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- Tasks: Join us as a Regulatory Affairs Specialist, shaping strategies for innovative medical products.
- Company: Be part of a global leader in quality medical solutions, making a real impact on healthcare.
- Benefits: Enjoy flexible working options and a supportive team environment with growth opportunities.
- Why this job: Contribute to meaningful projects while developing your skills in a dynamic and collaborative culture.
- Qualifications: Bring at least three years of experience in Medical Devices Regulatory Affairs and strong Microsoft Office skills.
- Other info: Ideal candidates will have project management skills and a solid understanding of Quality Management Systems.
The predicted salary is between 36000 - 60000 £ per year.
An exciting Regulatory Affairs Specialist position working for a global leader in the provision of quality medical products.
- Create and contribute to regulatory strategies for new products and design changes to existing products.
- Support the maintenance of Risk Management files.
- Act as RA reviewer/approver for product labelling, packaging artwork, and marketing materials.
- Assist in the interpretation of standard, regulatory and customer requirements for implementation in the QMS.
- Provide and present data for reports and presentations.
- Provide training and support to other team members/colleagues as required.
Minimum of three years experience in Medical Devices Regulatory Affairs.
Excellent working knowledge of Microsoft Office (including Word, Excel, and OneDrive).
A practical understanding of Quality Management Systems is desirable.
Project management skills are desirable.
Regulatory Specialist and Senior Specialist employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Specialist and Senior Specialist
✨Tip Number 1
Familiarise yourself with the latest regulations and standards in the medical devices sector. This will not only help you understand the role better but also demonstrate your commitment and knowledge during interviews.
✨Tip Number 2
Network with professionals in the Regulatory Affairs field, especially those who work with medical devices. Attend industry conferences or webinars to make connections and learn about potential job openings.
✨Tip Number 3
Brush up on your project management skills, as they are desirable for this role. Consider taking a short course or certification that can enhance your understanding and showcase your ability to manage regulatory projects effectively.
✨Tip Number 4
Prepare to discuss specific examples from your past experience where you've successfully navigated regulatory challenges. This will help you stand out during interviews and show how you can contribute to our team at StudySmarter.
We think you need these skills to ace Regulatory Specialist and Senior Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs, particularly in the medical devices sector. Emphasise any relevant projects you've managed and your familiarity with Quality Management Systems.
Craft a Compelling Cover Letter: In your cover letter, explain why you're passionate about regulatory affairs and how your skills align with the job requirements. Mention specific experiences that demonstrate your ability to create regulatory strategies and support risk management.
Showcase Your Technical Skills: Since the role requires excellent knowledge of Microsoft Office, be sure to mention your proficiency in Word, Excel, and OneDrive. Provide examples of how you've used these tools in previous roles, especially for data presentation and report generation.
Highlight Team Collaboration: The job involves providing training and support to colleagues, so include examples of how you've successfully collaborated with teams in the past. This could be through training sessions, project management, or cross-functional teamwork.
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulatory Frameworks
Familiarise yourself with the key regulations and standards relevant to medical devices. Be prepared to discuss how these frameworks influence product development and compliance, as this will demonstrate your expertise in the field.
✨Showcase Your Project Management Skills
Since project management skills are desirable for this role, be ready to share specific examples of projects you've managed. Highlight your ability to coordinate tasks, meet deadlines, and work collaboratively with cross-functional teams.
✨Prepare for Technical Questions
Expect questions that assess your understanding of Quality Management Systems and risk management processes. Brush up on your knowledge and be ready to explain how you have applied these concepts in your previous roles.
✨Demonstrate Your Communication Skills
As you'll be providing training and support to colleagues, it's crucial to showcase your communication abilities. Prepare to discuss how you've effectively conveyed complex regulatory information to non-experts in the past.
