California Licensed Engineer II

A company is looking for an Engineer II, Post Market Surveillance.

Key Responsibilities

Participate in and own escalation tasks including Product Risk Assessments and Corrective / Preventive actions

Identify and manage improvement projects to optimize internal processes using engineering methods

Report key complaint metrics and collaborate with manufacturing / R&D teams to address device-related issues

Required Qualifications and Education

Bachelor's degree in Engineering or a Scientific field with a minimum of 2 years of experience in the medical device or pharmaceutical industry

Hands-on experience managing processes in highly regulated environments

Advanced degree in a relevant field is preferred

Knowledge of MDR and FDA regulations related to the medical device industry

Proficiency in MS Office Suite and relevant software tools