Our client is a leading medical device organisation who is a specialist in its field, due to their continued development they are looking to recruit an experienced Senior Specialist Regulatory.
The role will be responsible for regulatory oversight, planning, and management of new product development processes including registration submissions. This includes strategic planning, issue management, product compliance, and legislative tracking as well as overall management of new product development to meet regulatory and business deadlines and maintain the highest level of regulatory compliance.
To be considered for this position you must be degree educated with at least 3 years Regulatory affairs experience within the medical device sector. Exposure to Orthopaedics or Electro mechanical products is a highly preferred.
Candidates will need to be able to work independently and have excellent communication skills to work across the business to ensure their regulatory requirements are met.