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Job Details

Skills

QMS
Leadership
Team Building
Attention To Detail
Organized
ROOT
Reporting
Mentorship
Continuous Improvement
Medical Devices
Machining
Manufacturing
Regulatory Compliance
AS9100
ISO 13485
Management
GD&T
Inspection
Metrology
CMMS
Communication
Problem Solving
Conflict Resolution
Organizational Skills
Auditing
Quality Management
Documentation
Corrective And Preventive Action
Accountability
Quality Control
Quality Assurance

Summary

Direct Hire Quality Manager

Medical Device Manufacturing

Location: Hawthorne, Ca

Salary: $150K

Schedule: M- F: 7 AM -3:30P

We are seeking a Quality Manager to lead our Quality Management System (QMS), drive continuous improvement initiatives, and ensure the consistent production of high-precision, medical-grade components.

This is a hands-on leadership role responsible for quality assurance, compliance, audits, CAPA management, supplier quality, customer quality, and team development. The ideal candidate is detail-oriented, highly organized, and passionate about building a culture of quality and accountability.

Key Responsibilities

Maintain and improve the Quality Management System in compliance with ISO 13485, FDA Quality System Regulations, and customer requirements.
Lead internal audits, management reviews, and preparation for customer and regulatory audits.
Oversee incoming, in-process, and final inspection activities.
Manage calibration systems, metrology equipment, and inspection documentation.
Lead root cause investigations and corrective/preventive action (CAPA) activities.
Manage nonconforming materials, customer complaints, and quality-related corrective actions.
Serve as the primary point of contact for customer quality issues, audits, and inspections.
Oversee supplier quality activities, including evaluations, audits, and corrective actions.
Track and report quality metrics such as scrap, rework, customer complaints, audit findings, and CAPA effectiveness.
Lead, mentor, and develop Quality Inspectors, Quality Engineers, and other quality personnel.
Drive a culture of compliance, continuous improvement, and documentation discipline throughout the organization.

Qualifications

5+ years of quality experience in medical device manufacturing, precision machining, or another highly regulated manufacturing environment.
Experience maintaining compliance with AS9100 standards
Strong knowledge of ISO 13485 and FDA Quality System Regulations.
Experience managing Quality Management Systems, audits, CAPA programs, and quality documentation.
Understanding of GD&T, inspection methods, and metrology equipment, including CMMs.
Experience leading and developing quality teams.
Strong communication, problem-solving, and organizational skills.
Bachelor's degree in Engineering, Quality, or a related field preferred.

What Success Looks Like

Audit-ready quality systems and documentation.
Effective CAPA processes with timely closure and measurable results.
Reduced scrap, rework, and customer quality issues.
Strong supplier performance and customer confidence.
A well-trained, accountable, and high-performing quality team.

#ARROW
PandoLogic. Keywords: Quality Control / Quality Assurance Manager, Location: Hawthorne, CA - 90251

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: pandfeed
Position Id: 603886354
Posted 1 day ago

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