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Senior Quality Assurance Manager
Job in
Trenton, Mercer County, New Jersey, 08628, USA
Listed on 2026-07-27
Listing for:
Interactive Resources - iR
Full Time
position Listed on 2026-07-27
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below
We are seeking an experienced and results-driven Senior Quality Manager to lead all site quality functions within a manufacturing environment. This role serves as the site’s Quality Management Representative and is responsible for driving a culture of quality, continuous improvement, and operational excellence while ensuring compliance with customer, corporate, and regulatory requirements.
Key Responsibilitie- sLead all quality functions, including Quality Control, Quality Engineering, Validation, Metrology, and Quality Systems
- .Drive continuous improvement initiatives to enhance product quality, operational efficiency, and customer satisfaction
- .Develop and monitor quality metrics, KPIs, and performance objectives
- .Maintain and improve the Quality Management System (QMS) to ensure compliance with applicable standards and regulations
- .Serve as the primary point of contact for audits, regulatory inspections, and customer quality matters
- .Lead internal audits, corrective actions, and compliance initiatives
- .Support customer complaint investigations, root cause analysis, and corrective actions
- .Provide technical quality support for manufacturing, including validation, process improvements, SPC, and data analysis
- .Build, mentor, and develop a high-performing quality team
- .Deliver training programs and support employee development within the quality organization
- s:
Bachelor’s degree in Engineering, Quality, Science, Business, or a related technical fiel - d.Minimum of 7 years of experience in quality management within a manufacturing environmen
- t.At least 3 years of leadership experience managing team
- s.Experience in regulated industries such as medical device, pharmaceutical, or healthcare packaging preferre
- d.Strong knowledge of Quality Management Systems and regulatory standards (FDA 21 CFR Part 820, ISO 13485, ISO 9001
- ).Experience with validation, Statistical Process Control (SPC), process capability, and continuous improvement tool
- s.Proficiency with ERP systems, QMS platforms, and Microsoft Offic
Position Requirements
10+ Years
work experience
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