Regulatory & QA Associate, Medical Devices – Cambridge
Regulatory & QA Associate, Medical Devices – Cambridge

Regulatory & QA Associate, Medical Devices – Cambridge

Cambridge Full-Time 30000 - 40000 £ / year (est.) No home office possible
Newton Colmore Consulting Ltd

At a Glance

  • Tasks: Support regulatory and quality assurance efforts in the medical devices sector.
  • Company: Leading medical devices company based in Cambridge with a focus on innovation.
  • Benefits: Attractive salary, career progression, and opportunities for professional growth.
  • Other info: Exciting environment with potential for significant career advancement.
  • Why this job: Join a dynamic team and contribute to impactful medical innovations.
  • Qualifications: Relevant degree and experience in regulatory affairs or quality assurance.

The predicted salary is between 30000 - 40000 £ per year.

A medical devices company in Cambridge seeks a Regulatory Affairs and Quality Assurance Assistant to support the Quality Assurance and Regulatory Affairs Manager. The role requires knowledge of ISO 13485 and FDA 510k, and involvement in R&D efforts. Ideal candidates will hold a relevant degree and have experience in regulatory affairs or quality assurance. The company offers excellent salary and career progression opportunities.

Regulatory & QA Associate, Medical Devices – Cambridge employer: Newton Colmore Consulting Ltd

As a leading medical devices company based in Cambridge, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to thrive. With a strong commitment to professional development, we offer exceptional career progression opportunities alongside competitive salaries, making us an ideal employer for those seeking meaningful and rewarding roles in the regulatory and quality assurance fields.
Newton Colmore Consulting Ltd

Contact Detail:

Newton Colmore Consulting Ltd Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory & QA Associate, Medical Devices – Cambridge

Tip Number 1

Network like a pro! Reach out to professionals in the medical devices field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and show your interest in regulatory affairs and quality assurance.

Tip Number 2

Prepare for interviews by brushing up on ISO 13485 and FDA 510k regulations. We recommend creating a cheat sheet with key points and examples of how you've applied these standards in past experiences. This will help you stand out during the interview!

Tip Number 3

Don’t just apply; follow up! After submitting your application through our website, send a polite email to express your enthusiasm for the role. It shows initiative and keeps you on their radar.

Tip Number 4

Showcase your R&D involvement! If you've worked on projects related to medical devices, be sure to highlight this experience in interviews. We want to see how you can contribute to the company's growth and innovation.

We think you need these skills to ace Regulatory & QA Associate, Medical Devices – Cambridge

ISO 13485
FDA 510k
Regulatory Affairs
Quality Assurance
R&D Knowledge
Relevant Degree
Experience in Regulatory Affairs
Experience in Quality Assurance

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience with ISO 13485 and FDA 510k. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or roles you've had in regulatory affairs or quality assurance.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about medical devices and how your skills can support our Quality Assurance and Regulatory Affairs Manager. Keep it concise but impactful!

Showcase Your R&D Involvement: If you’ve been involved in any R&D efforts, make sure to mention them! We love candidates who can bridge the gap between quality assurance and research, so highlight any relevant experiences that demonstrate this.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!

How to prepare for a job interview at Newton Colmore Consulting Ltd

Know Your Standards

Make sure you brush up on ISO 13485 and FDA 510k regulations before the interview. Being able to discuss these standards confidently will show that you’re serious about the role and understand the industry.

Showcase Relevant Experience

Prepare specific examples from your past experience in regulatory affairs or quality assurance. Highlight any projects where you contributed to compliance or quality improvements, as this will demonstrate your hands-on knowledge.

Research the Company

Take some time to learn about the company’s products and their R&D efforts. This will not only help you answer questions more effectively but also allow you to ask insightful questions, showing your genuine interest in the role.

Ask About Career Progression

Since the company offers excellent career progression opportunities, don’t hesitate to ask about potential growth paths during the interview. This shows that you’re thinking long-term and are eager to develop within the organisation.

Regulatory & QA Associate, Medical Devices – Cambridge
Newton Colmore Consulting Ltd
Location: Cambridge

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

>