What are the responsibilities and job description for the Quality Assurance Lead for Respiratory Medical Devices position at Sentec?
As a Quality Assurance Lead for Respiratory Medical Devices at Sentec, you will be responsible for 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.
Responsibilities:
- Develop and execute quality assurance plans, protocols, and procedures for respiratory therapy medical devices.
- Collaborate with cross-functional teams to ensure compliance with medical device quality and regulatory standards.
- Work closely with design and quality teams to resolve any nonconformances identified during V&V activities.
Sentec utilizes 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.
