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RA Specialist

Medicareplus International
Posted a day ago, valid for 24 days
Location

Wembley, Greater London HA0, England

Salary

£35,000 - £42,000 per annum

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Contract type

Full Time

In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The position of RA Specialist is available in Wembley, London, focusing on regulatory compliance in the healthcare sector.
  • Candidates should have experience in a regulatory affairs role, preferably in the medical device or healthcare sector, with a strong knowledge of MDD and MDR standards.
  • The role involves preparing regulatory submissions, maintaining compliance documents, and participating in audits, all within a full-time, on-site work environment.
  • A competitive salary is offered along with opportunities for professional development and a supportive work culture.
  • If you are detail-oriented and passionate about enhancing patient safety, this role is an exciting opportunity to make a difference.

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:

As an RA Specialist, you will be instrumental in maintaining and promoting regulatory compliance across the organisation. Your responsibilities will encompass providing operational input to cross-functional teams, preparing crucial regulatory submissions, and ensuring compliance documents are completed within designated timeframes. You'll also engage in post-market surveillance activities, generate technical documentation, and support international product registrations. Furthermore, participation in audits and the formulation of Standard Operating Procedures will be key aspects of your role, all within a supportive team environment.

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: Who We Are and What We Do

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!

Apply now in a few quick clicks

In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.