Job Description
A leading medical device company located in Tijuana, Baja California, is seeking an experienced professional for the role focused on Quality & Regulatory Compliance. The ideal candidate will own the Quality Management System and ensure compliance with FDA and ISO standards. This individual will lead audits, manage supplier compliance, and develop training programs while promoting a culture of quality and accountability. Strong experience in medical device manufacturing, alongside excellent communication skills, is essential for this role.
#J-18808-Ljbffr
#J-18808-Ljbffr
Ready to Apply?
Submit your application today and join our talented team at Grupo TECMA.
Submit ApplicationJob Details
- Location tijuana, tijuana
- Job Type Full-time
- Category Other-General
- Posted Date June 23, 2026
- Application Deadline August 02, 2026