← Back to opportunities
Ensure product compliance with applicable standards and regulations. Prepare and maintain technical documentation according to MDR requirements. Maintain Design History Files (DHF) and controlled documents. Collaborate with cross-functional Nipro teams in EMEA and Japan. Interface with contract developers and manufacturers in Eur...
About the Role
You will be working in a team that ensures product compliance with relevant standards and Nipro's design and development process. This role is crucial in fostering a culture of design for compliance and quality, supporting continuous improvement, and ensuring the safety and regulatory compliance of our medical devices. You will collaborate with cross-functional teams to support the development of innovative and compliant medical devices that positively impact patient outcomes.
What you’ll do
Design Compliance (40%)
Documentation Control (10%)
Collaboration and Co-ordination (20%)
Ready to Join Through a Referral?
Apply now and get connected directly with the hiring team
Apply for this Position