Main Activities Supplier Management: Maintain and implement supplier management processes to ensure strong and effective relationships.Selection and Evaluation: Participate in the selection, qualification and periodic evaluation of suppliers according to established procedures.Complaints and Notifications: Ensure the processing and follow-up of supplier complaints and change notifications within the required timeframes.Assessment Meetings: Organize and participate in change impact assessment meetings.Audits: Plan, organize and carry out supplier and distributor audits.Quality: Handle quality events (non-conformity, OOS, change control, CAPA) in collaboration with other departments.Continuous Improvement: Lead problem-solving groups and support continuous quality improvement projects.Internal Communication: Feed back information from the various departments within the Quality Department.Quality Referent: Intervene on projects as a quality referent, review new design specifications and provide your input on component quality and manufacturing feasibility.Investigations and Corrective Actions: Investigate supplier material failures and develop corrective action plans if necessary.Acceptance Criteria: Develop material acceptance criteria and activities. ProfileMastery of Quality Standards ISO 9001 & 13485Knowledge of MDRCertified Lead Auditor 13485Knowledge of Quality tools (5P, 5M, 8D,...) and risk analysis methodsEnglish: Good comprehension and writing skills (minimum level B2)Basic training: CFC or equivalentProfessional experience required: Minimum 5 years of experience in quality in the pharmaceutical and/or medical device industryAutonomous, rigorous, with a strong team spirit jid353d5c5a jit0311a