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- Tasks: Manage quality control systems and ensure compliance with industry standards.
- Company: Leading medical devices company with a focus on innovation and quality.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Great career advancement potential in a supportive environment.
- Why this job: Join a dynamic team making a real difference in healthcare quality.
- Qualifications: Experience with ISO standards and quality management in medical devices.
The predicted salary is between 40000 - 50000 £ per year.
Develops, implements and maintains the activities of quality control systems. Oversees development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products. Develops budget and monitors expenditures. Ensures all aspects of ISO13485, relevant standards and applicable regulatory requirements are met and upheld within the QMS and the Organisation.
Makes recommendations for corrective action necessary to ensure conformity with quality specifications. Ensures finished products conform to government and company standards and satisfy good manufacturing practices regulations. Selects, develops and evaluates personnel to ensure the efficient operation of the function. First level of managerial position. Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals. Works on issues of a diverse scope where analysis of situation or data requires evaluation of a variety of factors. Typically manages a department of Professional track employees but may also have support track direct or indirect reports.
Duties & Responsibilities
- Ownership & management of customer complaints investigations (CAPA) with focus on preventive actions implementation and their effectiveness verification; preparation, analysis & distribution of associated KPI metrics.
- Active participation in continuous improvement and maintenance of company’s integrated QEHSMS accredited to ISO13485/9001/14001/45001 with the emphasis on medical devices manufacturing compliance – development, review & update of relevant QEHSMS documentation; internal audits etc.
- Active participation in suppliers quality management – review & approval process; supplier audits; purchased product control plans preparation, review and approval.
- Risk management oversight: preparation of process FMEAs, manufacturing process verification & validation management.
- Participation in Optical Measuring System programming for inspections of purchased product (training provision to be given).
- Quality Engineering support as part of day-to-day business as well as part of the cross-functional teams for continuous improvement activities.
- Any other duties and responsibilities as required.
Technical Requirements
- Working Knowledge of ISO13485/9001/14001/45001 with the emphasis on medical devices manufacturing compliance – development.
- Workplace Health and Safety Legislation.
- Practical knowledge of EU MDR.
- Six Sigma.
Locations
Claims Quality Assurance Officer in Diss, Norfolk employer: Wynne Consulting
Contact Detail:
Wynne Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Claims Quality Assurance Officer in Diss, Norfolk
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. 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 researching the company and its products. Understand their quality control systems and ISO standards. This will help you show that you're not just interested in the role, but that you genuinely care about their mission.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to quality assurance and compliance. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your achievements.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive and engaged with our platform.
We think you need these skills to ace Claims Quality Assurance Officer in Diss, Norfolk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Claims Quality Assurance Officer role. Highlight your experience with ISO standards and quality management systems, as these are key for us. Use specific examples that showcase your skills in quality control and compliance.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Tell us why you're passionate about quality assurance in medical devices. Mention any relevant projects or achievements that demonstrate your expertise and how you can contribute to our team.
Showcase Your Analytical Skills: Since the role involves evaluating data and making recommendations, be sure to highlight your analytical skills. Share examples of how you've tackled complex problems or improved processes in previous roles. We love a good problem-solver!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy!
How to prepare for a job interview at Wynne Consulting
✨Know Your Standards
Make sure you brush up on ISO13485, ISO9001, and other relevant standards before the interview. Being able to discuss how these standards apply to quality management in medical devices will show that you're serious about the role.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've handled customer complaints or CAPA investigations in the past. Highlight your approach to implementing preventive actions and verifying their effectiveness—this is key for the role!
✨Familiarise Yourself with Risk Management
Understand the basics of FMEAs and how they relate to manufacturing processes. Be ready to discuss any experience you have with risk management oversight, as this will be a significant part of the job.
✨Engage with Continuous Improvement
Think of specific instances where you've contributed to continuous improvement initiatives. Whether it's through internal audits or supplier quality management, showing your proactive attitude will impress the interviewers.