QMS Specialist: Medical Devices & Regulatory Compliance

Oticon Medical; Nice; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Oticon Medical in Vallauris (Sophia Antipolis), France, seeks a QMS Specialist to maintain and improve its Global Quality Management System and ensure regulatory compliance.

Reporting to the QA Manager, you will drive quality processes across the organization, participate in audits, support CAPA and change control, and train staff. Fluent in French and English, you bring 3–5 years in QA or regulatory affairs in medical devices.

Qualifications

• Bachelor's degree or higher in engineering, life sciences, or related field.
• 3–5 years of experience in Quality Assurance or Regulatory Affairs, preferably in medical devices or pharmaceutical industry.
• Good understanding of quality systems and regulatory standards.
• Structured, detail-oriented, and proactive approach.
• Strong communication, leadership, teamwork skills, and solution-oriented mindset.
• Fluent in French and English.

Responsabilités

• Support the maintenance and continuous improvement of the Global Quality Management System (QMS).
• Ensure compliance with applicable regulatory requirements (ISO 13485, MDSAP, MDR 2017/745).
• Review and update QMS procedures and documentation.
• Participate in internal and supplier audits.
• Support external audits.
• Assist in CAPA management, change control, and non-conformity handling.
• Contribute to training activities related to QMS for employees.
• Prepare quality reports and provide transparency on quality performance.
• Collaborate with cross-functional teams to ensure quality standards are met.

Connaissances

Quality Assurance

Regulatory Affairs

QMS

Auditing

Cross-functional collaboration

Formation

Bachelor's degree in engineering/life sciences

Description du poste

Oticon Medical in Vallauris (Sophia Antipolis), France, seeks a QMS Specialist to maintain and improve its Global Quality Management System and ensure regulatory compliance.

Reporting to the QA Manager, you will drive quality processes across the organization, participate in audits, support CAPA and change control, and train staff. Fluent in French and English, you bring 3–5 years in QA or regulatory affairs in medical devices.