Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington
Product Quality Engineer – Medical Devices & Regulatory QA

Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington

Kidlington Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure product quality and compliance in innovative medical imaging technology.
  • Company: A growing company in Kidlington focused on cutting-edge medical devices.
  • Benefits: Exciting career in a dynamic field with opportunities for growth.
  • Why this job: Make a real difference in healthcare through quality assurance and regulatory compliance.
  • Qualifications: Degree in Science or Engineering; experience with ISO 13485 and FDA regulations.
  • Other info: Collaborative environment with a focus on innovation and teamwork.

The predicted salary is between 36000 - 60000 £ per year.

A growing medical imaging company in Kidlington is seeking a Product Quality Engineer to oversee quality assurance and regulatory compliance. The ideal candidate will have a degree in Science or Engineering and experience with ISO 13485 and FDA regulations.

Responsibilities include:

  • Managing quality control activities
  • Supporting documentation
  • Collaborating with various teams to ensure product quality and compliance

This role offers an exciting opportunity to contribute to innovative 3D imaging technology.

Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington employer: CT19

Join a dynamic and innovative medical imaging company in Kidlington, where we prioritise quality and compliance in our cutting-edge 3D imaging technology. Our collaborative work culture fosters professional growth, offering employees opportunities to enhance their skills while contributing to meaningful advancements in healthcare. With a commitment to employee well-being and development, we provide a supportive environment that values your contributions and encourages you to thrive.
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Contact Detail:

CT19 Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington

Tip Number 1

Network like a pro! Reach out to professionals in the medical devices field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Product Quality Engineer role.

Tip Number 2

Prepare for interviews by brushing up on ISO 13485 and FDA regulations. We recommend creating a cheat sheet of key points and examples from your experience to showcase your expertise during the interview.

Tip Number 3

Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on the radar of hiring managers.

Tip Number 4

Showcase your problem-solving skills! Be ready to discuss specific challenges you've faced in quality control and how you tackled them. We want to see your critical thinking in action!

We think you need these skills to ace Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington

Quality Assurance
Regulatory Compliance
ISO 13485
FDA Regulations
Quality Control
Documentation Management
Collaboration Skills
Scientific Knowledge
Engineering Principles
Attention to Detail
Problem-Solving Skills
Communication Skills
Project Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience with ISO 13485 and FDA regulations. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!

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 devices and how you can contribute to our innovative 3D imaging technology. Keep it engaging and personal!

Showcase Team Collaboration: Since this role involves working with various teams, highlight any past experiences where you’ve successfully collaborated with others. We love seeing candidates who can work well in a team environment, so share those stories!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!

How to prepare for a job interview at CT19

Know Your Standards

Familiarise yourself with ISO 13485 and FDA regulations before the interview. Being able to discuss these standards confidently will show that you understand the importance of quality assurance in medical devices.

Showcase Your Experience

Prepare specific examples from your past work where you've successfully managed quality control activities. Highlight any collaborative projects with teams that improved product quality or compliance, as this will demonstrate your hands-on experience.

Ask Insightful Questions

Think of questions that show your interest in the company’s innovative 3D imaging technology. Inquire about their current challenges in quality assurance or how they integrate regulatory compliance into their product development process.

Demonstrate Problem-Solving Skills

Be ready to discuss how you approach problem-solving in quality assurance scenarios. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it clear how you can contribute to maintaining high standards.

Product Quality Engineer – Medical Devices & Regulatory QA in Kidlington
CT19
Location: Kidlington

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