Graduate Regulatory Engineer
Graduate Regulatory Engineer

Graduate Regulatory Engineer

Basildon Entry level 28800 - 48000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Assist in regulatory documentation and ensure compliance for medical devices.
  • Company: Join an innovative leader in the medical technology industry.
  • Benefits: Enjoy comprehensive training, mentorship, and a supportive team environment.
  • Why this job: Make a real impact in healthcare while working on life-changing products.
  • Qualifications: Degree in Biomedical or Mechanical Engineering; strong attention to detail required.
  • Other info: On-site role in Chelmsford with relocation allowance available.

The predicted salary is between 28800 - 48000 £ per year.

Must hold full right to work, no sponsorship available.

On-site 5 days/week in Chelmsford - Relocation allowance available.

Are you a recent graduate looking to start your career in the exciting world of medical devices? My client, an innovative leader in the medical technology industry, is seeking a Graduate Regulatory Engineer to join their growing team. This is a fantastic opportunity to gain hands-on experience in a highly regulated and rewarding sector while contributing to life-changing healthcare solutions.

About the Role:

As a Graduate Regulatory Engineer, you’ll play a key role in ensuring compliance with global regulatory standards while supporting the development of cutting-edge medical devices. You’ll work closely with experienced professionals and cross-functional teams to bring innovative products to market safely and efficiently.

Key Responsibilities:

  • Assist in preparing and submitting regulatory documentation for global approvals (e.g., 510(k), CE marking).
  • Support the development and maintenance of Quality Management Systems (QMS) compliant with ISO 13485 and FDA regulations.
  • Contribute to risk management activities, including dFMEA and pFMEA processes.
  • Review and maintain documentation to ensure regulatory and quality standards are met throughout the product lifecycle.
  • Collaborate with R&D, quality assurance, and manufacturing teams on compliance and process improvements.

What We’re Looking For:

  • A degree in Biomedical Engineering, Mechanical Engineering, or a related discipline.
  • Strong attention to detail and excellent problem-solving skills.
  • An interest in regulatory frameworks and quality assurance within the medical device industry.
  • Strong communication skills and a collaborative attitude.
  • Prior internship or project experience in the medical device sector is advantageous but not required.

What’s on Offer:

  • Comprehensive training and mentorship to develop your regulatory expertise.
  • A supportive, collaborative team environment.
  • The chance to work on innovative products that improve patient outcomes.
  • A clear pathway for career growth within the medical device industry.

This is an incredible opportunity to launch your career with a company that values innovation, quality, and improving lives. If you’re interested, please apply or get in touch with me directly for more details. Don’t miss this chance to join a pioneering organization and make a real impact in healthcare!

Graduate Regulatory Engineer employer: Arevna

Join a pioneering leader in the medical technology industry as a Graduate Regulatory Engineer in Chelmsford, where you'll benefit from comprehensive training and mentorship in a supportive, collaborative environment. This role offers a unique opportunity to work on innovative medical devices that enhance patient outcomes, with a clear pathway for career growth in a sector dedicated to improving lives. Relocation assistance is available, making it an ideal choice for recent graduates eager to make a meaningful impact in healthcare.
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Contact Detail:

Arevna Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Graduate Regulatory Engineer

✨Tip Number 1

Familiarise yourself with the key regulatory frameworks relevant to medical devices, such as ISO 13485 and FDA regulations. Understanding these standards will not only help you in interviews but also demonstrate your genuine interest in the role.

✨Tip Number 2

Network with professionals in the medical device industry through platforms like LinkedIn. Engaging with current employees or joining relevant groups can provide insights into the company culture and the specific skills they value.

✨Tip Number 3

Consider reaching out to alumni from your university who are working in regulatory roles within the medical device sector. They can offer valuable advice on how to navigate your career path and may even refer you to open positions.

✨Tip Number 4

Stay updated on the latest trends and innovations in medical technology. Being knowledgeable about recent advancements can set you apart during discussions and show your enthusiasm for the field.

We think you need these skills to ace Graduate Regulatory Engineer

Attention to Detail
Problem-Solving Skills
Understanding of Regulatory Frameworks
Knowledge of Quality Management Systems (QMS)
Familiarity with ISO 13485
Familiarity with FDA Regulations
Risk Management Skills
Experience with dFMEA and pFMEA processes
Strong Communication Skills
Collaborative Attitude
Analytical Skills
Project Management Skills
Ability to Work in Cross-Functional Teams
Adaptability to a Fast-Paced Environment

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant coursework, projects, or internships related to Biomedical or Mechanical Engineering. Emphasise any experience with regulatory frameworks or quality assurance in the medical device sector.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the medical device industry and your eagerness to learn. Mention specific skills that align with the job description, such as attention to detail and problem-solving abilities.

Highlight Relevant Skills: In your application, clearly outline your skills that match the job requirements, such as communication, collaboration, and any familiarity with ISO 13485 or FDA regulations. Use examples to demonstrate these skills.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in regulatory engineering.

How to prepare for a job interview at Arevna

✨Understand Regulatory Frameworks

Familiarise yourself with key regulatory frameworks relevant to medical devices, such as ISO 13485 and FDA regulations. Being able to discuss these during your interview will demonstrate your genuine interest in the field and show that you are proactive in your learning.

✨Showcase Problem-Solving Skills

Prepare examples from your academic projects or internships where you faced challenges and how you resolved them. Highlighting your problem-solving skills will be crucial, especially since the role involves risk management activities like dFMEA and pFMEA.

✨Emphasise Team Collaboration

Since the role requires working closely with cross-functional teams, be ready to discuss your experiences in collaborative settings. Share specific instances where you contributed to a team project, showcasing your communication skills and collaborative attitude.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s approach to regulatory compliance and product development. This not only shows your enthusiasm for the role but also helps you gauge if the company culture aligns with your career aspirations.

Graduate Regulatory Engineer
Arevna
A
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