Compliance Specialist

**A Career at Clarius**

Today, as many as 25 million medical professionals globally don’t have access to medical imaging, which is proven to improve patient care and reduce healthcare costs. That’s why we’re on a mission to make medical imaging accessible everywhere by delivering high-performance, affordable, and easy-to-use solutions powered by artificial intelligence and connected to the cloud.

By making Clarius your next career move, you’re joining a team of 140+ people who are talented, innovative, and highly collaborative. You’re also joining a community that includes thousands of physicians worldwide who use Clarius to deliver better patient care And you’re joining a thrice-certified Great Place to Work

**Your Role**

Are you eager to launch a career in medical device compliance? Clarius Mobile Health Corp. is looking for a detail-oriented and driven Medical Device Compliance Specialist to join our QA/RA team. Actively support compliance efforts to ensure Clarius meets all necessary regulatory requirements and standards. You’ll join Clarius Mobile Health’s QA/RA team, where you’ll contribute directly to our mission by ensuring our products meet high regulatory standards This is an ideal opportunity to gain hands-on experience in the fast-paced medical device industry, building skills that make a real impact. This role is your chance to build a solid foundation in medical device compliance within a supportive, growth-focused environment.

**Your Responsibilities Include**:

- Compliance Monitoring: Stay on top of updates to regulations and standards from FDA, ISO, and other regulatory bodies, helping keep Clarius in full compliance.
- Quality Management System (QMS) Support: Help maintain and continuously improve Clarius' QMS to meet ISO 13485 and other essential standards.
- Internal Audits: Assist in internal audit processes, ensuring compliance across all departments.
- Non-Conformance Reporting: Participate in corrective action planning and support implementation efforts.
- Deliver Training: Contribute to creating compliance training programs.
- Coordinate Efforts: Work across teams to ensure smooth process implementations.
- Gather Regulatory Insights: Research and provide insight into emerging regulatory trends.
- Drive Improvement: Support initiatives to streamline our compliance efforts.

**Your Experience So Far**:

- Post-secondary education preferably in Quality Management, Sciences, or a related field.
- 0-2 years of experience in Quality Management System or related field within the healthcare industry.
- Understanding of 21 CFR 820 and/or ISO 13485.
- Strong attention to detail and organization skills.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in Microsoft Office Suite.
- Ability to manage multiple tasks and meet deadlines.

**Location and Compensation**:
Based in Vancouver, BC, with a hybrid work option. The salary range for this role is set at $60,000 - $70,000.

**More Reasons to Consider**:
**Flexible Hours & Hybrid Model**: Embrace work-life balance with flexible hours and a hybrid work model that suits your lifestyle.

**Benefits from Day 1**: Get full access to your comprehensive benefits package made available from your very first day.

**Volunteer Days**: Make a difference with paid volunteer days during working hours, supporting causes that matter to you.

**Professional Development** **Program**: We're big fans of continuous learning, and we invest in your growth with financial support for programs, seminars, conferences, and courses.

**Workspace**:Our modern office features sit/stand desks, various health & wellness facilities, a stocked kitchen, outdoor amenities, on-site daycare, enclosed parking, a free on-site gym and close proximity to a SkyTrain station.