Be part of a team that is transforming care for people with heart and vascular disease
Innovation is at the core of our ethos. It drives our mission to deliver transformative care. We are committed to the highest quality in all that we do through collaboration among our highly skilled, experienced professionals.
Every team member is greatly valued and shares the vision of significantly improving treatment paradigms. We lean on each other, support one another and hold ourselves accountable to each other. Every member of our team is a key contributor to our success.
Taking care of our team
We appreciate and recognize the brilliance of our team members.
Competitive benefits and perks are just two of the ways that we show our appreciation.
Comprehensive health care options
401(k) with available Roth contributions
Commuter & transit program
Paid time off + 11 company holidays annually
Free coffee, tea, fruit and snacks
Join us in transforming care for people with heart and vascular disease.
Manufacturing Technician Major Duties and Responsibilities Responsibilities will include, but not be limited to: Manufacture prototypes, pre-clinical and clinical units. Includes stent preparation, cleaning, and coating, catheter preparation and stent mounting, device inspection, and packaging Perform preventive maintenance as required for production equipment Organize and assemble materials and product shipments to support the commercial and […]
Contract Specialist (Part-Time) Major Duties and Responsibilities Responsibilities will include, but not be limited to: Communicating with employees from various departments, you will prepare and review drafts or amendments of Consulting, Service, Supplier, Advisor, License, Clinical Trial, Non-Disclosure, and other types of agreements using approved templates and prioritizing each to signature ready status Maintain and […]
The Regulatory Affairs Specialist supports the regulatory activities required for global market entry and patient access for Elixir Medical’s growing product portfolio. In this role they will contribute to the development and updating of regulatory strategies, submission, and documents based upon regulatory changes. This position performs specialized level work assignments in the evaluation, preparation, and submission of documentation for worldwide regulatory registrations, ensuring products and procedures comply with regulatory requirements.