Quality Engineer

Title : Quality Assurance Engineer Location : Paris, France ✉️ Contact : kristinaelemed.eu Are you passionate about quality assurance and eager to make a difference? Are you ready to team up with partners who share your drive for excellence? The Company This company believes in the power of innovation to make a real impact on patient lives so are developing groundbreaking technology that transforms invasive medical devices into connected healthcare solutions. They may be a small business but they are having HUGE impact - and you could too If you dream of working in a fun and engaging environment where your ideas are valued and love the idea of being part of a community that prioritizes employee happiness and personal growth - this is the place for you. The Opportunity This is not just a job; it’s a chance to create meaningful change in the medical device industry. You’ll have the opportunity to mentor others and lead initiatives that directly impact patient care. As Quality Assurance Engineer, no day will be the same as you will have a wide range of responsibilities from QMS maintenance to risk management to supporting design & development projects. You will be at the forefront of the manufacturing and development processes, ensuring that quality and compliance are prioritized in every project and play a crucial role in maintaining the Quality Management System (QMS) as well as supporting various teams in meeting regulatory requirements. Your responsibilities: Maintain and ensure the QMS is effective, compliant, and fit for purpose to meet Sensome’s needs. Participate in risk management activities to identify and mitigate potential issues. Generate, review, and edit procedures and other essential documentation to support quality standards. Facilitate and participate in activities to resolve nonconformities, driving corrective actions and preventive measures. Conduct internal and external audits to ensure compliance with regulatory and quality standards. Assist the manufacturing team in document management and support the regulatory team in navigating the MDR. Stay updated on changes in the regulatory landscape, providing guidance and recommendations to the team. Work collaboratively with interdisciplinary teams to tackle challenges and enhance quality processes. If you’re an ambitious professional with at least 3 years of experience in quality management in the medical device field, we want to hear from you. Bring your expertise, your innovative spirit, and your commitment to excellence. Let’s build something extraordinary together Your qualifications: 3 years of Quality experience in the medical device industry Engineering degree Fluent French and English ✉️ Interested to explore this further? Please send your CV to kristinaelemed.eu to arrange a confidential career discussion. Would you like to find out more about our open opportunities? Visit https://www.elemed.eu/vacancies/ Please note: Only candidates meeting the requirements set out in the role profile above, will be considered in the application process. Due to the high volume of applications we receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful. ___________________________________________________________________ Elemed is Europe’s leading MedTech technical recruiter. We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow. At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices. ⚖️ We are an equal opportunity employer and value diversity at our company . We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

Location: Paris, FR

Posted Date: 1/17/2025