Senior Regulatory Affairs Lead, Medical Devices – Vascular

Abbott Laboratories seeks a Principal Regulatory Affairs Specialist to lead regulatory activities for vascular devices in the US, EU, and global markets. On-site in Santa Clara or Temecula, you will guide cross-functional teams and manage complex regulatory submissions across lifecycle stages.

The role requires strong knowledge of 21 CFR 820, ISO 13485, and EU MDR, with a proven track record in medical device regulatory leadership.