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p>As a key member of the organization, you'll be part of a diverse team in a dynamic, global environment. Your role involves:
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Serving as a compliance representative for the quality control department and QC Support TeamLeading deviations, CAPA, and periodic reviews related to our activitiesProviding training in CCP, CAPA, and investigationsEnsuring compliance for the QC support Group and the Quality Control DepartmentContributing to the continuous improvement of quality control support processes and proceduresReviewing and approving internal documents and agreementsParticipating in equipment and material qualificationActing as a quality project manager to proactively identify and resolve problemsCollaborating with various functions and stakeholdersServing as an expert for deviation, change control, and CAPA topics during health authority inspectionsBackup for other QC support compliance, autonomously resolve compliance issues promptly, contribute to continuous improvement using a lean process mindset, and actively participate in performance management meetings to drive improvement.
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p>qualifications
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Eng. in sciences (chemistry, biology) or 3+ years of experience in a GMP environmentMinimum 1 year expertise in the biotech industryPrecise, rigorous, and detail-orientedTeam player with the ability to collaborate across departmentsExperience in quality control and quality systemsExperience in planning tools is a plusGood knowledge of visual managementFamiliar with applicable cGMPsFluent in French and EnglishProcess-oriented with a strong customer service focusProficient in problem-solving tools and ensuring their use in the groupResult-driven with a "can do" attitudeAutonomous, reliable, and highly motivatedPositive and collaborative communication within the team and with partners/customers