Careers

We rely on the expertise and enthusiasm of our employees to deliver on our promises to customers and shareholders.

 

Our close-knit, creative team strives for excellence in everything we do, and comprises professionals that specialize in:

  • Research and Development
  • Product Development
  • Engineering
  • Field Clinical Support
  • Regulatory Affairs
  • Quality Systems
  • Manufacturing & Production
  • Quality Control
  • Clinical Affairs

If you think you have the skills and attitude to enhance our company we want to hear from you. A resume and a letter outlining how you think you can contribute to our efforts may be sent to careers@neovasc.com.

Current Opportunities in New Brighton, MN, USA

 

Design Quality Engineer

The Design Quality Engineer works across all stages of the product life cycle on Neovasc projects and commercial product in accordance with state-of-the-art practices, across the domains of, Risk Management, Design Controls and Human Factors/ Usability Engineering. Provide effective support for multiple projects, balancing priorities and resources appropriately to enable the business programs. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

Clinical Study Manager

The Clinical Study Manager is responsible for the execution of high quality clinical studies and will focus on study management activities to meet study objectives. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

Principal Clinical R&D Engineer

The Principal Clinical R&D Engineer is responsible for understanding the clinical disease states and conditions treated by Neovasc products, translating clinical and user needs into product/engineering requirements, and evaluating the safety and performance of products to ensure clinical and user needs are met. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

Principal Product Development Engineer (Transcatheter Valves)

The Principal Product Development Engineer is responsible for Neovasc transcatheter valve design and development, and ensuring the safety and efficacy of Neovasc medical device products, while adhering to the necessary quality and regulatory requirements. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

Principal Product Development Engineer (Stent/Frames) (Minnesota)

The Principal Product Development Engineer is responsible for Neovasc transcatheter valve design and development, and ensuring the safety and efficacy of Neovasc medical device products, while adhering to the necessary quality and regulatory requirements. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

 

Current Opportunities in Vancouver, BC, Canada

 

Production Quality Engineer

The Production Quality Engineer works across all stages of the product life cycle on Neovasc projects and commercial product in accordance with state-of-the-art practices, across the domains of, Production and Process Controls, Supplier Controls and Risk Management, including human factors engineering for production. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

Principal Product Development Engineer (Transcatheter Valves)

The Principal Product Development Engineer is responsible for Neovasc transcatheter valve design and development, and ensuring the safety and efficacy of Neovasc medical device products, while adhering to the necessary quality and regulatory requirements. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com

 

QC & Supplier Quality Specialist

To perform incoming, in-process and final inspection products (Tiara & Reducer) in accordance with the Quality Management System. Support the Manager, QC & Supplier Quality with supplier quality and biological safety related activities. If you feel you meet these requirements and those set out in the complete job description, we welcome you to submit your resume and cover letter to: careers@neovasc.com