Regulatory Affairs Specialist in Watford
Regulatory Affairs Specialist

Regulatory Affairs Specialist in Watford

Watford Full-Time 40000 - 60000 ÂŁ / year (est.) No home office possible
Medtronic

At a Glance

  • Tasks: Support regulatory activities for medical devices and ensure compliance with UK and Ireland standards.
  • Company: Join Medtronic, a leader in global healthcare technology and innovation.
  • Benefits: Competitive salary, flexible benefits, and a commitment to employee success.
  • Why this job: Make a real impact on healthcare access and equity while growing your career.
  • Qualifications: Experience in medical device regulation and strong analytical skills required.
  • Other info: Dynamic work environment with opportunities for personal and professional growth.

The predicted salary is between 40000 - 60000 ÂŁ per year.

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

We are seeking an experienced Regulatory Affairs Specialist to support post-market regulatory activities for medical devices. The role includes field safety corrective actions, regulatory authority inquiries, complaint process support, and regulatory documentation requests from customers, sales teams, and internal stakeholders.

Responsibilities may include the following and other duties may be assigned:

  • Monitor and interpret regulatory requirements for the UK and Ireland, ensuring updates are implemented in compliance with regulatory standards
  • Coordinate and support Field Safety Corrective Actions (FSCAs), working with sales teams and the FCA Support Team to ensure timely completion
  • Manage and respond to inquiries from Competent Authorities, including maintaining accurate regulatory records and reporting
  • Provide guidance to sales teams on product complaint handling and returns to ensure compliance with regulations and internal procedures
  • Support product registration and “placing on the market” activities, providing country-specific regulatory guidance
  • Manage regulatory documentation requests from customers, tender teams, and internal stakeholders, ensuring accurate and timely responses
  • Coordinate requests with relevant internal teams and ensure appropriate follow-up and resolution

Required Knowledge and Experience:

  • Experience in medical device regulatory
  • Strong computer skills, including Microsoft Office (especially Excel) and the ability to work with internal systems
  • Strong analytical, problem-solving, and organizational skills
  • Ability to work independently and manage multiple tasks effectively
  • Detail-oriented with a strong focus on quality and patient safety

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Pay range: United Kingdom: 40,000.00 GBP - 60,000.00 GBP | This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

Regulatory Affairs Specialist in Watford employer: Medtronic

At Medtronic, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. Our commitment to employee growth is evident through comprehensive training programmes and a supportive environment that encourages career advancement. Located in the UK, we provide competitive salaries and a flexible benefits package, ensuring our team members feel valued and empowered to make a meaningful impact in healthcare.
Medtronic

Contact Detail:

Medtronic Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs Specialist in Watford

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.

✨Tip Number 2

Prepare for interviews by researching Medtronic's values and recent projects. Show us that you’re not just another candidate; demonstrate your passion for healthcare innovation and how you can contribute to our mission.

✨Tip Number 3

Practice your responses to common interview questions, especially those related to regulatory affairs. We want to see your analytical skills and problem-solving abilities shine through!

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us you’re genuinely interested in joining our team.

We think you need these skills to ace Regulatory Affairs Specialist in Watford

Regulatory Knowledge for Medical Devices
Field Safety Corrective Actions (FSCAs)
Regulatory Authority Inquiries
Complaint Process Support
Regulatory Documentation Management
Microsoft Office (especially Excel)
Analytical Skills
Problem-Solving Skills
Organisational Skills
Attention to Detail
Quality Focus
Patient Safety Awareness
Ability to Work Independently
Task Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Specialist role. Highlight your experience in medical device regulations and any relevant skills that match the job description. We want to see how you can bring value to our team!

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 your background aligns with our mission at Medtronic. Let us know what excites you about this opportunity!

Showcase Your Skills: Don’t forget to showcase your strong analytical, problem-solving, and organisational skills in your application. We’re looking for detail-oriented candidates who can manage multiple tasks effectively, so make sure to highlight these abilities!

Apply Through Our Website: We encourage you to apply through our website for the best chance of success. It’s the easiest way for us to review your application and get you on the path to joining our innovative team at Medtronic!

How to prepare for a job interview at Medtronic

✨Know Your Regulations

Make sure you brush up on the latest regulatory requirements for medical devices in the UK and Ireland. Familiarise yourself with any recent changes, as this will show your commitment to compliance and your understanding of the industry.

✨Showcase Your Problem-Solving Skills

Prepare examples from your past experience where you've successfully navigated regulatory challenges or managed inquiries from Competent Authorities. This will demonstrate your analytical skills and ability to handle complex situations effectively.

✨Be Detail-Oriented

During the interview, highlight your attention to detail by discussing how you ensure accuracy in regulatory documentation and compliance processes. Mention specific tools or methods you use to maintain high-quality standards.

✨Engage with the Team

Since collaboration is key in this role, be ready to discuss how you’ve worked with sales teams and internal stakeholders in the past. Show that you can coordinate effectively and follow up on tasks to ensure timely completion of projects.

Regulatory Affairs Specialist in Watford
Medtronic
Location: Watford

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