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- Tasks: Lead the creation of clinical evaluation documents and provide regulatory insights.
- Company: Top medical device company in Eastleigh with a focus on innovation.
- Benefits: Competitive salary, comprehensive benefits, and professional growth opportunities.
- Why this job: Make a real impact in the medical field while ensuring compliance with EU regulations.
- Qualifications: Extensive experience in medical writing and knowledge of EU Medical Device Directive.
- Other info: Collaborative environment with cross-functional teams for dynamic career development.
The predicted salary is between 36000 - 60000 £ per year.
A leading medical device company in Eastleigh is looking for a Lead Medical Writer to oversee the creation of clinical evaluation documentation and provide regulatory insights. You will collaborate with cross-functional teams to ensure compliance with EU regulations.
The ideal candidate has extensive experience in medical writing and understands the EU Medical Device Directive. The role offers a competitive salary and a comprehensive benefits package, along with opportunities for professional growth.
Lead 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 Lead 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 Lead Medical Writer role.
✨Tip Number 2
Prepare for interviews by brushing up on EU MDR and CER regulations. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and confidence when chatting with potential employers.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your skills and aspirations in the medical device sector.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Lead 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 the role, so don’t be shy about showcasing relevant projects!
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 Lead Medical Writer position. Share specific examples of your work and how you’ve collaborated with cross-functional teams in the past.
Showcase Your Regulatory Knowledge: Since this role involves providing regulatory insights, make sure to mention any relevant certifications or training you have. We’re looking for someone who knows their stuff when it comes to EU regulations, so let that expertise shine through!
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 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 CooperVision
✨Know Your Regulations
Make sure you brush up on the EU Medical Device Directive and any relevant regulations. Being able to discuss these confidently will show that you’re not just familiar with the rules, but that you can apply them in your writing.
✨Showcase Your Writing Skills
Prepare samples of your previous medical writing work, especially clinical evaluation documents. Be ready to discuss your writing process and how you ensure clarity and compliance in your documentation.
✨Collaborative Mindset
Since this role involves working with cross-functional teams, think of examples where you successfully collaborated with others. Highlight your communication skills and how you’ve navigated differing opinions to achieve a common goal.
✨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 and helps you gauge if the company is the right fit for you.
