Software Verification Team Lead, MDS Release (Hybrid) at Kardium Inc
Burnaby, BC, Canada -
Full Time


Start Date

Immediate

Expiry Date

14 Nov, 25

Salary

116000.0

Posted On

14 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

Your opportunity
By joining the Kardium team, you can help make a difference in the lives of millions around the world. We have developed a ground-breaking medical device for the diagnosis and treatment of the most common heart rhythm disorder, atrial fibrillation – which can cause stroke, heart failure, and other heart-related complications.
Kardium’s mission is to deliver the best treatment for atrial fibrillation. To achieve this, we have developed The Globe® Pulsed Field System – we have a fantastic technical team that has developed a product with strong, unique, and customer-valued differentiators versus other solutions on the market. We have built connections with key opinion leaders who are already using the Globe System and are helping to tell our story.
We have now completed our regulatory approvals and on track for commercial launch. This is an exciting and significant milestone in our journey to bring this ground-breaking technology to patients.
The Software Verification Team is seeking a MDS Release Team Lead to support verification and validation activities for Kardium’s flagship product. This role will be critical in ensuring that the Globe System and associated software comply with industry regulations. The MDS Release role will lead the efforts for Globe Software releases and patches to ensure that our product software is regulatory compliant and supports our commercial sites. The role will have a pivotal impact on the quality and frequency of Globe Software releases, ensuring that verification is done early and efficiently in the release cycle.
Please note, this opportunity is a hybrid work arrangement, located in Burnaby, BC.
Meaningful work you will be a part of

Responsibilities
  • Bachelor of Science or Engineering degree
  • Practical, hands-on experience in design or Software test engineering
  • Multidisciplinary understanding of medical device system
  • Practical knowledge of medical device regulations and industry standards (FDA, IEC 62304, ISO 14971, etc.).
  • Excellent communication and documentation skills
  • Flexible and adaptable to take on additional responsibilities as appropriate
  • Familiarity with software development lifecycles (SDLC) and Agile methodologies
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