Quality Control Technician

**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 talented team of innovative, and highly collaborative people. You’re also joining a community that includes thousands of physicians worldwide who use Clarius to deliver better patient care - over two million high-definition exams have been performed using Clarius And you’re joining a thrice certified Great Place to Work

**Your Role**

As a Quality Control Technician at Clarius, you’ll play a key role in ensuring the safety, accuracy, and performance of our ultrasound devices. Collaborating with our production, engineering, and quality teams, you’ll inspect and test components and finished products to verify they meet stringent regulatory and internal standards.

You’ll uphold our commitment to excellence through precise documentation, incoming inspection, root cause analysis, and support for continuous improvement initiatives. With your technical expertise, problem-solving mindset, and keen eye for detail, you'll help ensure every product reflects the high standards Clarius is known for.

This challenging and rewarding role offers autonomy and the opportunity to contribute to impactful projects within our quality team.

**Your Responsibilities Include**:

- Receiving inspection control for raw material, part fabrication, sub-assembly, and final assembly goods.
- Conduct First Article Inspections (FAI) in accordance with engineering drawings and specifications.
- Create and manage NCRs (Non-Conformance Reports) and CAPAs (Corrective and Preventive Actions) related to incoming inspections and production.
- Coordinate maintenance and calibration of all critical production and inspection equipment.
- Work with Manufacturing Engineering to identify and resolve quality issues and support continuous improvement.
- Assist with internal quality documentation updates and process audits.

**Your Experience so Far**
- A diploma or degree in Electronics, Biomedical Engineering, or a related technical field.
- 3+ years of experience in quality control or manufacturing of electronic or medical devices.
- Previous experience in technical writing, such as creating product manuals or inspection documentation.
- Familiarity with ISO13485, QMS/ERP systems, and regulatory standards for medical devices is an asset.
- Strong analytical and problem-solving skills.
- Comfortable performing routine, scheduled tasks with consistency and attention to detail.
- Excellent documentation and communication abilities.

This is a **full-time, permanent position**. The salary range for this role is **$56,000 - $66,000 CAD**.

**More Reasons to Consider**:
**Certified Great Place to Work**: Acknowledged and certified as an exceptional workplace that fosters trust, values employees, and cultivates a positive and inclusive culture.

**Volunteer Days**: Give back to any cause close to your heart by getting paid to volunteer during the working day.

**Professional Development** **Program**: Company provided finance to attend programs/seminars/conferences and courses of your choosing.

**Working Space**: You’ll love our new office. Equipped with everything needed for you to succeed as well as sit/stand desks, a wellness room, a stocked kitchen, and lots of outdoor amenities for summer activities. Our campus also has a day-care facility and a free on-site gym and is SkyTrain station adjacent.**Requirements**:

- A diploma or degree in Electronics, Biomedical Engineering, or a related technical field.
- 3+ years of experience in quality control or manufacturing of electronic or medical devices.
- Previous experience in technical writing, such as creating product manuals or inspection documentation.
- Familiarity with ISO13485, QMS/ERP systems, and regulatory standards for medical devices is an asset.
- Strong analytical and problem-solving skills.
- Comfortable performing routine, scheduled tasks with consistency and attention to detail.
- Excellent documentation and communication abilities.
- Availability to work 100% on-site at our Vancouver office.