Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Design Quality Engineer
Job
L&T Technology Services
Los Angeles, CA (In Person)
$81,452 Salary, Full-Time
Review key factors to help you decide if the role fits your goals.
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
77
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Design Quality Engineer at L&T Technology Services Design Quality Engineer at L&T Technology Services in Canoga Park, California Posted in about 20 hours ago.
Type:
full-timeJob Description:
Job Description & Skill Requirement:
- Evaluate product issues to ensure patient, user and security risk are assessed, and acting as the lead Design Quality Engineer for Post-Market Design Changes on Capital Hardware
- Update DFMEA and DHF documents as needed as part of the post market design change management process
- Provide comprehensive support to Post Market Development Teams with a focus on Design Quality and Risk Management
- Collaborate with different departments across the organization to understand and review data to assess the patient/user risk associated with the post market life-cycle phase
- Support Complaint trending and Severity trending signal dispositions
- Maintain risk management file throughout product lifecycle, ensuring the latest knowledge on risk reflected in the risk documentation
- Assure compliance to organizational procedures, regulatory requirements and industry standards, and timely completion of assigned CAPAs and audit findings
- Makes decisions and proposes solutions based on calculated risks identified through data analysis
- Assist with protocol and implement process validation procedures in accordance with QSR, FDA and international guidelines
- Coordinate activities through the Quality Engineering Manager and report regularly on the progress of activities
Qualification:
- Bachelors degree required
- Minimum of 7 years of relevant experience, or advanced degree with a minimum of 5 years relevant experience
- Excellent communication and technical writing skills
- Experience in Manufacturing and/or Electro-Mechanical Medical Device risk assessments
- Working knowledge of Quality System Regulation (QSR 21 CFR 820) and EU Medical Device Directive (EU