Would you like to contribute to improving the quality of life of people with hearing loss?
At Oticon Medical, we develop, produce and market bone-anchored hearing systems. At our site ITSA Medical in Vallauris (Sophia Antipolis), in the south of France, we specialize in the production of active implantable class III implants and soon also worldwide distribution of the company’s full product portfolio.
We are now seeking a QMS Specialist to support and maintain our Quality Management System (QMS) and ensure compliance with global regulatory requirements. Reporting to the QA Manager, you will play a key role in implementing, improving and merging local and global quality processes across the organization.
Close collaboration with Operations, Regulatory Affairs, and Product Care teams
Interaction with notified bodies and auditors during inspections
Bachelor’s degree or higher in engineering, life sciences, or related field
Minimum 3–5 years of experience in Quality Assurance or Regulatory Affairs, preferably within 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