At a Glance
- Tasks: Support lifecycle management of medical devices and ensure compliance with regulations.
- Company: Join a collaborative team at GBUK Group focused on innovative healthcare solutions.
- Benefits: Be part of a supportive environment dedicated to improving patient outcomes.
- Other info: Exciting opportunities for growth in the medical device sector.
- Why this job: Make a real impact in healthcare by ensuring safety and quality of medical devices.
- Qualifications: Background in science, engineering, or related fields with strong analytical skills.
The predicted salary is between 30000 - 40000 £ per year.
Are you passionate about medical device compliance, patient safety and bringing quality healthcare products to market? We're looking for a Regulatory & Post Market Affairs Associate to join our growing team at our North Duffield headquarters in North Yorkshire. This is an exciting opportunity to play a key role in supporting the lifecycle management of our medical devices, with responsibilities spanning:
- Post Market Surveillance (PMS) and Post Market Clinical Follow-Up (PMCF) activities
- Preparation and maintenance of PMS, PMCF and safety documentation
- Regulatory and technical file support
- Cross-functional project work with Quality, Clinical and Commercial teams
- Audit preparation and regulatory compliance activities
- Supporting innovative new product development initiatives
We're looking for someone with a scientific, medical, engineering or related background who combines strong analytical skills with exceptional attention to detail. Experience within the medical device sector is highly desirable, particularly in regulatory affairs, clinical affairs, post-market activities or quality management systems.
At GBUK Group, you'll be part of a collaborative, supportive team dedicated to improving patient outcomes through innovative medical technologies.
Interested? We'd love to hear from you. The closing date for this role is 10th June and applications must be received before that date in order to be considered. Apply now or contact us for an informal conversation about the role.
Regulatory & Post Market Affairs Associate in York employer: GBUK
At GBUK Group, we pride ourselves on being an excellent employer, offering a collaborative and supportive work culture that prioritises employee growth and development. Located in the picturesque North Duffield, North Yorkshire, our team is dedicated to improving patient outcomes through innovative medical technologies, providing opportunities for meaningful contributions in the healthcare sector. Join us to be part of a dynamic environment where your expertise in regulatory affairs can thrive, alongside a commitment to quality and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory & Post Market Affairs Associate in York
✨Tip Number 1
Network like a pro! Reach out to current employees at GBUK Group on LinkedIn or other platforms. A friendly chat can give you insider info and might just get your foot in the door.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of medical device regulations and compliance. We want to see your passion for patient safety and quality healthcare products shine through!
✨Tip Number 3
Showcase your analytical skills during the interview. Bring examples of how you've tackled complex problems in past roles, especially if they relate to regulatory affairs or post-market activities.
✨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 you’re serious about joining our team.
We think you need these skills to ace Regulatory & Post Market Affairs Associate in York
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in regulatory affairs and post-market activities. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about medical device compliance and how you can contribute to our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Attention to Detail:Given the nature of the role, attention to detail is crucial. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work!
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of being noticed. It’s quick and easy, and we can’t wait to see your application come through!
How to prepare for a job interview at GBUK
✨Know Your Stuff
Make sure you brush up on the specifics of medical device compliance and post-market activities. Familiarise yourself with relevant regulations and guidelines, as well as the company's products. This will show your genuine interest and help you answer questions confidently.
✨Showcase Your Analytical Skills
Prepare examples from your past experiences where you've demonstrated strong analytical skills and attention to detail. Think about situations where you successfully managed documentation or contributed to regulatory compliance. Be ready to discuss these in a clear and concise manner.
✨Collaborate Like a Pro
Since the role involves cross-functional project work, be prepared to talk about your experience working in teams. Highlight any collaborative projects you've been part of, especially those involving Quality, Clinical, or Commercial teams. This will demonstrate your ability to work well with others.
✨Ask Smart Questions
At the end of the interview, don’t forget to ask insightful questions about the company’s approach to post-market surveillance or their innovative product development initiatives. This shows that you're not only interested in the role but also in how you can contribute to their mission.
