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Regulatory Compliance Specialist for Global Medical Devices
hace 1 día
At Edwards Lifesciences, we're driven by a passion to improve patient lives. As a global leader in structural heart innovation, we offer rewarding opportunities and exciting challenges in a dynamic and friendly work environment.
About the RoleThis is a unique career opportunity for an Associate Specialist, Quality Compliance role in Spain-Valencia. You'll bring your expertise and passion for problem-solving to partner with various teams to influence decision-making for a product's entire lifecycle.
Your key responsibilities will include:
- Fulfilling applicable medical device regulations, including ISO13485 and other relevant requirements for designated complaint handling units.
- Evaluating events for reportability to competent authorities.
- Investigating complaints with the support of higher-level team members or managers.
We need someone with:
- A Bachelor's Degree in a related field.
- 1 year experience in complaint handling or similar roles.
- Experience working in a medical device (cardiovascular, endovascular, or other critical care/surgical products), healthcare, or a related environment.
We offer a competitive compensation package, flexible working hours, remote working options, pension plan, life insurance, medical plan, meal vouchers, service awards, enhanced leave benefits, employee stock purchase programme, employee assistance programme, comprehensive wellness programme, and much more.
Join Our TeamAt Edwards Lifesciences, we foster a diverse and inclusive work environment where all employees can grow, personally and professionally. We offer on-the-job development, training opportunities, and the support and guidance provided by dedicated employee groups.
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