£30000 per annum, Benefits: Private Medical and Life Cover
about 1 month ago
We are searching for a quality assurance/ regulatory affairs professional with previous experience within post market surveillance, vigilance, complaints handling to join an international medical device company.
This is a good platform to work closely with the wider business; partnering with your European colleagues and business units within a matrix organisation that has a global way of working and collaborating together.
This position will require previous Medical Device experience, working with ISO 13485, MDD and MDR requirements.
Supporting the Quality Manager and Engineers with QMS and SOP activities, auditing preparations and Post Market Surveillance activities.
Good working knowledge of regulations, quality systems and guidelines: CE Mark; Medical Device Directive / MDD MDR ; ISO 13485; ISO 14971; 21 CFR 820 US FDA requirements or other industry requirements.
If you are looking for a new opportunity like this, please send your CV and contact James Powell of TXM Recruit.
TXM Recruit is an equal opportunities employer. If you have any specific requirements or require assistance or reasonable adjustments to be made for you during the selection process due to disability or long-term health condition, we will do our best to assist you.