About the Company
Medtronic is a global leader in medical technology, services, and solutions. We strive to alleviate pain, restore health, and extend life for millions of people worldwide. With a strong commitment to innovation and patient care, our diverse portfolio includes products and therapies for cardiac and vascular diseases, respiratory, gastrointestinal and renal diseases, neurological disorders, and diabetes. Join our mission-driven team and contribute to groundbreaking advancements that save and improve lives every day.
Job Description
Medtronic is seeking a dedicated and innovative Biomedical Engineer to join our dynamic R&D team in Summerside, Prince Edward Island, Canada. This is an exceptional opportunity for a talented professional seeking to advance their career with a global leader. We are committed to supporting international talent and visa sponsorship will be provided for qualified candidates. The successful candidate will play a crucial role in the design, development, and testing of cutting-edge medical devices, ensuring compliance with international standards and regulatory requirements. This role offers a blend of hands-on technical work, problem-solving, and collaboration within a multidisciplinary team.
Key Responsibilities
- Design, develop, and validate medical devices and associated technologies, from concept to commercialization.
- Conduct feasibility studies, risk assessments, and design verification/validation activities.
- Perform biomechanical analysis, material selection, and process optimization.
- Collaborate with cross-functional teams including R&D, manufacturing, quality, and regulatory affairs.
- Prepare and maintain detailed technical documentation, design specifications, and test protocols.
- Ensure all designs and processes comply with relevant medical device regulations (e.g., ISO 13485, FDA, Health Canada).
- Participate in design reviews and contribute to continuous improvement initiatives.
- Support clinical trials and post-market surveillance activities as needed.
Required Skills
- Bachelor's or Master's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related field.
- Minimum of 4 years of experience in medical device design, development, or manufacturing.
- Proficiency with CAD software (e.g., SolidWorks, AutoCAD).
- Strong understanding of biomechanics, biomaterials, and medical device manufacturing processes.
- Knowledge of medical device regulations (FDA, Health Canada, CE Mark).
- Excellent problem-solving, analytical, and communication skills.
- Demonstrated ability to work effectively in a team-oriented environment.
Preferred Qualifications
- P.Eng designation or eligibility for registration in Canada.
- Experience with finite element analysis (FEA) software.
- Familiarity with sterilization methods for medical devices.
- Experience in a regulated industry environment (e.g., ISO 13485).
- Prior experience with Class II or Class III medical devices.
Perks & Benefits
- Comprehensive health, dental, and vision insurance.
- Competitive salary and performance-based bonuses.
- Generous paid time off and holidays.
- Retirement savings plan with company match.
- Tuition reimbursement and professional development opportunities.
- On-site fitness center and wellness programs.
- Employee stock purchase plan.
- Relocation assistance and full visa sponsorship.
- Hybrid work model offering flexibility.
How to Apply
Interested candidates are invited to submit their application by clicking the "Apply Now" button below. To ensure your application is considered, please include the following:
- A current resume
- A cover letter outlining your suitability for the role and your motivation for applying.
We review applications on a rolling basis and will contact shortlisted candidates for an interview.
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