What are the responsibilities and job description for the Senior Medical Device Validation Specialist position at Sentec?
The role of a Senior Medical Device Validation Specialist at Sentec involves ensuring the quality and regulatory compliance of respiratory therapy medical devices. This includes developing and executing verification and validation plans, protocols, and procedures to guarantee that design inputs meet device requirements and user needs.
Key Responsibilities:
- Develop and execute performance, system, and product testing to ensure design inputs meet device requirements and user needs.
- Collaborate with product development teams to review design inputs and outputs, ensuring all V&V activities and outcomes are correctly traced to product requirements.
- Work closely with design and quality teams to resolve any nonconformances identified during V&V activities.
Sentec is a Swiss-American medical device company specializing in respiratory care, utilizing advanced science and technologies for respiratory patients across care areas. As a key member of our team, you will contribute to the development of innovative medical solutions supporting the wellbeing of individuals worldwide.
