Regulatory Affairs Specialist

1 week ago


Weybridge, Surrey, United Kingdom Dentsply Sirona Full time

We are seeking an experienced Regulatory Affairs Specialist to join our team at Dentsply Sirona.

As a Regulatory Affairs Specialist, you will be responsible for maintaining and developing our local quality and pharmacovigilance management system, supporting product registrations with local competent authorities, and undertaking relevant training to deputise for the Responsible Person (RP). You will also manage various projects and ensure regulatory compliance with UK and Ireland regulations for Pharma and Medical Device distribution.

Earnings: The estimated salary for this role is £60,000 - £80,000 per annum.

Job Description:

  • ">
  • Maintain and develop the local quality and pharmacovigilance management system.
  • Support product registrations with local competent authorities.
  • Undertake relevant training to deputise for the Responsible Person (RP).
  • Manage various projects related to quality assurance and regulatory affairs.
  • Ensure regulatory compliance with UK and Ireland regulations for Pharma and Medical Device distribution.

Required Skills and Qualifications:

  • ">
  • Degree level education in a science, engineering, or medical discipline.
  • Experience within highly regulated environments (e.g. ISO 13485, GDMP).
  • Internal audit experience desirable.
  • Strong customer service and interpersonal skills.
  • High degree of accuracy and attention to detail.

Benefits:

  • ">
  • Attractive remuneration package.
  • 26 days' annual leave.
  • Attractive company pension scheme.
  • Flexible benefit scheme (including health insurance, dental cover, medical cash plan).


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