After a high volume of applications, we are pleased to announce that our new Quality Manager has been chosen and has now commenced work with our company.

They will continue to maintain our existing ISO 13485:2016 system, further developing and improving processes in line with our business needs. They will also lead our transition from MDD to MDR in advance of the 2024 deadline.

Our Quality Manager is a Microbiologist and highly accomplished Regulatory and Quality Professional. He has been a lead auditor assisting a Notified Body and Healthcare companies, with assessments conducted against applicable regulatory requirements such as MDD, MDR and Quality Management Systems such as ISO13485.

He has experience of evaluating the performance of over 500 plus small, medium and large healthcare companies and identifying areas for improvement to meet a range of regulatory requirements. Such activities include conducting unannounced audits across the globe; implementing updates to quality management systems; establishing updates to product technical documentation for class III implantable devices, class IIb RF devices and class I sterile and reusable instruments. 

His comprehensive knowledge and experience within the medical device arena will be an asset to our Company, as we continue to build our team.

Thank you to all the other candidates who applied. Those shortlisted have all been notified and we would like to wish them luck with finding a suitable position in the near future.