Orange County Metro Area, CA 92618 US
A global leader in the Medical Device industry, this company is looking to hire Quality Engineer I.
Investigate and/or provide input on non-conformance events (NC) and Corrective Actions and Preventive Actions (CAPA).
Will lead mixed product events and will perform quality approvals on minor nonconformance events.
Track and trend NC and CAPA data with guidance using various statistical and non-statistical problem-solving tools as part of analysis.
Lead (primary) and support the reduction of recurring nonconformance events, reprocessing events, and scrap.
Uses various statistical and non-statistical problem-solving tools as part of analysis of data, issues, or improvement opportunities.
BSc. in Engineering (Preferred Mechanical, Electrical, or Manufacturing)
1 - 3 years experience in industry. Medical device, consumer, automotive, and aerospace preferred.
Preferred 1 - 2 years experience in new product introductions/quality/manufacturing/ manufacturing science and technology/technical development/R&D.
Understanding of manufacturing processes and related process equipment.
Working knowledge of applied statistics, quality systems and regulatory requirements across multiple health authorities