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- Tasks: Join our team as an RA Specialist, ensuring healthcare products meet compliance and quality standards.
- Company: Medicareplus International leads in healthcare innovation, prioritising patient safety and product excellence.
- Benefits: Enjoy a competitive salary, professional development, flexible working options, and a supportive team environment.
- Why this job: Make a real impact in healthcare while collaborating on meaningful projects in a dynamic setting.
- Qualifications: Experience in regulatory affairs, strong knowledge of MDD and MDR, and excellent organisational skills required.
- Other info: Full-time, on-site role based in Wembley, London.
The predicted salary is between 36000 - 60000 £ per year.
Are you ready to make a difference in the healthcare sector? Do you have a keen eye for detail and a passion for regulatory compliance? Can you thrive in a dynamic, ever-evolving environment?
We are currently looking for a RA Specialist to join our busy team in Wembley, London! This is an exciting opportunity to play a pivotal role in ensuring our healthcare products meet the highest standards of compliance and quality.
Hours of Work:
Full-time & On-site
RA Specialist Duties:
- Maintain and promote regulatory compliance across the organisation.
- Provide operational input to cross-functional teams.
- Prepare crucial regulatory submissions.
- Ensure compliance documents are completed within designated timeframes.
- Engage in post-market surveillance activities.
- Generate technical documentation.
- Support international product registrations.
- Participate in audits and formulate Standard Operating Procedures.
RA Specialist Requirements:
- Experience in a regulatory affairs role, ideally within the medical device or healthcare sector.
- Strong knowledge of MDD, MDR, and other relevant regulatory standards.
- Excellent attention to detail and organisational skills.
- Ability to manage multiple tasks under tight deadlines.
- Strong problem-solving skills and proactive approach.
RA Specialist Benefits:
- Competitive salary.
- Opportunities for professional development and career advancement.
- Supportive and collaborative work environment.
- Contribution to meaningful projects that enhance patient safety.
- Flexible working arrangements considered.
Meet the Organisation: At Medicareplus International, we are at the forefront of healthcare innovation, dedicated to ensuring the highest quality and regulatory standards for our products. Our team thrives on collaboration and continuous improvement, focusing on enhancing patient safety and advancing product innovation.
If you think you are suitable for this RA Specialist role, please apply now and join us in making a meaningful impact in healthcare.
RA Specialist employer: Medicareplus International
Contact Detail:
Medicareplus International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land RA Specialist
✨Tip Number 1
Familiarise yourself with the latest regulations and standards in the healthcare sector, particularly MDD and MDR. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a fast-paced environment.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry events or join relevant online forums to connect with others who can provide insights and potentially refer you to opportunities within companies like ours.
✨Tip Number 3
Prepare to discuss specific examples of how you've managed compliance tasks or contributed to regulatory submissions in previous roles. Being able to articulate your experience clearly will set you apart from other candidates.
✨Tip Number 4
Showcase your problem-solving skills by thinking of scenarios where you overcame challenges in regulatory compliance. Highlighting your proactive approach will resonate well with our team, who values innovation and continuous improvement.
We think you need these skills to ace RA Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in regulatory affairs, particularly within the medical device or healthcare sector. Emphasise your knowledge of MDD, MDR, and any other regulatory standards that are pertinent to the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory compliance and your attention to detail. Mention specific examples of how you've successfully managed compliance tasks or contributed to audits in previous roles.
Highlight Key Skills: In your application, clearly outline your organisational skills, problem-solving abilities, and experience managing multiple tasks under tight deadlines. These are crucial for the RA Specialist position.
Show Enthusiasm for the Role: Convey your excitement about the opportunity to work at Medicareplus International and your commitment to enhancing patient safety. This can set you apart from other candidates who may not express the same level of enthusiasm.
How to prepare for a job interview at Medicareplus International
✨Know Your Regulations
Familiarise yourself with the Medical Device Directive (MDD) and Medical Device Regulation (MDR). Being able to discuss these regulations confidently will show your expertise and commitment to regulatory compliance.
✨Showcase Your Attention to Detail
Prepare examples from your past experience where your attention to detail made a significant impact. This role requires precision, so demonstrating this skill can set you apart from other candidates.
✨Demonstrate Problem-Solving Skills
Be ready to discuss specific challenges you've faced in previous roles and how you overcame them. Highlighting your proactive approach to problem-solving will resonate well with the interviewers.
✨Engage with the Team Spirit
Since the role involves collaboration, express your enthusiasm for teamwork. Share experiences where you successfully worked within a team to achieve a common goal, showcasing your ability to thrive in a supportive environment.
