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- Tasks: Join a dynamic team ensuring top-notch quality in medical devices.
- Company: Newton Colmore is a specialist consultancy in the medical devices sector.
- Benefits: Enjoy competitive salary, career progression, and hands-on training.
- Why this job: Make a real impact on healthcare while working closely with production experts.
- Qualifications: Experience in medical devices and knowledge of ISO 13485 and ISO 14971 required.
- Other info: This is a fully onsite role with a two-stage interview process.
The predicted salary is between 28800 - 48000 £ per year.
Newton Colmore is working with a medical devices company in the West Midlands, assisting them with their search for a key Quality Engineer hire. The role as Quality Engineer will give you the opportunity to work on market leading medical devices while collaborating closely with the production team to ensure that the parts delivered from the company's suppliers meet the design specifications and quality requirements.
The quality engineer will help the production team in supplier quality assessments, including creating and following up on SCARs, and will also ensure that the Device History Record (DHR) is up to date for products manufactured. This is a key new role within the team, reporting directly to the head of the team and collaborating with the five members of the production team.
This role will also cover key responsibilities such as:
- Incoming inspection of parts
- Customer returns
- Ensuring that document control, CAPA, and the complaints process are followed effectively
To be considered for the Quality Engineer role, you will need to have prior medical devices experience, ideally with both ISO 13485 and ISO 14971 standards. This will be paired with quality control and production knowledge within a manufacturing environment.
In return for your hard work, the company offers a highly competitive salary and benefits package, as well as excellent career progression opportunities and hands-on training. Because of how closely you will be working with the production team, this will be a fully onsite role.
In regard to the process, there is a two-stage interview where you will be invited to showcase your skills and experience while finding out more about the company, their mission, and what they can offer you. To enter the recruitment process, click apply now, and if you have the right skills and expertise, I will be in touch to discuss the opportunity further.
Quality Engineer - Medical Devices in Birmingham) employer: Newton Colmore Consulting
Contact Detail:
Newton Colmore Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Engineer - Medical Devices in Birmingham)
✨Tip Number 1
Familiarise yourself with ISO 13485 and ISO 14971 standards, as these are crucial for the role. Understanding these regulations will not only help you in the interview but also demonstrate your commitment to quality in medical devices.
✨Tip Number 2
Prepare to discuss specific examples from your previous experience where you've successfully managed supplier quality assessments or handled SCARs. This will showcase your practical knowledge and problem-solving skills relevant to the position.
✨Tip Number 3
Research the company’s mission and values thoroughly. Being able to articulate how your personal values align with theirs during the interview can set you apart from other candidates.
✨Tip Number 4
Since this role involves close collaboration with the production team, think of ways to highlight your teamwork and communication skills. Prepare anecdotes that illustrate your ability to work effectively in a team environment.
We think you need these skills to ace Quality Engineer - Medical Devices in Birmingham)
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the key responsibilities and requirements for the Quality Engineer position. Highlight your relevant experience with medical devices, ISO 13485, and ISO 14971 standards in your application.
Tailor Your CV: Customise your CV to reflect your experience in quality control and production within a manufacturing environment. Use specific examples that demonstrate your skills in supplier quality assessments and document control.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention how your background aligns with the company's mission and the importance of quality in medical devices.
Prepare for the Interview: Since there is a two-stage interview process, prepare by reviewing common interview questions related to quality engineering and medical devices. Be ready to discuss your previous experiences and how they relate to the responsibilities of the role.
How to prepare for a job interview at Newton Colmore Consulting
✨Know Your Standards
Familiarise yourself with ISO 13485 and ISO 14971 standards, as these are crucial for the role. Be prepared to discuss how your previous experience aligns with these standards and how you have applied them in past projects.
✨Showcase Your Collaboration Skills
Since the role involves working closely with the production team, highlight your teamwork experiences. Share specific examples of how you've successfully collaborated with others to achieve quality goals or resolve issues.
✨Prepare for Technical Questions
Expect technical questions related to quality control processes, supplier assessments, and document control. Brush up on your knowledge of CAPA and complaint processes, and be ready to explain how you've implemented these in your previous roles.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality management systems and their approach to continuous improvement. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
