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Skills
Aerospace and Defenseunmatched
Coachingunmatched
Continuous Improvementunmatched
Corrective Actionunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Customer Support/Serviceunmatched
Electricityunmatched
Engineering Managementunmatched
External Auditunmatched
FDA (Food and Drug Administration)unmatched
ISO (International Organization for Standardization)unmatched
Identify Issuesunmatched
Internal Auditunmatched
Leadershipunmatched
Lean Six Sigmaunmatched
Maintain Complianceunmatched
Manufacturingunmatched
Manufacturing Managementunmatched
Mechanical Engineeringunmatched
Medical Equipmentunmatched
Problem Solving Skillsunmatched
Productivity Managementunmatched
Quality Controlunmatched
Quality Engineeringunmatched
Quality Managementunmatched
Regulationsunmatched
Riskunmatched
Risk Managementunmatched
Root Cause Analysisunmatched
Supply Chain Operationsunmatched
System Testunmatched
Team Lead/Managerunmatched
Time Managementunmatched
Trend Analysisunmatched
Willing to Travelunmatched
Description
Our client is seeking an experienced Senior Quality Manager to own manufacturing quality performance, including inspection activities, NCR/MRB processes, CAPA, and quality systems execution. This role is highly visible within operations and requires strong leadership, cross‑functional collaboration, and hands‑on shop‑floor engagement.
Onsite | No Visa Sponsorship | No Relocation Assistance
Responsibilities:
Audit Support: Support internal/external audits, including regulatory inspections.
Supplier Quality: Support incoming material quality and vendor‑related troubleshooting.
Quality Reporting: Provide leadership with data‑driven reporting on quality, performance and risk.
NCR/MRB Ownership: Lead investigation, disposition, trending, and timely closure of nonconformances.
CAPA & Root Cause: Drive corrective actions based on manufacturing trends and structured root‑cause analysis.
Manufacturing Quality Leadership: Lead all manufacturing‑related quality activities across production operations.
Inspection & Product Release: Oversee in‑process inspection, final inspection, product acceptance, and release.
Team Management: Manage Quality Engineers, the QC Supervisor, and inspection teams; coach and develop staff.
Continuous Improvement: Apply Lean, Six Sigma, and risk‑reduction methodologies to improve yield and efficiency.
Quality Systems & Compliance: Ensure compliance with ISO 13485, FDA QMSR, and other applicable regulations.
Cross‑Functional Collaboration: Partner with Manufacturing, Engineering, Supply Chain, and Operations to resolve issues.
Qualifications (Must-Haves)
3+ years managing Quality Engineers and/or QC teams.
Ability to travel 5–10% for vendor support, customer visits, and system testing.
Bachelor's degree in Engineering (Mechanical, Electrical, or related) or equivalent experience.
Strong knowledge of ISO 13485, risk‑based quality principles, and regulated QMS requirements.
Hands‑on ownership of manufacturing quality, including NCR/MRB, CAPA, and shop‑floor execution.
8+ years of progressive Quality experience in regulated manufacturing (medical device required; aerospace/defense/IVD acceptable with relevant crossover)