What are the responsibilities and job description for the Verification Specialist position at Sentec?
At Sentec, we are committed to developing innovative medical solutions that support the wellbeing of individuals worldwide. We are seeking a highly skilled Validation Engineer to join our team and contribute to the development of respiratory care products.
This role involves collaborating with cross-functional teams to ensure compliance with medical device quality and regulatory standards. The successful candidate will be responsible for developing and executing verification and validation plans, protocols, and procedures for respiratory therapy medical devices.
- Develop and execute verification and validation plans, protocols, and procedures for respiratory therapy medical devices.
- Collaborate with product development teams to review design inputs and outputs and ensure all V&V activities and outcomes are correctly traced to product requirements.
- Execute performance, system, and product testing to ensure design inputs meet device requirements and user needs.
- Work closely with design and quality teams to resolve any nonconformances identified during V&V activities.
