QMS Specialist / Spécialiste QMS

Because sound matters

Oticon Medical is a global company in implantable hearing solutions, dedicated to bringing the power of sound to people at every stage of life. For more than a decade, we have made bone anchored hearing systems more accessible by simplifying the treatment for physicians, audiologists, and patients alike.

We believe that patients and hearing care professionals should be able to choose the best possible solution at any time along the patient journey. We call it “Freedom of Choice” and it has always been paramount to Oticon Medical. This is the reason why our solutions are designed to be compatible whenever possible. As a result, an implant from Oticon Medical stands as a true testament to our unwavering lifelong support.

We work collaboratively with professionals to ensure that every solution we create is designed with our users’ needs in mind. We have a strong passion to provide innovative solutions and support that enhance quality of life and help people live life to the fullest – now and in the future.

Because we know how much sound matters.

QMS Specialist

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.

Main responsibilities

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

Key Working Relationships

Close collaboration with Operations, Regulatory Affairs, and Product Care teams

Interaction with notified bodies and auditors during inspections

Profile

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

Apply now »