Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- 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 conversations. This will show that you have the relevant connections and knowledge that RRxCo is looking for.
✨Tip Number 2
If you have experience in team management, be prepared to discuss specific examples of how you've led projects or teams in the past. This will demonstrate your leadership skills, which are crucial for this role.
✨Tip Number 3
Engage with professionals in the Medtech industry through LinkedIn or relevant forums. Building relationships with others in the field can lead to valuable insights and potential referrals for the position.
✨Tip Number 4
Familiarize yourself with the latest trends and regulations in the Medical Device sector. Being knowledgeable about current challenges and innovations will help you stand out as a candidate who is proactive and informed.
We think you need these skills to ace Regulatory Affairs Consultant
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Consultant position. Understand the key responsibilities and required qualifications, especially the importance of experience in Life Science Regulatory Affairs.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 4-10 years of experience in Regulatory Affairs within the Medical Device, Pharmaceutical, or Biotechnology sectors. Be specific about your past roles and how they relate to the requirements of this position.
Showcase Leadership Skills: Since the role requires a natural people/project leader, include examples of your team management experience. Highlight any projects where you led a team or collaborated with regulatory authorities like MHRA, CQC, and BSI.
Tailor Your Application: Customize your application materials to reflect the specific needs of RRxCo. Use keywords from the job description and demonstrate your understanding of both local and global regulatory environments.
How to prepare for a job interview at RRxCo.™
✨Show Your Regulatory Expertise
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 challenges.
✨Demonstrate Leadership Skills
Since the role requires a natural people/project leader, share examples of your past team management experiences. Discuss how you motivated your team and ensured that milestones were met.
✨Familiarize Yourself with Regulatory Authorities
Brush up on your knowledge of the MHRA, CQC, and BSI. Be ready to discuss your past interactions with these authorities and how you handled any regulatory submissions or audits.
✨Prepare for Onsite Presence Discussion
Since the position requires onsite presence in the Midlands, be ready to discuss your availability and willingness to work onsite for the first 6 months. This shows your commitment to the project and the team.
