At a Glance
- Tasks: Join us as a Quality & Regulatory Coordinator, ensuring compliance and improving healthcare quality.
- Company: Trudell Healthcare Solutions has been a trusted name in healthcare for over 90 years.
- Benefits: Enjoy 3 weeks paid vacation, health benefits, and opportunities for professional development.
- Why this job: Make a real impact on patient care while working in a supportive and innovative environment.
- Qualifications: Post-secondary diploma in Health Sciences; Quality Assurance experience preferred.
- Other info: We value diversity and are committed to creating an inclusive workplace.
The predicted salary is between 36000 - 60000 £ per year.
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:
- 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. 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. 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.
- 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.
- Administration: Support and provide back-up for Quality Assurance Technician as required. Maintain current body of knowledge on regulations and standards. Prepare monthly and annual reports to indicate trends and summarize issues related to product complaints.
Skills & Qualifications:
- 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.
- 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 fulfil job responsibilities.
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.
Quality & Regulatory Coordinator employer: Trudell Healthcare Solutions
Contact Detail:
Trudell Healthcare Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality & Regulatory Coordinator
✨Tip Number 1
Familiarise yourself with ISO 13485 standards, as this is crucial for the Quality & Regulatory Coordinator role. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to quality management.
✨Tip Number 2
Network with professionals in the healthcare and quality assurance sectors. Attend industry events or join relevant online forums to connect with others who can provide insights or even refer you to opportunities at Trudell Healthcare Solutions.
✨Tip Number 3
Stay updated on current trends and changes in healthcare regulations, especially those related to medical devices. This knowledge will be beneficial during discussions and will show your proactive approach to staying informed.
✨Tip Number 4
Prepare to discuss specific examples of how you've handled quality assurance issues in the past. Being able to articulate your problem-solving skills and attention to detail will set you apart from other candidates.
We think you need these skills to ace Quality & Regulatory Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in Quality Assurance and Regulatory Compliance. Use keywords from the job description to demonstrate that you meet the qualifications and skills required for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the healthcare industry and your attention to detail. Mention specific experiences that align with the responsibilities of the Quality & Regulatory Coordinator position, such as handling product complaints or conducting audits.
Highlight Relevant Skills: In your application, emphasise your strong interpersonal skills, ability to work independently, and proficiency in Microsoft Office applications. If you have bilingual abilities, make sure to mention them as they are considered an asset.
Follow Application Instructions: Ensure you submit your application with the correct subject line 'Quality & Regulatory Coordinator – THS' as specified in the job posting. This shows attention to detail and helps your application get noticed.
How to prepare for a job interview at Trudell Healthcare Solutions
✨Show Your Passion for Quality
Make sure to express your genuine interest in quality assurance and how it impacts patient care. Share any relevant experiences that highlight your commitment to maintaining high standards.
✨Demonstrate Organisational Skills
Prepare examples of how you've successfully managed multiple tasks or projects in the past. Discuss your methods for staying organised, especially when handling documentation and compliance.
✨Be Ready for Technical Questions
Brush up on your knowledge of ISO 13485 and other relevant regulations. Be prepared to discuss how you would approach regulatory submissions and audits, showcasing your technical inclination.
✨Highlight Problem-Solving Abilities
Think of specific instances where you've had to think outside the box to resolve issues. Share these stories during the interview to demonstrate your critical thinking and problem-solving skills.