Our Medical Device Client is seeking a Quality Engineer for their team in Irvine, CA!
Quality Engineer
Duration - 3+ Months, Contract, W-2
Location - Onsite in Irvine, CA
Pay - $35 - 41 an hour
Job Description:
• This position is on the Quality Engineering team responsible for leading and performing critical engineering investigations on globally reported complaints for returned/non-returned devices.
• Ensure compliance with regulatory requirements and systems/procedures for device investigation and risk assessments of reported complaints from the field.
• Investigate complex manufacturing product quality and compliance issues reported from the field, analyze results, determine root cause/probable cause, and initiate and review reports.
• Perform hands-on device investigation using visual, dimensional, and test equipment to determine root cause
• Assess reported events against established risk documentation for clinical and compliance risk(s) and escalate to Quality Management and Product Safety as needed.
• Participate in escalation tasks and activities, including Project Risk Assessments (PRA) and Corrective/Preventive action(s) - CAPAs, SCARs, as determination by investigation.
• Identify and report key complaint metrics per device category and collaborate with applicable manufacturing engineering teams to resolve production/device related issues.
• Other incidental duties assigned by Leadership (May assist in Adhoc complaint analysis or metric review).
Education and Experience:
• Bachelor's degree in engineering, 0 - 2 years' experience related work experience required
• Experience in medical device (cardiovascular, endovascular, or other critical care/surgical products), healthcare, or a related environment preferred.
• Proficient with the Microsoft office suite
• Experience with medical device complaint investigations (CAPA's, NCR's, and Root-Cause Analysis)
• Functional, physical, and visual testing of medical device equipment in a laboratory setting
• Experience in complaint investigations, root cause analysis, and the associated risk assessments preferred.
Additional Skills:
• Good documentation, communication and interpersonal relationship skills including negotiating and relationship management skills
• Basic understanding of statistical techniques
• Previous experience working with lab/industrial equipment required
• Solid problem-solving, organizational, analytical and critical thinking skills
• Solid understanding of processes and equipment used in assigned work
• Knowledge of and adherence to Quality systems
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast-paced environment
• Must be able to work in a team environment, including the ability to manage project stakeholders
• Ability to build productive internal/external working relationships
All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry
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