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- Tasks: Lead the creation of clinical evaluation documents and provide regulatory insights.
- Company: A top medical device company in Eastleigh with a focus on innovation.
- Benefits: Competitive pay and great opportunities for professional growth.
- Why this job: Make a real difference in healthcare by ensuring compliance with EU regulations.
- Qualifications: Extensive medical writing experience and knowledge of EU Medical Device Directive.
- Other info: Collaborative environment with cross-functional teams.
The predicted salary is between 42000 - 84000 £ per year.
A leading medical device company in Eastleigh is seeking a skilled Lead Medical Writer to supervise the creation of clinical evaluation documentation and provide crucial regulatory insights. The candidate will work closely with cross-functional teams to ensure compliance with EU regulations.
Essential qualifications include extensive experience in medical writing and a strong understanding of the EU Medical Device Directive. The position offers competitive compensation and ample opportunities for professional growth.
Senior Medical Writer: EU MDR, CER & Regulatory Expert in Eastleigh employer: CooperVision
Contact Detail:
CooperVision Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Medical Writer: EU MDR, CER & Regulatory Expert in Eastleigh
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical writing field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU regulations and the Medical Device Directive. We recommend practising common interview questions with a friend to boost your confidence and ensure you shine during the real deal.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your best work, including clinical evaluation documents and regulatory submissions. This will give potential employers a taste of what you can bring to the table.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always on the lookout for talented individuals like you to join our team.
We think you need these skills to ace Senior Medical Writer: EU MDR, CER & Regulatory Expert in Eastleigh
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in medical writing and your understanding of the EU Medical Device Directive. We want to see how your skills align with what we're looking for, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the Senior Medical Writer role. We love seeing passion and personality, so let us know what excites you about working with us and how you can contribute to our team.
Showcase Your Regulatory Knowledge: Since this role involves crucial regulatory insights, make sure to highlight any experience you have with EU regulations. We’re keen on candidates who can demonstrate their expertise in clinical evaluation documentation and compliance.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about us and what we do!
How to prepare for a job interview at CooperVision
✨Know Your Regulations
Make sure you brush up on the EU Medical Device Directive and any recent changes. Being able to discuss these regulations confidently will show that you're not just familiar with the basics, but that you’re also proactive about staying updated.
✨Showcase Your Writing Skills
Prepare samples of your previous medical writing work, especially clinical evaluation documentation. Be ready to discuss your writing process and how you ensure compliance with regulatory standards. This will demonstrate your expertise and attention to detail.
✨Collaborate Like a Pro
Since this role involves working with cross-functional teams, think of examples where you've successfully collaborated with others. Highlight your communication skills and how you’ve navigated challenges in team settings to achieve compliance goals.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to regulatory compliance and their expectations for the role. This shows your genuine interest in the position and helps you gauge if the company culture aligns with your values.
