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The Quality Assurance Engineer will monitor medical devices post-market, analyze data for safety issues, perform risk assessments, and ensure compliance with regulatory standards.

The Territory Manager will achieve sales objectives by engaging peripheral interventionalists, managing accounts, collaborating with departments, and supporting training initiatives.

The Senior Process Development Engineer will optimize manufacturing processes for neurovascular devices, ensuring efficient operations and compliance with regulatory standards.

The Paralegal role involves supporting legal processes, maintaining records, managing compliance, and assisting with corporate filings and documentation management.

The Grants Manager will oversee US Grants and Investigator Initiated Research (IIR) submissions, manage budgets, track milestones, and liaise with internal stakeholders and requesting sites, ensuring compliance and communication throughout the process.

The Senior Quality Engineer will support production quality and supplier activities, improve manufacturing processes, and ensure compliance with quality standards in neurovascular medical device production.