At a Glance
- Tasks: Ensure quality of medical devices by collaborating with the production team and managing supplier assessments.
- Company: Join a leading medical technology company focused on innovation and quality in healthcare.
- Benefits: Enjoy competitive salary, career progression, hands-on training, and a supportive work environment.
- Other info: Two-stage interview process to showcase your skills and learn about the company's mission.
- Why this job: Be part of a mission-driven team making a real impact in the medical field.
- Qualifications: Experience in quality engineering, especially in medical technology, with strong document control skills required.
The predicted salary is between 36000 - 60000 £ per year.
Production Quality Engineer – Medical Devices
Newton Colmore is working with a medical technology company near Lichfield, and we are assisting them with their search for a key quality hire to work closely with their production team.
The role as an experienced quality engineer will give you the opportunity to work on market leading medical devices whilst working 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, and you will be 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, and ensuring that document control, CAPA, and the complaints process is followed effectively.
The company is looking for an experienced quality engineer with medical technology knowledge, mixed with strong document control and inspection testing skills.
In return for your hard work the company offer a competitive salary and benefits package as well providing excellent career progression opportunities and hands on training.
In regard to the process, there is a two-stage interview process 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.
Newton Colmore Consulting is a highly specialist recruitment consultancy operating within the medical devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors throughout Europe and the US.
Keywords: Medical Devices, Quality Engineer, Quality Control, ISO 13485, QMS, Project Engineer, ISO 14971
#J-18808-LjbffrProduction Quality Engineer – Medical Devices employer: Newton Colmore Consulting Ltd
Newton Colmore is an exceptional employer, offering a dynamic work environment in the heart of Lichfield, where you can contribute to the development of market-leading medical devices. With a strong focus on employee growth, the company provides hands-on training and clear career progression opportunities, ensuring that your skills are continuously developed while working alongside a dedicated production team committed to quality excellence.
Contact Details:
Newton Colmore Consulting Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Production Quality Engineer – Medical Devices
✨Tip Number 1
Familiarise yourself with ISO 13485 and ISO 14971 standards, as these are crucial in the medical devices sector. Understanding these regulations will not only help you during interviews but also demonstrate your commitment to quality management systems.
✨Tip Number 2
Network with professionals in the medical technology field, especially those who work in quality engineering. Attend industry events or join relevant online forums to gain insights and potentially get referrals that could lead to job opportunities.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled supplier quality assessments and document control in your previous roles. Being able to articulate your experience with SCARs and CAPA processes will set you apart from other candidates.
✨Tip Number 4
Research the company’s mission and values thoroughly before your interview. Tailoring your responses to align with their goals will show that you're genuinely interested in contributing to their success and can help you make a strong impression.
We think you need these skills to ace Production Quality Engineer – Medical Devices
Some tips for your application 🫡
Understand the Role:Read the job description thoroughly to understand the key responsibilities and required skills for the Production Quality Engineer position. Tailor your application to highlight your relevant experience in medical technology and quality engineering.
Highlight Relevant Experience:In your CV and cover letter, emphasise your experience with document control, inspection testing, and supplier quality assessments. Use specific examples that demonstrate your ability to meet design specifications and quality requirements.
Showcase Your Skills:Make sure to mention any familiarity with ISO 13485 and QMS in your application. Discuss how your skills align with the company's needs, particularly in areas like CAPA and complaints processes.
Craft a Compelling Cover Letter:Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention why you are interested in working with medical devices and how you can contribute to their mission.
How to prepare for a job interview at Newton Colmore Consulting Ltd
✨Know Your Quality Standards
Familiarise yourself with ISO 13485 and ISO 14971, as these are crucial in the medical devices sector. Be prepared to discuss how you have applied these standards in your previous roles.
✨Showcase Your Inspection Skills
Be ready to provide examples of your experience with incoming inspections and document control. Highlight specific instances where your attention to detail made a significant impact on product quality.
✨Understand the Role of CAPA
Demonstrate your knowledge of Corrective and Preventive Actions (CAPA) and how they relate to quality assurance. Prepare to discuss any relevant experiences where you successfully implemented CAPA processes.
✨Engage with the Production Team's Needs
Express your willingness to collaborate closely with the production team. Share examples of how you've worked effectively with cross-functional teams to resolve quality issues and improve processes.
