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- Tasks: Manage product registration and ensure compliance with CE and FDA regulations.
- Company: Leading medical device manufacturer in Edinburgh with a multinational team.
- Benefits: Competitive salary, personal development opportunities, and a wide array of benefits.
- Why this job: Join a dynamic team and make a difference in the medical device sector.
- Qualifications: Significant experience in medical devices and strong communication skills.
- Other info: Exciting career growth opportunities in a supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
A medical device manufacturer in Edinburgh is seeking a Senior Regulatory Affairs Officer to join their multinational team. This role involves managing product registration and ensuring compliance with CE and FDA regulations.
The ideal candidate will have:
- Significant experience in the medical device sector
- Excellent communication skills
- A strong background in regulatory roles
Competitive salary and personal development opportunities are offered, alongside a wide array of benefits.
Senior Regulatory Affairs Lead - Medical Devices (Edinburgh) employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Affairs Lead - Medical Devices (Edinburgh)
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device sector on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Senior Regulatory Affairs Lead role.
✨Tip Number 2
Prepare for interviews by brushing up on CE and FDA regulations. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and confidence when it comes to compliance.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest using our website to find roles that excite you and match your skills in regulatory affairs.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe this shows your enthusiasm for the role and keeps you fresh in their minds.
We think you need these skills to ace Senior Regulatory Affairs Lead - Medical Devices (Edinburgh)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in the medical device sector and regulatory roles. We want to see how your skills align with the requirements of the Senior Regulatory Affairs Lead position.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for our team in Edinburgh. Share specific examples of your past achievements in regulatory affairs that demonstrate your expertise.
Show Off Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Keep your language clear and concise, and don’t hesitate to showcase any relevant experiences where you’ve effectively communicated complex regulatory information.
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 shows us you’re keen on joining our multinational team!
How to prepare for a job interview at SRG
✨Know Your Regulations
Make sure you brush up on CE and FDA regulations before the interview. Being able to discuss specific compliance requirements and how they relate to the medical device sector will show that you're not just familiar with the rules, but that you can apply them effectively.
✨Showcase Your Experience
Prepare to share concrete examples from your past roles that highlight your experience in regulatory affairs. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for the interviewer to see your impact in previous positions.
✨Communicate Clearly
Since excellent communication skills are a must for this role, practice articulating complex regulatory concepts in simple terms. This will demonstrate your ability to convey important information to both technical and non-technical stakeholders.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's regulatory processes and challenges they face in the medical device industry. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
