Orange County Metro Area, CA 92614 US
A global leader in the Medical Device industry, this company is looking to hire Engineer I.
Plan, organize, and prioritize complaint investigation activities based on complaint closure and reportability timelines.
Perform analysis in No Product Return Evaluations by utilizing multiple data inputs including technical review
of device history records (DHR review), in support of complaint investigations
Perform testing, assess results, and document routine complaint product device evaluations in support of complaint investigations
including dimensional and functional analysis.
Collaborate with other engineers on non-routine testing in support of failure investigation and root cause analysis.
Generate weekly complaint reports to provide data for weekly production meetings.
Bachelor s degree in scientific, Bio-Medical or engineering field, and previous quality compliance and medical device (Cardiovascular, endovascular, or other surgical products), healthcare, or a related environment required.
Good documentation, communication and interpersonal relationship skills including negotiating and relationship management skills
Solid problem-solving, organizational, analytical and critical thinking skills
Knowledge of and adherence to Quality systems
Strict attention to detail