Senior QA Manager

Rejoignez notre client en tant que Senior QA Manager, leader clé dans l'organisation. Vous aurez l'opportunité de diriger une équipe de qualité dynamique et de bénéficier d'un environnement de travail stimulant.TâchesDiriger l'équipe QA pour assurer conformité et excellence opérationnelle.Collaborer avec les leaders pour mettre en œuvre des initiatives d'amélioration de la qualité.Gérer les audits internes et externes, en étant l'interface principale avec les autorités.CompétencesDiplôme avancé en Biologie ou Sciences Pharmaceutiques, avec 10 ans d'expérience en QA.Expertise en ISO 13485 et QMSR dans le secteur IVD.Compétences en amélioration des processus, Lean ou Six Sigma.JobdescriptionSenior Quality ManagerAs a pivotal leader within our client organization, you will serve as the Quality Management Representative for the site, providing strategic direction to the QA team and ensuring our operations remain at the forefront of industry excellence.ResponsabilityStrategic Leadership: Guide the QA team to drive compliance and operational excellence across all quality functions, including NC/CAPA, change control, risk management, and complaint handling.Operational Excellence: Partner with leadership and product segment managers to spearhead robust quality improvement initiatives and elevate overall performance.Culture Champion: Foster a high-integrity culture of quality and GMP awareness, ensuring the site consistently meets or exceeds global regulatory standards.Audit Management: Lead and coordinate all internal and external audits, serving as the primary interface for health authorities, notified bodies, and key customers.QMS Evolution: Spearhead projects to harmonize and optimize quality processes, collaborating with global QA leaders to evolve the Quality Management System (QMS).ProfileWe are looking for a seasoned leader who balances technical mastery with a strategic, value-driven mindset.Educational Background: Advanced degree (BSc/MSc or equivalent) in Biology, Pharmaceutical Sciences, or a related field.Regulatory Expertise: Deep knowledge of ISO 13485, QMSR / 21CFR820, MDSAP, and IVDD/R, specifically within the In-Vitro Diagnostics (IVD) sector.Industry Experience: At least 10 years in Quality Assurance within the medical device or healthcare industry, including hands-on IVD experience.Proven Leadership: Minimum of 8 years in a managerial role with a track record of developing high-performing, results-oriented teams.Soft Skills: Exceptional interpersonal, negotiation, and communication skills, with the ability to turn quality activities into strategic organizational value.Process Improvement: Experience in Lean or Six Sigma; a Green Belt certification is highly desirable.Project Management: Solid background in managing complex quality projects and meeting deadlines in dynamic environments.Language Proficiency: Fluency in French and English is required; a good command of German is considered a significant asset.Margot Ferraton