About this role
KARL STORZ France is looking for an Apprentice in Quality and Regulatory Department : Contribute to regulatory intelligence and monitoring (ISO standards, European regulations, FDA requirements, etc.). Participate in the maintenance and improvement of the Quality Management System (QMS) in accordance with ISO 13485 . Contribute to the drafting, review, and updating of quality procedures and documentation .
Participate in internal audits and support the preparation of external audits and inspections .Monitor quality performance indicators (KPIs) and contribute to continuous improvement initiatives . Participate in the management of customer complaints, medical device vigilance (materiovigilance), and product or batch recalls . Support Quality and Regulatory Affairs projects and other compliance-related activities as required.
Required profile is : Currently pursuing a Bachelor's or Master's degree in Quality Management, Regulatory Affairs, Biomedical Engineering, Life Sciences, or a related field . Strong interest in medical device regulations , quality systems, and compliance requirements. Basic knowledge of ISO 13485 , EU Medical Device Regulation (MDR), or healthcare industry regulations is an advantage.
Good analytical and problem-solving skills with attention to detail and accuracy. Strong written and verbal communication skills in French and English . Proficiency in Microsoft Office applications (Excel, Word, PowerPoint); knowledge of SharePoint or Power BI is a plus.
Ability to work independently while collaborating effectively within a cross-functional and international team environment. Organized, proactive, and eager to learn in a dynamic Quality and Regulatory Affairs environment Your Benefits Health insurance Vacation days (25 days /year) Additional days (between 10 or 13 days /year) Lunch vouchers Opportunity to work in an international and well-known company A supportive team and modern working-environment