ years in Materials Management, Supply Chain, or Quality within GMP-regulated environments.Hands-on experience in supplier qualification, auditing, and material lifecycle management.Knowledge of GMP regulations, microbiology, endotoxin control, and global pharmacopeial requirements.Familiarity with electronic inventory systems, data integrity, and GMP-compliant warehouse operations.Strong cross-functional collaboration and project management skills.Preferred QualificationsAdvanced degree or certification in Supply Chain, Quality, or related discipline.Experience supporting regulatory inspections, audit readiness, or supplier quality programs.Experience in sterile or highly regulated manufacturing environments.Reason to join USMuch more than a Competitive salary,We offer continued personal development. When you join Guerbet, you :Are choosing a global leader with recognized expertise in diagnostic and interventional imaging, Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient’s life all over the world,Are joining a company where we value diversity of talents coming from various horizon.We # Innovate # Cooperate # Care #Achieve at Guerbet. Guerbet is an Equal Opportunity Employer. As an organization, we believe that no individual should be discriminated against because of their differences, which includes the following: age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other basis as protected by federal, state, or local law. Guerbet is committed to diversity, equity, and inclusion.Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to View email address on click.appcast.io or you can also call this number View phone number on click.appcast.io