Regulatory Affairs Associate — Medical Devices (Gloucester)
Regulatory Affairs Associate — Medical Devices (Gloucester)

Regulatory Affairs Associate — Medical Devices (Gloucester)

Gloucester Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure regulatory compliance and manage technical documentation for medical devices.
  • Company: Leading manufacturing business in Gloucester with a focus on innovation.
  • Benefits: Competitive salary, career development opportunities, and a supportive work environment.
  • Why this job: Join a vital role in the medical device industry and make a difference in healthcare.
  • Qualifications: Experience in medical device regulations and strong teamwork skills.
  • Other info: Opportunity to work in a dynamic team with potential for growth.

The predicted salary is between 30000 - 42000 £ per year.

A leading manufacturing business based in Gloucester is seeking a Regulatory Affairs Associate. In this role, you will be responsible for maintaining regulatory compliance and managing technical documentation in accordance with international standards like ISO 13485 and FDA regulations.

Ideal candidates should have experience in medical device regulations and auditing, and the ability to work across teams to ensure timely regulatory deliverables.

Interested applicants can reach out to Ben Herd for more information.

Regulatory Affairs Associate — Medical Devices (Gloucester) employer: Omega

As a leading manufacturing business in Gloucester, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to thrive. We offer competitive benefits, continuous professional development opportunities, and a commitment to maintaining the highest standards of regulatory compliance in the medical device industry, making us an excellent employer for those seeking meaningful and rewarding careers.
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Contact Detail:

Omega Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs Associate — Medical Devices (Gloucester)

Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field, especially those working with medical devices. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!

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 that showcase your knowledge. This will help you stand out when discussing your qualifications.

Tip Number 3

Don’t just apply anywhere—focus on companies that align with your values and career goals. Check out our website for openings that match your skills in regulatory affairs. Tailor your approach to each company to show you’re genuinely interested!

Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.

We think you need these skills to ace Regulatory Affairs Associate — Medical Devices (Gloucester)

Regulatory Compliance
Technical Documentation Management
ISO 13485
FDA Regulations
Medical Device Regulations
Auditing
Cross-Functional Collaboration
Timely Regulatory Deliverables

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience with medical device regulations and auditing. We want to see how your skills align 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 regulatory affairs and how you can contribute to our team. Keep it concise but impactful – we love a good story!

Showcase Teamwork Skills: Since this role involves working across teams, make sure to mention any collaborative projects you've been part of. We value teamwork, so let us know how you’ve successfully worked with others to achieve regulatory goals.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates!

How to prepare for a job interview at Omega

Know Your Regulations

Make sure you brush up on ISO 13485 and FDA regulations before the interview. Being able to discuss these standards confidently will show that you understand the core of the role and can hit the ground running.

Showcase Your Experience

Prepare specific examples from your past work where you've successfully managed regulatory compliance or technical documentation. This will help demonstrate your hands-on experience and how it aligns with what the company is looking for.

Teamwork Matters

Since the role involves working across teams, be ready to talk about your collaboration skills. Think of instances where you’ve worked with different departments to achieve a common goal, and highlight your ability to communicate effectively.

Ask Insightful Questions

Prepare thoughtful questions about the company's regulatory processes or upcoming projects. This not only shows your interest in the role but also gives you a chance to assess if the company is the right fit for you.

Regulatory Affairs Associate — Medical Devices (Gloucester)
Omega
Location: Gloucester
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  • Regulatory Affairs Associate — Medical Devices (Gloucester)

    Gloucester
    Full-Time
    30000 - 42000 £ / year (est.)
  • O

    Omega

    50-100
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