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- Tasks: Ensure product quality by managing complaints and conducting technical investigations.
- Company: Join a growing medical devices company with a meaningful mission.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: Be part of an innovative team dedicated to continuous improvement.
- Why this job: Make a real difference in healthcare by improving product quality and compliance.
- Qualifications: 2-3 years experience in Quality or Complaint Handling, with knowledge of ISO 13485 and FDA regulations.
The predicted salary is between 35000 - 45000 £ per year.
Supports the Quality function by maintaining compliance and providing technical input to strengthen product and service quality.
The Quality Control Officer will:
- Coordinate and manage the complaint handling process for this Medical Devices company, ensuring thorough investigation, timely resolution, and accurate documentation in line with regulatory requirements.
- Conduct technical investigations into complaints, coordinating with Engineering, Production, and Service teams to establish root cause and implement corrective/preventive actions.
- Contribute to continuous improvement of the Quality Management System (QMS).
- Provide technical feedback to support product improvements and risk assessments.
- Maintain and update the complaints database, preparing reports for management review and highlighting trends or recurring issues.
The person:
- Strong knowledge of ISO 13485, FDA 21 CFR 820, and MDR requirements.
- Minimum of 2-3 years experience in a Quality or Complaint Handling role within a technical or medical device environment.
Quality Officer in Huddersfield employer: Pratap Partnership
Contact Detail:
Pratap Partnership Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Officer in Huddersfield
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical devices industry and let them know you're on the hunt for a Quality Officer role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on ISO 13485, FDA 21 CFR 820, and MDR requirements. We want you to be able to showcase your knowledge and experience confidently, so practice answering common interview questions related to quality control and complaint handling.
✨Tip Number 3
Don’t forget to highlight your problem-solving skills! When discussing your past experiences, focus on specific examples where you successfully managed complaints or implemented corrective actions. This will show potential employers that you’re the right fit for their team.
✨Tip Number 4
Apply through our website! We’ve got a range of exciting opportunities waiting for you, and applying directly can give you an edge. Plus, it’s super easy to navigate and keeps everything in one place for us to review your application quickly.
We think you need these skills to ace Quality Officer in Huddersfield
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience with ISO 13485, FDA 21 CFR 820, and MDR. We want to see how your background aligns with the Quality Control Officer role, so don’t be shy about showcasing your skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality control in the medical devices sector. We love seeing genuine enthusiasm, so let your personality come through!
Showcase Your Problem-Solving Skills: In your application, give examples of how you've tackled complaints or quality issues in the past. We’re looking for candidates who can demonstrate their ability to investigate and resolve problems effectively.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Don’t miss out!
How to prepare for a job interview at Pratap Partnership
✨Know Your Standards
Make sure you brush up on ISO 13485, FDA 21 CFR 820, and MDR requirements. Being able to discuss these standards confidently will show that you’re not just familiar with them, but that you understand their importance in the quality control process.
✨Prepare for Technical Questions
Expect questions about your experience with complaint handling and technical investigations. Think of specific examples from your past roles where you successfully resolved issues or improved processes, as this will demonstrate your hands-on experience.
✨Show Your Problem-Solving Skills
Be ready to discuss how you approach root cause analysis and corrective actions. Companies love candidates who can think critically and provide solutions, so prepare a few scenarios where you’ve made a significant impact on quality management.
✨Highlight Your Teamwork Experience
Since the role involves coordinating with various teams, be prepared to talk about your collaboration skills. Share examples of how you’ve worked with engineering, production, or service teams to enhance product quality and resolve complaints effectively.