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 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: · Five years plus experience within the medical device industry in Post market surveillance and complaints(Minimum)
To get in touch please contact Jack Forbes on 0203 0196 024 or email@example.com with 100% confidentiality.