**What you will do:**

+ Lead quality issues with suppliers with Internal business partners; Lead effective supplier containment and corrections/corrective actions.
+ Act as point of contact for Internal/ External Customer groups on key compliance issues related to assigned suppliers.
+ Participate in External Audits and Internal Audits as needed. Ensure Regulatory compliance in area of responsibility to GMP of all medical device’s regulatory agencies (i.e. FDA, IMB, Notified bodies, etc.)
+ Management of SQA.
+ Responsible for accuracy and integrity of supplier data that ensures compliance with documented procedures & processes.
+ Ownership and reporting on all quality issues associated with the assigned suppliers. Ensure all assigned supplier related material quality issues are effectively communicated to key stakeholders.
+ Maintain structured communication channels with strategic sourcing, identifying responsibility by commodity / supplier.
+ Liaising w...