Quality Manager

Quality Manager Suitable Staffing Solutions Carson, CA Job Details Full-time $120,000 - $150,000 a year 1 day ago Benefits Health insurance Dental insurance Vision insurance Qualifications Quality control corrective actions ISO standards Regulatory compliance Dimensional inspection Compliance audits & assessments GD&T Bachelor's degree Manufacturing Root cause analysis

PPAP FDA

regulations Measurement (quality control) Full Job Description Position Summary The Quality Manager is responsible for leading and maintaining a compliant, audit‑ready

ISO 13485

Quality Management System while ensuring consistent delivery of high‑precision, medical‑grade components. This role oversees all quality functions—including inspection, metrology, document control, CAPA, supplier quality, and customer quality—and drives a culture of accountability, continuous improvement, and documentation discipline across the organization. Key Responsibilities Quality Management System Maintain and improve the QMS in compliance with

ISO 13485, FDA QSR

(21 CFR 820), and customer‑specific requirements. Ensure all procedures, work instructions, forms, and records are controlled, current, and properly implemented. Lead internal audits, management reviews, and readiness for customer and regulatory audits. Inspection & Metrology Oversee incoming, in‑process, and final inspection activities. Manage calibration, gage control, and metrology equipment (CMMs, vision systems, hand tools). Ensure proper use of GD&T, sampling plans, and inspection documentation. CAPA, NCR, and Root Cause Lead structured root‑cause investigations using 5‑Why, Fishbone, DMAIC, or similar tools. Drive timely and effective CAPA implementation, verification, and closure. Manage nonconformances, deviations, concessions, and customer notifications. Customer & Supplier Quality Serve as the primary point of contact for customer quality issues, audits, and source inspections. Manage supplier evaluations, audits, scorecards, and corrective actions. Support customer documentation requirements (FAIRs, PPAP, validation, risk management). Team Leadership Lead, mentor, and develop Quality Inspectors, Document Control, and Quality Engineers. Set clear expectations, provide coaching, and ensure accountability for performance and documentation accuracy. Build a culture of quality, compliance, and continuous improvement. Quality Metrics & Reporting Track and report

KPIs:

scrap, rework, yield, audit findings, customer complaints, and CAPA performance. Present quality performance to leadership and drive data‑based improvement initiatives. Qualifications 5+ years of quality experience in medical device manufacturing, precision machining, or regulated production. Strong knowledge of

ISO 13485, FDA

QSR, and GD&T. Experience leading audits, managing CAPA, and maintaining a compliant QMS. Proficiency with metrology tools, CMMs, and inspection software. Demonstrated leadership ability in a fast‑paced manufacturing environment. Excellent communication, documentation, and problem‑solving skills. Bachelor's degree in Engineering, Quality, or related field preferred. If you are interested in the position, please come in to apply in person at 801 W Victoria St, Suite A-1, Compton, CA 90220, or give us a call for more information at 310 668-9088. Please send your resume to

Pay:

$120,000.00 - $150,000.00 per year

Benefits:

Dental insurance Health insurance Vision insurance

Work Location:

In person