Role: Senior Quality Engineer

Location: Irvine, CA - 92614

Duration: 06+ Months

Job Description:

Key Responsibilities:

• Work with new product development teams to help them efficiently navigate the Client’s Quality System in order to build quality system test samples and human use product according to project schedules
• Investigate moderately complex manufacturing product quality and compliance issues (e.g., non-conformances, CAPA, audit observations) for production processes prior to final product release based on engineering principles: analyze results, make recommendations and develop reports
• Optimize moderately complex manufacturing processes for design for manufacturing and for continuous process improvement. Identify opportunities to improve manufacturing processes and reduce risk. Drive improvements for inspection methods.
• Develop training and documentation materials for production (e.g., work instructions) to enable the seamless knowledge transfer of manufacturing processes
• Perform risk assessment on early-stage product manufacturing processes (e.g., PFMEAs, Manufacturing Process Reviews)
• Support test method validation activities for in-process inspections
• Facilitate Material Review Board to disposition potentially non-conforming human use products
• Track product yields and defect rates. Use data to report metrics at Quality Data Reviews and drive process improvements

Experience:

• Prior experience in medical device manufacturing or operations preferred.
• Experience with computerized Manufacturing Execution System (MES) preferred.