Position: Sr Regulatory Consultant
Location: Andover, MA
Duration: 3-12 months (Extendable Contract)
Please contact for more detailed JD
In this role, you have the opportunity to guide and support the EU MDR Program and the Business Groups in EU regulations. This involves being a confident advisor on regulatory strategy, lobbying, regulatory compliance and quality management related topics, in order to achieve systems and product compliance as well as to support other laws, regulations and standards impacting safe and effective utilization in the EU.
Own and drive activities within the EU MDR Program as a Subject Matter Expert. Define and support training with information/guidance documents on MDD/MDR/IVDR/MEDDEV 2.7/rev4 as appropriate within the businesses and supporting functions. Consultation on MDR/IVDR (internally & externally) to drive our position and maintain awareness of industry (competitor) positionin