A global medical device company seeks a Director for Post-Market Surveillance and Clinical Evaluation to lead global strategy, governance, and compliance across markets. The role requires extensive experience in a regulated industry, strong leadership, and effective communication skills. Responsibilities include ensuring regulatory alignment and fostering a high-performance culture within the team. Candidates must possess a third-level qualification in a relevant field and have a minimum of 12 years' experience in similar roles. The position is full-time and based in Bloomington, Indiana.
#J-18808-Ljbffr