**Summary**:
The QAE will be pulling and analyzing Complaint Data to support Risk Management / Postproduction Control. Responsible for planning, implementing, and managing compliance of post market monitoring processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution.
**Responsibilities**:
- Designs, implements, and maintains quality assurance protocols and methods for Analyzing Complaint Data.
- Designs methods and procedures for inspecting, testing and evaluating the precision and accuracy of post-production processes.
- Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary.
- May assure compliance to in-house and/or external specifications and standards (i.e. GLP, GMP, ISO, Six Sigma).




- Works on problems of a moderate scope where analysis of situation or data requires a review of a variety of factors.
- Normally receives general instructions on routine work and detailed instructions on new projects or assignments.
**Qualifications**:
- Professional degree in Engineering.
- Must possess 2 years of minimum experience in a FDA Regulated environment (medical industry), or 4 years as QA Engineer in any other regulated QA system.
- Fluent in English.
**KINDLY UPLOAD YOUR RESUME IN ENGLISH.**
Application Question(s):
- What is your minimum gross daily salary requirement (Before taxes)?
**Experience**:
- Medical Industry: 2 years (preferred)
**Language**:
- advanced English level (preferred)
Work Location: In person

📌 QA Engineer (Tijuana)
🏢 Enovis México
📍 Tijuana