Enable job alerts via email!

Quality & Regulatory Coordinator

Trudell Healthcare Solutions Inc.

London

On-site

CAD 50,000 - 80,000

Full time

Yesterday
Be an early applicant

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a dedicated Quality & Regulatory Coordinator to enhance patient care through effective quality assurance practices. This role involves ensuring compliance with quality systems, managing regulatory submissions, and coordinating audits to uphold the highest standards in healthcare. Join a reputable organization that values professional development and offers a supportive environment where your contributions will directly impact the quality of life for patients. If you're passionate about quality assurance and eager to make a difference, this opportunity is perfect for you.

Benefits

Challenging careers with constant learning opportunities
Professional Development Encouraged
Employee Recognition for Milestone Anniversaries
Regular Salary Reviews
Paid Sick Days
3 weeks paid vacation to start
Health and Dental Benefits
Pension Plan
Life Insurance
Employee Assistance Plan

Qualifications

  • 3-5 years of Quality Assurance experience required.
  • Strong interpersonal and communication skills are essential.
  • Ability to work independently and handle quality issues.

Responsibilities

  • Ensure compliance with quality systems through documentation and audits.
  • Coordinate product recalls and communicate with customers.
  • Assist in regulatory submissions and maintain compliance.

Skills

Quality Assurance
Regulatory Compliance
Document Control
Internal Audits
ISO Standards
Interpersonal Skills
Communication Skills
Microsoft Office

Education

Post secondary diploma in Health Sciences
Post graduate certificate in Quality Assurance
Documented ISO certificate/training

Job description

  • Do you have an interest in the Healthcare industry and have a passion for helping people?
  • Do you consider yourself to be very organized, highly focused on details, and place a high importance on quality?
  • Do you consider yourself to be technically inclined and are able to think outside the box to resolve issues?

We at Trudell Healthcare Solutions “(THS)” are looking for an individual who is driven and shares our passion for customer excellence to contribute to the care patients receive while at the hospital, ultimately helping to improve their quality of life. If you have an interest in Quality Assurance and have responded yes to the above questions, THS currently has an exciting opportunity for you as a Quality & Regulatory Coordinator!

The Position: Ensures compliance with the company’s quality system through document control, internal audits, licensing, complaints handling and product recall administration. Maintain regulatory compliance by providing accurate, relevant and timely information for internal & external resources. Provide support for regulatory submissions as required. Contribute towards the continuous improvement of THS’ quality systems.

What We Offer

In addition to fair and equitable compensation and the excitement of working for a growing and reputable company, we offer:

  • Challenging careers that provide the opportunity to learn constantly.
  • Clear, consistent and demonstrated values.
  • Encouraged Professional Development.
  • Employee Recognition for Milestone Anniversaries.
  • Regular Performance Appraisals.
  • Regular Salary Reviews.
  • Paid Sick Days.
  • 3 weeks paid vacation to start.

Comprehensive Group Family Benefits Including

  • Health and Dental Benefits.
  • Pension Plan.
  • Life Insurance.
  • Employee Assistance Plan.
  • Disability Insurance.
  • Out of Country Insurance Coverage.

Key Responsibilities

Quality Assurance:

  • Ensure proper documentation and resolution of product complaints.
  • Review quality control inspections and authorized releases of medical devices and natural health products.
  • Ensure proper documentation and resolution/closure of product complaints.
  • Record non-conformances, assist in corrective action implementation, and ensure resolution/closure.
  • Assist operations to identify and resolve product safety and quality concerns.

Quality Management

  • Perform internal audits, assist with external audits and Health Canada Inspections as required.
  • Coordinate improvement, implementation, and maintenance of ISO 13485 procedures.
  • Coordinate improvement, implementation, and maintenance of Natural Health product procedures.
  • Identify & document required preventive corrective actions (CAPA), assist in implementation and complete verifications.
  • Participate in Risk Analysis and development of Risk Management plans for medical devices licensed by THS.
  • Review and maintain technical file for medical devices licensed by THS.

Regulatory & Compliance

  • Complete annual review of Health Canada (HC) Medical Device Licenses, HC Medical Device Establishment License, and Natural Health product site license.
  • Process the Medical Device Establishment License renewal(s).
  • Participate in regulatory projects related to new product launch under THS brand.
  • Coordinate product recalls; communicate with customers and suppliers; submit all required documents to Health Canada.
  • File mandatory reports with Health Canada.
  • Prepare, submit, and track regulatory submissions. (incl. Summary Reports, Shortages)

Administration

  • Support and provide back-up for Quality Assurance Technician as required.
  • Maintain current body of knowledge on regulations and standards.
  • Ensure communication is effective and informative regarding issues which may affect the quality of service or products.
  • Prepare monthly and annual reports to indicate trends and summarize issues related to product complaints.
  • Ensure cooperation with special projects as required.

Skills & Qualifications

Education and Experience:

  • Post secondary diploma in Health Sciences or related discipline.
  • Post graduate certificate in Quality Assurance is an asset.
  • Documented ISO certificate/training is an asset.
  • Three (3) to five (5) years of Quality Assurance experience.

Specialized Skill Or Knowledge

  • Ability to work independently.
  • Strong interpersonal skills.
  • Excellent written and verbal communication skills.
  • Intermediate experience in Microsoft Office applications.
  • Bilingual both written and oral is an asset.

Essential Duties

  • Ability to communicate and handle quality and regulatory issues.
  • Ability to travel occasionally.
  • Ability to lift and/or move up to 50lbs (23kg).

Working Conditions

  • Office/Warehouse setting within our facility in London, ON.
  • Frequent interruptions.
  • Compensation based on a regular work week of thirty-seven and one half (37.5) working hours, with additional working hours as required to meet ongoing business demands and to full fill job responsibilities.
Since 1922, Trudell Healthcare Solutions Inc., a member of the Trudell Medical Group, has been a stable and financially sound Canadian-based employer, headquartered in London, Ontario. For over 90 years, we have enjoyed the reputation of being successful and trustworthy in the eyes of our customers, our suppliers and our staff. We are passionate about selling, servicing and distributing technologically advanced Critical Care and Respiratory products and state-of-the-art Operating Room products to hospitals across Canada.

If you feel you meet the qualifications for this role, please submit your resume with the subject line “Quality & Regulatory Coordinator – THS” to Human Resources, at hr@trudellhs.com.

We thank all applicants for their interest in joining our team. Only those to be interviewed will be contacted. For more information, visit us at www.trudellhs.com. Trudell Healthcare Solutions Inc. is an equal opportunity employer it is important to our Company that all its employees, including those with disabilities, find our workplace to be welcoming and supportive. If you are a candidate with a disability who requires accommodations during the recruitment process, please let us know.
Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Lead, Regulatory Affairs

CNIB

Calgary

Remote

CAD 48,000 - 62,000

Yesterday
Be an early applicant

Lead, Regulatory Affairs

CNIB

Toronto

Remote

CAD 48,000 - 62,000

Yesterday
Be an early applicant

Lead, Regulatory Affairs

CNIB Foundation

Vancouver

Remote

CAD 48,000 - 62,000

2 days ago
Be an early applicant

Sr Regulatory Consultant - US Strategy

Syneos Health, Inc.

Remote

USD 60,000 - 116,000

30+ days ago

Regulatory Consultant (CMC experience within LATAM or APAC region required)

Syneos Health, Inc.

Remote

CAD 60,000 - 100,000

30+ days ago