Quality Engineering Manager, Production Support
Company Name:
Jacobs Management Group, Inc.
Title: Quality Engineering Manager, Production Support
Location: Tustin, California
Manages engineers and technicians to lead multiple quality assurance projects that support the manufacture of medical devices. Collaborates closely with Manufacturing, R&D, Regulatory and other Quality Assurance areas to support manufacturing process changes, product design improvements, implementation of new products and the enhancement of quality system compliance.
Responsibilities:
Manages a group of engineers and technicians that support the manufacture of medical devices
Manages quality engineers that work with Manufacturing Engineering and R&D to review process changes and resolve quality issues
Manages quality engineers that lead activities to investigate corrective actions associated with nonconforming product and customer complaints
Effectively communicates and collaborates with other departments as needed to achieve Quality Assurance and company goals
Manages quality engineers that lead projects to improve quality systems including projects that involve software based systems which collect and manage data
Works with suppliers to maintain high quality levels of incoming production materials
Performs other duties and responsibilities as assigned
Skills:
Excellent command of FDA and ISO medical device quality system requirements
Excellent ability to provide technical leadership in evaluating product quality issues
Excellent knowledge of medical product manufacturing and quality control
Ability to understand the technology related to the company's products
Computer skills including MS Word, Excel, and statistical software (preferably Minitab)
Experience with software used to manage quality informationEstimated Salary: $20 to $28 per hour based on qualifications.
Jacobs Management Group, Inc.
Title: Quality Engineering Manager, Production Support
Location: Tustin, California
Manages engineers and technicians to lead multiple quality assurance projects that support the manufacture of medical devices. Collaborates closely with Manufacturing, R&D, Regulatory and other Quality Assurance areas to support manufacturing process changes, product design improvements, implementation of new products and the enhancement of quality system compliance.
Responsibilities:
Manages a group of engineers and technicians that support the manufacture of medical devices
Manages quality engineers that work with Manufacturing Engineering and R&D to review process changes and resolve quality issues
Manages quality engineers that lead activities to investigate corrective actions associated with nonconforming product and customer complaints
Effectively communicates and collaborates with other departments as needed to achieve Quality Assurance and company goals
Manages quality engineers that lead projects to improve quality systems including projects that involve software based systems which collect and manage data
Works with suppliers to maintain high quality levels of incoming production materials
Performs other duties and responsibilities as assigned
Skills:
Excellent command of FDA and ISO medical device quality system requirements
Excellent ability to provide technical leadership in evaluating product quality issues
Excellent knowledge of medical product manufacturing and quality control
Ability to understand the technology related to the company's products
Computer skills including MS Word, Excel, and statistical software (preferably Minitab)
Experience with software used to manage quality informationEstimated Salary: $20 to $28 per hour based on qualifications.
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