Warehouse Project Coordinator

At 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 Youtube

WHAT WE ARE LOOKING FOR

The Warehouse Project Coordinator will operate 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. The Warehouse Project Coordinator is accountable for restoring and sustaining full compliance of the warehouse to cGMP (21 CFR Parts 210/211) and Good Distribution Practice (GDP) standards, remediating recent inspection findings, and embedding robust quality systems and lean operations. This role leads warehouse projects focused on compliance strategy, continuous improvement, and audit readiness while partnering with Quality, Production, and Supply Chain to ensure safe, compliant, and efficient material flow from receipt through distribution.

YOUR ROLE

Own and execute the warehouse compliance remediation plan addressing FDA Form 483 and Warning Letter observations; drive timely, effective CAPA with documented effectiveness checks. Establish, maintain, and continuously improve written procedures for receipt, identification, storage, handling, sampling, testing, approval/rejection, and distribution of components and drug products per 21 CFR 211.80, 211.82, 211.84, 211.142, and 211.150. Implement and sustain physical and systematic status labeling and physical segregation for quarantine, approved, rejected, returned, and recalled materials; ensure lot/batch traceability to enable rapid recalls. Ensure storage under appropriate temperature, humidity, and light conditions supported by stability data; manage temperature excursion evaluation and documentation. Strengthen GDP practices for distribution, including FEFO/FIFO stock rotation, route qualification, and carrier oversight; verify proper transport conditions and chain of custody. Own warehouse training program: role-based competency, cGMP/GDP, data integrity, and documentation practices; ensure training effectiveness and periodic assessment. Lead self-inspection program and audit readiness, coordinate responses to regulatory inspections and partner audits. Drive standard work, 5S, visual management, and waste elimination to improve Safety, Quality, Delivery, Cost (SQDC) while maintaining compliance. Partner with Quality to trend deviations, change controls, complaints, returns, and recalls; implement risk-based preventive actions aligned with ICH Q9 principles

YOUR BACKGROUND

Required Qualifications Bachelor’s degree in Engineering, Supply Chain, Life Sciences, or a related field 7+ years of experience in GMP-regulated warehouse/materials management, including 3+ years leading compliance remediation or continuous improvement initiatives Expert knowledge of 21 CFR Parts 210/211 (Subparts E, H, J), GDP guidelines, and USP storage and shipping practices Demonstrated experience with temperature mapping/qualification of storage areas and excursion management Strong CAPA, change control, deviation investigation, and risk management skills; proven audit readiness leadership Proficiency with WMS/ERP systems and validated monitoring systems; strong data integrity and documentation practices Excellent communication, cross-functional collaboration, and stakeholder management skills Preferred Qualifications Familiarity with ICH Q9 and ISPE guidance for controlled temperature chambers and quality systems Lean/Six Sigma certification (Green Belt or Black Belt) Experience with Sales & Operations Planning or Integrated Business Planning (IBP) processes in a GMP-regulated environment Experience working in a multi-site or global supply chain environment with complex distribution networks Reason to join US Much 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. 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 numberView phone number on click.appcast.io #J-18808-Ljbffr Guerbet