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- Tasks: Manage regulatory change assessments for US and EU medical devices.
- Company: Life sciences consultancy in Bedford with a focus on innovation.
- Benefits: Hybrid work model, competitive salary, and professional development opportunities.
- Why this job: Join a dynamic team and make a difference in the medical device sector.
- Qualifications: Bachelor's degree and 3+ years of experience in medical devices.
- Other info: Strong communication skills and knowledge of regulatory submissions are essential.
The predicted salary is between 36000 - 60000 £ per year.
A life sciences consultancy in Bedford is seeking a Regulatory Affairs Specialist to manage change assessments for US and EU medical devices. The ideal candidate will possess a Bachelor's degree and at least 3 years of experience in the medical device sector. Strong communication skills and knowledge of regulatory submissions are essential. This role offers a hybrid work model, allowing for both office and remote work.
Global Regulatory Affairs Specialist, Medical Devices in Bedford employer: Cedent Consulting
Contact Detail:
Cedent Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Regulatory Affairs Specialist, Medical Devices in Bedford
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device sector 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 regulatory submissions. We recommend practising common interview questions related to change assessments and being ready to discuss your past experiences in detail.
✨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 Global Regulatory Affairs Specialist role. 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 Global Regulatory Affairs Specialist, Medical Devices in Bedford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in the medical device sector. We want to see how your skills align with the role, so don’t be shy about showcasing relevant projects or 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 and how your background makes you the perfect fit for our team. Keep it engaging and personal!
Show Off Your Communication Skills: Since strong communication skills are essential for this role, make sure your application reflects that. Use clear and concise language, and don’t forget to proofread for any typos or errors!
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 Cedent Consulting
✨Know Your Regulations
Make sure you brush up on the latest US and EU regulations regarding medical devices. Familiarise yourself with key regulatory submissions and change assessments, as this will show your expertise and readiness for the role.
✨Showcase Your Experience
Prepare to discuss specific examples from your past roles that highlight your experience in regulatory affairs. Think about challenges you've faced and how you overcame them, especially in the medical device sector.
✨Communicate Clearly
Strong communication skills are a must for this position. Practice articulating complex regulatory concepts in simple terms, as you may need to explain these to non-experts during the interview.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to regulatory affairs and their hybrid work model. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
