Regulatory Affairs Associate

Regulatory Affairs Associate
  • £30,000 - £38,000 per Annum
  • Permanent
  • Cheshire, England, UK CW7 3RT Cheshire UK CW7 3RT
Job Ref: J35314
Sector: Clinical
Sub-sector: Medical Devices
Date Added: 12 May 2020
Regulatory Affairs Associate - Medical Devices - Post Market Surveillance

Regulatory Affairs Associate - Medical Devices - Post Market SurveillanceSRG are currently recruiting for a Regulatory Affairs Assocaite to join a Medical Device company in Cheshire on a permanent basis on a competitive salary and benefits package, depending on experience.Reporting to the Regulatory Affairs Manager, you will be responsible for maintaining the Post Market Surveillance process to support the design, development and ongoing commercialisation of products and maintaining the vigilance system for the company's product portfolio.Skills & Experience* Degree, or equivalent qualification, in a Life Science, or equivalent industry experience* Knowledge of relevant GMP and Quality Systems standard, specifically with FDA Quality System Regulation and ISO 13485 relevant to this role* Understanding of the European Medical Devices Regulation (MDR) relevant to this role* Experience of working in a regulated environment* Understanding of Risk Management within a Medical Device industry* Ability to query and analyse data* Demonstrated organisational skills* Ability to work under pressure to meet process/project time frames, regulatory requirements and company requirements* Competent IT skill in preparing files. * The ability to influence and challenge others in a constructive way so as to deliver improvements.* Excellent communication skills both written and verbally with employees, customers, in country agents and Regulatory Authorities.For more information, please call Laith Mustafa on 0161 868 2231 or email

11/06/2020 13:30:53
GBP 30000 30000
Contact Consultant:
Laith Mustafa

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