Regulatory Compliance Engineer: Medical Devices & Audits in Halifax

Regulatory Compliance Engineer: Medical Devices & Audits in Halifax

Halifax Full-Time 82800 - 101200 $ / year (est.) On-site
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At a Glance

  • Tasks: Ensure digital products meet global regulatory standards and lead audits for compliance.
  • Company: Join ResMed, a leader in medical technology focused on patient safety.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and patient care.
  • Why this job: Make a difference in healthcare by ensuring product quality and safety.
  • Qualifications: Experience in regulatory compliance and strong analytical skills.

The predicted salary is between 82800 - 101200 $ per year.

Res Med is seeking a Compliance Engineer to partner with engineering managers and scrum teams to build and maintain regulatory-compliant digital products.

You will apply knowledge of global standards and lead audits across MDR, SOC2, MDSAP, and related frameworks while supporting product design with compliant lifecycle practices.

The role emphasizes technical diligence, risk assessment, and clear reporting to ensure patient safety and product quality in a complex regulatory landscape.

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Regulatory Compliance Engineer: Medical Devices & Audits in Halifax employer: ResMed Inc

ResMed is an exceptional employer that champions innovation and collaboration within a diverse and inclusive culture. As an Information Security Specialist, you'll have the opportunity to work with cutting-edge technologies while contributing to meaningful health solutions on a global scale. With a commitment to employee growth and a supportive environment, ResMed empowers you to thrive in your career while making a positive impact on the world.

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Contact Details:

ResMed Inc Recruitment Team

We think you need these skills to ace Regulatory Compliance Engineer: Medical Devices & Audits in Halifax

Regulatory Compliance
Knowledge of Global Standards
Audit Management
MDR (Medical Device Regulation)
SOC2
MDSAP (Medical Device Single Audit Program)
Risk Assessment