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- Tasks: Manage product licence registrations and ensure compliance with international regulations.
- Company: Leading IVD manufacturer with a focus on innovation and quality.
- Benefits: Relocation support, competitive salary, and opportunities for professional growth.
- Why this job: Join a dynamic team and make a difference in the medical device industry.
- Qualifications: Experience in the medical device industry and relevant qualifications required.
- Other info: On-site work 3 times a week in beautiful Edinburgh.
The predicted salary is between 36000 - 60000 £ per year.
A leading IVD manufacturer is seeking a Regulatory Affairs professional to manage product licence registrations and ensure compliance with international regulations. This role includes preparing regulatory documentation, advising project teams, and maintaining product labelling standards.
The ideal candidate will have experience in the medical device industry and relevant qualifications.
This position is on-site 3 times a week in the outskirts of Edinburgh, Scotland, with potential relocation support offered.
Regulatory Affairs Officer – IVD (Relocation Support) in Edinburgh employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Officer – IVD (Relocation Support) in Edinburgh
✨Tip Number 1
Network like a pro! Reach out to professionals in the IVD and medical device industry on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of international regulations and product labelling standards. We recommend practising common interview questions related to regulatory affairs to boost your confidence.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It shows professionalism and keeps you on their radar.
✨Tip Number 4
Apply through our website for the best chance at landing that Regulatory Affairs Officer position. We make it easy for you to showcase your skills and experience directly to the hiring team!
We think you need these skills to ace Regulatory Affairs Officer – IVD (Relocation Support) in Edinburgh
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, especially in the IVD or medical device industry. We want to see how your skills match the job description, so don’t be shy about showcasing relevant qualifications!
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 engaging – we love a good story!
Showcase Your Compliance Knowledge: Since this role involves ensuring compliance with international regulations, make sure to mention any specific regulations you’re familiar with. We’re looking for someone who knows their stuff, so don’t hold back!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulations
Make sure you brush up on the latest international regulations related to IVD products. Familiarise yourself with the specific compliance requirements that the company adheres to, as this will show your commitment and understanding of the role.
✨Prepare Your Documentation Examples
Since the role involves preparing regulatory documentation, come prepared with examples of your past work. Highlight any successful submissions or projects you've managed, and be ready to discuss the challenges you faced and how you overcame them.
✨Understand the Product Labelling Standards
Research the product labelling standards relevant to the IVD industry. Be prepared to discuss how you would ensure compliance in this area and any experiences you have had with maintaining or improving labelling standards in previous roles.
✨Show Your Team Spirit
This position requires advising project teams, so be ready to demonstrate your collaborative skills. Share examples of how you've worked effectively with cross-functional teams in the past, and emphasise your ability to communicate complex regulatory information clearly.
