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Senior Regulatory Specialist

Hunter Selection
Posted 14 days ago, valid for 11 days
Location

Cardiff, South Glamorgan CF24 0TB, Wales

Salary

£48,000 - £57,600 per annum

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Contract type

Full Time

Employee Assistance

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Sonic Summary

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  • The Senior Regulatory Specialist position is based in Cardiff and requires experience in Regulatory Affairs, specifically within the medical device sector.
  • Candidates must have Class 2A/B medical device experience and the ability to lead regulatory activities and manage compliance enquiries independently.
  • The role offers a highly competitive salary, a bonus opportunity, and a generous benefits package including 25 days of holiday, a matched 5% pension, and discounts at local establishments.
  • Responsibilities include designing and implementing quality management systems, preparing submissions, and developing regulatory strategies for new product development.
  • The organization is rapidly growing and aims to significantly increase its workforce due to rising market demand.

Senior Regulatory Specialist

Cardiff CF14

Commutable from Cardiff, Newport, Bridgend, Caerphilly, Barry, Llantrisant, Pontypridd

Benefits:-

  • Highly competitive salary
  • Bonus Opportunity
  • 25 Days + Bank Holidays
  • Employee assistance programme
  • Matched 5% pension
  • Funded company social events
  • Free on-site parking and secure cycle shelter
  • Discounts at local restaurant and local gym

Are you an experienced Regulatory Affairs professional? This could be the perfect opportunity for you to join a rapidly growing organisation working with a product has a genuine positive impact on the end user. The business has exciting plans to significantly increase the headcount on site due to increased market share and orders. This role will provide you with a generous benefits package including a matched 5% pension, alongside excellent soft benefits.

Responsibilities

  • Design and implement QMS for design control
  • Be part of NPD team and remediation activities to prepare and maintain technical files to ensure continuous compliance.
  • Preparation of submissions and communication with regulatory organisations.
  • Develop and implement regulatory strategy for NPD and existing products to maintain compliance.
  • Submission of regulatory applications and communications with international regulatory approvals.
  • Surveillance of new standards and ensuring NPD meets recognise consensus standards.

Requirements

  • Medical Device experience is an essential for this role.
  • Able to lead RA activities and be the first point of contact for compliance enquiries.
  • Able to manage day-to-day activities and tasks, and work independently in RA matters.
  • Class 2A/B medical device experience.
  • Good regulatory application knowledge.

24228/617

If you are interested in this role or looking for something similar please contact Jack Lavis directly at (url removed) or call for a confidential discussion on (phone number removed).

If you are interested in this position please click 'apply'.

Hunter Selection Limited is a recruitment consultancy with offices UK wide, specialising in permanent & contract roles within Engineering & Manufacturing, IT & Digital, Science & Technology and Service & Sales sectors.


Please note as we receive a high level of applications we can only respond to applicants whose skills & qualifications are suitable for this position. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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