05 oct
|
Grupo TECMA
|
Tijuana
05 oct
Grupo TECMA
Tijuana
Grupo TECMA in Mexico seeks a seasoned Quality & Regulatory Compliance professional to own and maintain the QMS, lead FDA and ISO audits, and drive CAPA and risk management programs. You will collaborate across Manufacturing Engineering, Quality, Supply Chain, and Operations to embed compliance in daily operations.
The role requires deep regulatory knowledge (FDA QMSR, ISO 13485) and fluent English for audits and executive communication.
📌 Senior Medical Device Compliance Officer (Tijuana)
🏢 Grupo TECMA
📍 Tijuana