Supply Chain Quality Analyst

¬† [[extTitle]] ¬† 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 ‚Äč‚Äčthat 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 www.guerbet.com and follow Guerbet on Linkedin, Twitter, Instagram and Youtube ¬† WHAT WE ARE LOOKING FOR The Supply Chain Quality Analyst will operate in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization‚Äôs framework, company‚Äôs procedures, and the defined scope of responsibility the role is accountable for. Leads coordination and execution of inbound raw material and finished goods batch release processes in a GDP/cGMP environment. Ensures clear tracking of release steps, timely documentation, and operational integrity across Supply Chain, QC, QA, and Manufacturing. Restores batch release compliance and maintains site inspection readiness. YOUR ROLE Owns end-to-end batch release lifecycle: inbound raw materials, intermediates, and finished goods‚ÄĒreviewing batch records, Certificates of Analysis, and ensuring alignment with cGMP and GDP requirements. Coordinates cross-functionally (QC, QA, Manufacturing, Logistics) to resolve hold-ups, reconcile discrepancies, and communicate release status to stakeholders. Monitors batch release KPIs (e.g., release cycle time, documentation completeness, hold-to-release ratio); drives process improvements using CAPA methodology and procedural optimization. Facilitates GMP alignment at the warehouse‚Äďproduction boundary (label control, status segregation, quarantine, FEFO/traceability) Escalates nonconformances and deviations impacting release timelines, initiates investigations according to SOPs. Ensures strict compliance with data integrity (ALCOA+), maintaining electronic and paper records per 21 CFR Part 11, GDP, and internal Quality Systems. Reviews and updates SOPs/WIs related to batch release and material inbound quality release; supports training and competency assessments across teams. Performs ad-hoc quality checks (e.g., QC results, GMP documentation) and collaborates on material review board/QA disposition meetings. Ensures timely release of inbound raw material and excipient batches to prevent downstream manufacturing delays, coordinates laboratory escalation and deficiency resolution. Performs other duties as assigned by management. YOUR BACKGROUND Required Qualifications Bachelor‚Äôs degree in Life Sciences, Pharmacy, Chemistry, Engineering, or equivalent. 3+ years‚Äô experience in pharmaceutical batch release or quality systems within a cGMP/GDP-regulated site. Proven experience facilitating inbound raw material release and finished goods batch release processes. Strong knowledge of FDA 21 CFR 210/211, 21 CFR Part 11, and EU GDP requirements. Proficient in managing cross-functional communication, deviation escalation, and deviation/CAPA systems. Familiarity with ERP/WMS documentation management and electronic quality systems. Preferred Qualifications APICS certification, Lean/Six Sigma experience. Record of leading QA projects, batch release continuous improvement, or metric-driven performance programs. ¬† 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‚Äôs 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 careers@guerbet.com¬† or you can also call this number¬†+19843443717