Job Description :
Job information Compliance Specialist (Hybrid) from the Company Kardium Inc., this latest Compliance Specialist (Hybrid) job vacancy is located in the city Hybrid work in Burnaby, BC. This latest job opening is open to job seekers who have the latest education / graduate . Job Vacancies in this Administrative field have been opened and published up to the specified time.
Job Responsibility:
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 pivotal clinical study and our focus is on regulatory approvals and commercial launch. This is an exciting and significant milestone in our journey to bring this ground-breaking technology to patients. Kardium has a unique opportunity for a Compliance Specialist. As a member of the Quality Assurance (QA) Team, the Compliance Specialist will provide support to the maintenance of Kardium's Quality Management System (QMS). The position reports to the Director of Compliance and Quality Improvement. Please note, this opportunity is a hybrid work arrangement, located in Burnaby, BC. Meaningful work you will be a part of Your responsibilities will include:- Acts as a member of the internal audit team performing audits of the QMS system, including assisting with planning, preparing reports, and other audit documentation, and performing follow-up activities
- Performs assessments of investigation, corrective and preventative actions, and effectiveness checks, as needed.
- Performs supplier qualification, monitoring and part certification activities, including site audits
- Assists in the development and delivery of QMS training and other training to employees, to ensure compliance with all applicable standards and regulations
- Assists with development and assessment of QMS performance metrics
- Assists with Document Management activities, as needed. Assists with external audits and regulatory inspections.
- Performs any other QA tasks, as required
- Bachelor's degree, preferably in a technical/science field, or equivalent combination of education and experience
- Three to five years' QA experience in a manufacturing environment
- Strong working knowledge of ISO 13485 and FDA QSR or ISO9001 in a regulated industry
- Experience with electronic document and electronic record management systems
- Previous experience in auditing techniques desirable
- Strong analytical skills and critical thinking
- Effective written & verbal communication and technical documentation skills
- Excellent computer skills (MS Office, Excel)
- Organized and detail-oriented
- Willingness to travel occasionally.
- Excellent interpersonal skills
- Ability to work effectively as part of a team and collaborate with staff at all levels
- Flexible and adaptable to take on additional responsibilities as appropriate
- $70,000 - $94,000 (CAD Annually)
More Information
- Salary Negotiable
