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- Tasks: Join our team as an RA Specialist, ensuring healthcare products meet compliance standards.
- Company: Medicareplus International leads in healthcare innovation and quality assurance.
- Benefits: Enjoy a competitive salary, professional development, and flexible working options.
- Why this job: Make a real impact on patient safety while thriving in a supportive team environment.
- Qualifications: Experience in regulatory affairs, strong attention to detail, and problem-solving skills required.
- Other info: Full-time, on-site role in Wembley with opportunities for career advancement.
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? 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.
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 in Wembley employer: Medicareplus International
Contact Detail:
Medicareplus International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land RA Specialist in Wembley
✨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 dynamic field.
✨Tip Number 2
Network with professionals in the regulatory affairs community. Attend industry events or join relevant online forums to connect with others in the field. This can provide valuable insights and potentially lead to referrals for the RA Specialist position.
✨Tip Number 3
Prepare to discuss specific examples of how you've ensured compliance in previous roles. Highlight your attention to detail and problem-solving skills by sharing stories that showcase your ability to manage multiple tasks under tight deadlines.
✨Tip Number 4
Research Medicareplus International thoroughly. Understand their products, values, and recent developments in the company. Tailoring your conversation during interviews to reflect this knowledge can set you apart from other candidates.
We think you need these skills to ace RA Specialist in Wembley
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the RA Specialist position. Understand the key responsibilities and requirements, such as knowledge of MDD and MDR, to tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience in regulatory affairs, particularly within the medical device or healthcare sector. Use specific examples to demonstrate your attention to detail and problem-solving skills.
Craft a Compelling Cover Letter: Write a personalised cover letter that showcases your passion for regulatory compliance and how your skills align with the company's mission. Mention your ability to thrive in dynamic environments and your commitment to enhancing patient safety.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for the RA Specialist role.
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 could be in preparing regulatory submissions or ensuring compliance documents are accurate and timely.
✨Demonstrate Problem-Solving Skills
Be ready to discuss specific challenges you've faced in previous roles and how you approached solving them. Highlighting your proactive approach will resonate well with the interviewers.
✨Engage with the Team Spirit
Since the role involves collaboration, express your enthusiasm for working in a team environment. Share experiences where you successfully collaborated with cross-functional teams to achieve common goals.
