Currently pursuing a degree in Engineering, Quality Management, or a related field.
Enrolled as a student for the duration of the internship program. Graduating December 2024 or later.
Maintain a minimum GPA of 3.0 or higher.
Strong interest in quality engineering within the medical device industry.
Knowledge of quality standards and regulations (e.g., ISO 13485, FDA regulations) preferred.
Detail-oriented with excellent organizational and analytical skills.
Effective communication and teamwork skills.
Responsibilities
Assist in maintaining and improving the Quality Management System (QMS) to ensure compliance with relevant standards and regulations.
Support the execution of quality control activities, including inspection, testing, and documentation of results.
Contribute to risk management activities, including the identification, assessment, and mitigation of risks associated with medical device development.
Assist in managing and organizing quality-related documentation, ensuring accuracy and compliance with established procedures.
Collaborate with the team to assess and monitor the performance of suppliers to maintain a high level of quality in the supply chain.
Participate in the investigation and resolution of quality issues through the CAPA process.
Contribute to continuous improvement initiatives by identifying opportunities to enhance processes and systems.
Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.