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- Tasks: Lead regulatory affairs projects for a top Medtech manufacturer in the UK.
- Company: Join RRxCo, a dynamic company focused on innovative medical solutions.
- Benefits: Enjoy a 12-month project with potential for growth and valuable industry experience.
- Why this job: Make an impact in healthcare while collaborating with experts in a supportive environment.
- Qualifications: 4-10 years in Life Science Regulatory Affairs; team leadership and regulatory authority experience required.
- Other info: Onsite presence needed in the Midlands for the first 6 months, ideally 3 days a week.
The predicted salary is between 43200 - 72000 £ per year.
RRxCo is seeking a Regulatory Affairs Consultant to assist with a 12-month initial project for a leading Medical Device (Medtech) manufacturer to support several activities in the overall program. The program will based in the United Kingdom, with some onsite presence needed at one of their sites in the Midlands (for the first 6 months, ideally 3 days a week). You will be responsible for the delivery of the output from several specialists within the regulatory affairs group to ensure department milestones are met. Requirements 4 – 10 years of Life Science Regulatory Affairs (RA) experience in a Medical Device, Pharmaceutical or Biotechnology setting. Natural people/project leader. Past experience of team management. Past working and interactions with regulatory authorities (MHRA, CQC and BSI). Ideally both local and global regulatory exposure
Regulatory Affairs Consultant employer: RRxCo.™
Contact Detail:
RRxCo.™ Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Consultant
✨Tip Number 1
Make sure to highlight your experience with regulatory authorities like MHRA, CQC, and BSI during networking events or informational interviews. This will show your familiarity with the UK regulatory landscape, which is crucial for this role.
✨Tip Number 2
Connect with professionals in the Medtech industry on platforms like LinkedIn. Engaging with their content or reaching out for a chat can help you learn more about the company culture and expectations, giving you an edge in your application.
✨Tip Number 3
Consider attending industry conferences or webinars focused on regulatory affairs in the medical device sector. This not only expands your knowledge but also helps you meet potential colleagues and decision-makers from RRxCo.
✨Tip Number 4
If you have past experience managing teams, be prepared to discuss specific examples of how you led projects to success. This will demonstrate your leadership skills, which are essential for the Regulatory Affairs Consultant position.
We think you need these skills to ace Regulatory Affairs Consultant
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your 4-10 years of experience in Life Science Regulatory Affairs, particularly in the Medical Device, Pharmaceutical, or Biotechnology sectors. Use specific examples to demonstrate your expertise.
Showcase Leadership Skills: Since the role requires a natural people/project leader, include instances where you have successfully managed teams or projects. Highlight your ability to lead and motivate others.
Detail Regulatory Interactions: Discuss your past experiences working with regulatory authorities such as MHRA, CQC, and BSI. This will show your familiarity with the regulatory landscape and your capability to navigate it effectively.
Tailor Your Application: Customize your CV and cover letter to align with the specific requirements of the position. Mention your local and global regulatory exposure to demonstrate your comprehensive understanding of the field.
How to prepare for a job interview at RRxCo.™
✨Showcase Your Regulatory Experience
Make sure to highlight your 4-10 years of experience in Life Science Regulatory Affairs. Be prepared to discuss specific projects you've worked on, especially in the Medical Device sector, and how you navigated regulatory requirements.
✨Demonstrate Leadership Skills
As a natural people/project leader, it's important to convey your team management experience. Share examples of how you've successfully led teams, resolved conflicts, and motivated others to meet project milestones.
✨Familiarize Yourself with Regulatory Authorities
Since the role involves interactions with regulatory authorities like MHRA, CQC, and BSI, brush up on their processes and recent changes in regulations. Being knowledgeable will show your commitment and readiness for the role.
✨Prepare for Onsite Presence Discussion
Given the requirement for onsite presence in the Midlands, be ready to discuss your availability and willingness to commute. This shows your flexibility and commitment to the project’s needs.
