Quality Engineer Investigations

Missions

• Lead and coordinate the CAPA (Corrective and Preventive Actions) system
• Conduct thorough investigations and root cause analyses
• Manage non-conformance processes (NCMR) end-to-end
• Facilitate CAPA review boards and collaborate with internal and external stakeholders
• Define, implement, and monitor corrective and preventive action plans
• Track quality metrics and identify improvement opportunities
• Apply problem-solving methodologies (Ishikawa, DMAIC, Lean tools)
• Drive continuous improvement initiatives across quality processes
• Support supplier investigations and monitor supplier performance
• Contribute to internal and external audits (preparation, execution, follow-up)
• Ensure compliance with international regulations (ISO, FDA, MDR, etc.)

Profil du candidat

• Scientific degree (engineering, life sciences, pharmacy, or equivalent)
• 3-5 years of experience in Quality Assurance within a regulated environment
• Experience in medical devices or pharmaceutical industry
• Strong knowledge of ISO 13485, FDA, MDD/MDR regulations
• Expertise in CAPA, non-conformance management, and investigations
• Proficiency in root cause analysis tools and Lean methodologies
• Strong project management and prioritization skills
• Good command of quality systems and IT tools (MS Office, QMS software)
• Excellent communication and cross-functional collaboration skills
• Fluent in French and good level of English
• Analytical mindset, attention to detail, and high integrity

Conditions et Avantages

• International and high-impact working environment
• Strategic role with strong visibility within a temporary assignment
• Opportunities for professional development and growth within a defined mission