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- Tasks: Oversee production quality and ensure compliance with industry standards in medical device manufacturing.
- Company: Leading medical device manufacturer focused on quality and innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real difference in healthcare by ensuring top-notch product quality.
- Qualifications: Experience in quality assurance and knowledge of ISO standards required.
- Other info: Join a dynamic team dedicated to continuous improvement and excellence.
The predicted salary is between 36000 - 60000 £ per year.
Responsible for all aspects of production quality including the quality management system. Ensuring compliance to customer, industry, and regulatory requirements, including ISO. Administer any day-to-day issues, including customer queries and assist in the implementation of a robust supplier documentation pack, specifications and analysis.
- Influence active participation at all levels, from strategy through to implementation, motivating all staff to ensure commitment to the overall business systems.
- Maintain monthly Quality Communication Strategy for all sites and staff, to include written information, toolbox talks and management briefs.
- Complete weekly certificates of conformity and produce regular and ad hoc quality reports as required.
- Ensure the company maintains all accreditations including ISO, plan and conduct internal audits, and continually develop the manual and procedures.
- Review current quality testing procedures and specifications and create and implement new quality testing procedures to streamline current testing practices to ensure we are producing material that always meets customer specifications.
- Understand and support with PRN applications and calculations.
- Liaise with BDMs and ensure dock testing of raw stock, ensure findings are recorded and communicated where required.
- Ensure compliance with end of waste (EOW) regulations for glass cullet including tests, standard updates and reporting.
- Maintain process flow diagrams for each plant.
- SOP management, amendments, update and additions where required.
- Investigate the root cause of any external customer complaint (NCRs), record the complaint in line with company procedure and include the implementation of corrective and preventative actions, feed back to the business where required.
- Develop new standards for production, with improvements as needed, and create testing protocols and plans for implementation across all sites.
- Take ownership of the Purgo quality data and produce weekly reports on the trends and statistics, which will help to improve quality and prevent failures.
- Maintain complaint and nonconformance processing through records and tracking systems, including root cause and corrective actions.
- Involvement with site PPM schedule and daily maintenance plan to ensure any tasks which will impact quality is controlled.
Strong knowledge of waste classification technical guidance WM3. Previous experience within quality assurance. Experience of implementing and maintaining ISO and end of Waste. Risk management experience. Evaluate process risk and implement actions to prevent incidents. Ability to deliver training and influence all employees at all levels business in all aspects of quality. Experience of manufacturing techniques including Six Sigma, 5S, Lean. Excellent communication skills both verbal & in writing. People Management.
Quality Manager-Medical Device Manufacturing in Pontefract employer: Arthur Rose Recruitment
Contact Detail:
Arthur Rose Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Manager-Medical Device Manufacturing in Pontefract
✨Tip Number 1
Network like a pro! Get out there and connect with people in the medical device manufacturing industry. Attend events, join relevant groups on LinkedIn, and don’t be shy about reaching out to potential employers directly. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by researching the company’s quality management systems and recent projects. Show them you’re not just another candidate; you’re genuinely interested in their work and how you can contribute to maintaining those ISO standards they value so much.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to quality assurance and compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience with ISO and risk management.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly shows your enthusiasm. Plus, it makes it easier for us to keep track of your application and get back to you quickly!
We think you need these skills to ace Quality Manager-Medical Device Manufacturing in Pontefract
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Manager role. Highlight your experience with ISO standards, quality management systems, and any relevant manufacturing techniques like Six Sigma or Lean. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in medical device manufacturing. Share specific examples of how you've influenced quality improvements in previous roles. We love a good story!
Show Off Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and concise language, and don’t shy away from showcasing your ability to communicate complex quality concepts effectively. We appreciate clarity!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Arthur Rose Recruitment
✨Know Your Quality Standards
Make sure you brush up on ISO standards and any relevant regulations before the interview. Being able to discuss how you've implemented or maintained these standards in previous roles will show your expertise and commitment to quality management.
✨Prepare for Scenario Questions
Expect questions that ask you to describe how you've handled specific quality issues or customer complaints in the past. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Show Your Leadership Skills
As a Quality Manager, you'll need to influence and motivate staff at all levels. Be ready to share examples of how you've successfully led teams or driven quality initiatives in previous positions. Highlight your communication skills and ability to train others.
✨Bring Data to the Table
Since the role involves analysing quality data and producing reports, come prepared with examples of how you've used data to improve processes or resolve issues. Discuss any tools or methodologies you've employed, like Six Sigma or Lean, to demonstrate your analytical skills.
