This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
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.
#J-18808-Ljbffr
Worksite address
temecula, CA, 92591, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.