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- Tasks: Execute regulatory activities for medical devices and support new product development.
- Company: Leading healthcare company making a difference in health for humanity.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Why this job: Join us to make a real impact in the MedTech industry.
- Qualifications: Significant regulatory experience with medical devices and a relevant degree.
- Other info: Collaborative environment with a focus on compliance and innovation.
The predicted salary is between 42000 - 60000 £ per year.
A leading healthcare company is looking for a Regulatory Affairs Senior Associate in Leeds. This hybrid role involves executing regulatory activities for marketed devices and supporting new product development. The ideal candidate must possess significant regulatory experience, especially with medical devices.
Responsibilities include:
- Coordinating CE marking and regulatory submissions globally
- Ensuring compliance with regulatory requirements
- Collaborating across functions
A relevant degree and proficiency in Microsoft Office are essential. Join us to impact health for humanity.
Senior Regulatory Affairs Lead — Orthopaedics MedTech in Leeds employer: Johnson & Johnson MedTech
Contact Detail:
Johnson & Johnson MedTech Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Affairs Lead — Orthopaedics MedTech in Leeds
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field, especially those in orthopaedics. LinkedIn is a great place to connect and engage with industry experts who can provide insights or even refer you to opportunities.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of CE marking and global regulatory submissions. We recommend creating a list of common interview questions related to regulatory affairs and practising your responses to showcase your expertise.
✨Tip Number 3
Showcase your experience with medical devices in your conversations. Be ready to discuss specific projects you've worked on and how they relate to compliance and regulatory requirements. This will help us see your hands-on experience in action!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Senior Regulatory Affairs Lead — Orthopaedics MedTech in Leeds
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your regulatory experience, especially with medical devices. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs in orthopaedics and how you can contribute to our mission. Keep it engaging and relevant!
Showcase Your Team Spirit: Collaboration is key in this role, so highlight any experiences where you’ve worked across functions. We love seeing candidates who can work well with others to achieve common goals!
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’s super easy!
How to prepare for a job interview at Johnson & Johnson MedTech
✨Know Your Regulations
Make sure you brush up on the latest regulations related to medical devices, especially CE marking. Being able to discuss specific regulatory frameworks and how they apply to the role will show that you're not just familiar with the basics but are genuinely invested in the field.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles where you've successfully navigated regulatory submissions or ensured compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your achievements.
✨Collaboration is Key
Since this role involves working across functions, be ready to discuss how you've collaborated with different teams in the past. Think of specific instances where your teamwork made a difference in achieving regulatory goals or product development.
✨Get Comfortable with Tech
Proficiency in Microsoft Office is essential, so make sure you're comfortable discussing how you've used these tools in your previous roles. Whether it's creating reports, managing data, or presenting findings, being tech-savvy will give you an edge.
