Responsibilities :
* Collaborate in maintaining the quality system documentation processes and procedures adopted by the company.
* Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence.
* Coordinate and support the preparation of software technical documents appropriate for regulatory submissions.
* Support the regulatory submissions for market authorization for medical device products.
* Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures.
* Facilitate the approval process for software releases.
* Disseminate knowledge about the Quality System and regulatory requirements.
* Oversee post-market surveillance activities related to medical device products.
* Offer guidance and mentorship to QARA team members at lower levels.
Job Benefits :
* Permanent Contract.
* 3 days a week working from home.
* Flexible Schedule.
* Multicultural and friendly team.
* Exciting opportunities for professional development.
* Ongoing training.
* Multiple Social benefits: Canteen, health insurance, nursery check, English training...
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