Overview

Quality Assurance Manager – Manufacturing Jobs in Oxnard, CA at Kinect

Title: Quality Assurance Manager – Manufacturing

Company: Kinect

Location: Oxnard, CA

This role is fully onsite in Oxnard, California.

Quality Assurance Manager

Location: West Ventura County

Industry: High-Tech Manufacturing (AS9100 Certified)

A leading high-tech manufacturer in West Ventura County is seeking an energetic and experienced Quality Assurance Manager. As the performance and quality leader in our field, we produce advanced connector and lighting systems that enhance safety and efficiency in the Marine, Military, and Nuclear Power Generation industries.

The QA Manager holds ultimate responsibility for the Quality Management System (QMS) across design, manufacturing, and supply operations. This role collaborates closely with Manufacturing and Engineering leadership to maintain and enhance quality systems while driving continuous improvement in safety, financial performance, employee development, and customer satisfaction. The QA Manager will also lead efforts toward achieving ISO 45001, ISO 14001, and ISO 50001 certifications.

Key Responsibilities

Policy Implementation

Interpret and implement quality assurance standards.

Draft and oversee implementation of company quality policies and procedures.

Review and update the Quality Manual as needed.

Reporting & Risk Management

Collect, analyze, and report statistical quality data to monitor performance and identify areas for improvement.

Measure and report quality costs, driving continuous reduction efforts.

Monitor and assess risk management activities.

Oversee customer supplier scorecards and report results.

Provide monthly reports to senior management on NCRs, RMAs, CAPAs, and quality costs.

Deliver quarterly reports on QA program effectiveness, including recommendations for corrective and preventive actions.

Quality Assurance & Compliance

Ensure customer requirements and expectations are met for all products and documentation.

Oversee Verification and Validation activities.

Evaluate and monitor procurement sources for compliance with quality requirements.

Investigate and resolve customer complaints and non-conformance issues, including root cause analysis and corrective actions.

Operate the Material Review Board and oversee disposition of nonconforming items.

Manage the quality audit process, including internal and external audits.

Develop a company-wide quality culture through training, enforcement of quality processes, and continuous improvement initiatives.

Oversee maintenance of quality records and documentation.

Recruit, train, and manage quality team members.

Quality Control & Metrology

Supervise quality control (QC) laboratory activities, including inspection and testing of materials, components, and final products.

Mentor and develop QC staff to enhance skills and expertise.

Oversee calibration and repair of all test and measurement equipment.

Manage incoming and in-process inspections, including first-article inspections.

Qualifications

Bachelor’s degree in Manufacturing Engineering or a related field from an accredited four-year institution.

10+ years of quality management experience in a medical device or aerospace manufacturing environment.

ASQC Certification REQUIRED

Experience in a leadership, supervisory, or management role.

Proven expertise in managing an AS9100-certified quality system.

Experience implementing ISO 45001, ISO 14001, and/or ISO 50001 is a plus.

This position offers the opportunity to play a critical role in maintaining and advancing a world-class quality assurance program within a high-tech, AS9100-certified manufacturing environment.

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