Multiple CER and PMS roles - Limerick

Job Reference: #42906 Add to saved jobs

  • Location Ireland
  • Contract
  • Sector Medical Devices

Job Summary

Summary: Meet is joining with a International Consultancy and is looking to speak with QA professionals who possess PMS and complaints experience. this role will be based in south west Ireland and will be on a 6 month contract. 

Job Overview

Job Responsibilities: As the Regulatory Affairs Specialist you will be responsible for: Lead investigations into product complaints and other post marketing surveillance reports, complying with relevant regulations; Proactively identify and lead complaint reduction and product performance improvement programs; Maintain post marketing surveillance standard operating procedures, ensuring compliance with relevant parent global policies and procedures and applicable regulations; Support preparation and development of Annual Product Quality reviews and other periodic quality management reviews; Lead/support Risk Management System activities;

Skills Required

Skills Required: ·         Five years plus experience within the medical device industry in Post market surveillance and complaints(Minimum)

Contact Details

To get in touch please contact Jack Forbes on 0203 0196 024 or with 100% confidentiality.

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