At a Glance
- Tasks: Manage quality control systems and ensure compliance with industry standards.
- Company: Leading medical devices company focused 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.
Claims Quality Assurance Officer in Diss 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
✨Tip Number 1
Network like a pro! Reach out to people in the medical devices industry, especially those who work with quality assurance. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on ISO standards and quality management systems. We recommend creating a cheat sheet of key points to discuss how your experience aligns with the role's requirements.
✨Tip Number 3
Showcase your problem-solving skills! Be ready to share examples of how you've tackled quality issues in the past. This will demonstrate your ability to handle customer complaints and CAPA effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Claims Quality Assurance Officer in Diss
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 in the past and the impact of your solutions on quality outcomes.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s straightforward and ensures your application goes directly to us. Plus, you’ll find all the details you need about the role there!
How to prepare for a job interview at Wynne Consulting
✨Know Your Standards
Make sure you brush up on ISO13485 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, as this is crucial for the position.
✨Familiarise Yourself with Quality Metrics
Understand key performance indicators (KPIs) related to quality assurance. Be ready to discuss how you've used metrics to drive improvements in previous roles, as this will demonstrate your analytical skills and focus on continuous improvement.
✨Engage with Cross-Functional Teams
Think about your experience working with different teams, especially in quality engineering or continuous improvement projects. Be prepared to share how you’ve collaborated with others to enhance quality processes, as teamwork is essential in this role.