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Sterling Engineering
Quality Assurance Project Manager
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What they do
A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.
$106,008 / year median in Illinois
-2% projected decline
Job Description
Quality Assurance Project Manager at Sterling Engineering Quality Assurance Project Manager at Sterling Engineering in Lincolnshire, Illinois Posted in 4 days ago.
Type:
full-timeJob Description:
Quality Assurance Project Manager Location:
Buffalo Grove, IL Hire Type:
Direct Hire | Full-Time | 100%Onsite Compensation:
$125,000-$130,000 Base Salary + 10%Annual Bonus Benefits:
Comprehensive benefits package including medical, dental, vision, 401(k), paid time off, paid holidays, and additional company-sponsored benefits. Overview We are seeking an experienced- Quality Compliance Manager
- to lead Quality Systems and Regulatory Compliance activities within a highly regulated medical device manufacturing environment.
- Lead and support the site's Quality Compliance function, ensuring compliance with all regulatory and quality system requirements.
- Develop, implement, and maintain internal Quality Management System (QMS) audit programs.
- Plan, schedule, and execute internal quality system audits across manufacturing and support functions.
- Prepare audit plans, audit checklists, reports, and maintain all required audit documentation.
- Identify quality trends, nonconformances, and opportunities for continuous improvement through audit findings and quality metrics.
- Drive corrective and preventive actions (CAPA), ensuring timely implementation and effectiveness verification.
- Serve as the primary quality representative during customer, regulatory, certification, and government agency audits.
- Ensure compliance with FDA regulations, ISO standards, customer requirements, and internal quality procedures.
- Partner with Manufacturing, Engineering, Regulatory Affairs, and Operations teams to implement quality system improvements.
- Develop and deliver training programs related to quality systems, regulatory requirements, and audit readiness.
- Mentor and develop quality personnel while promoting a culture of quality and continuous improvement.
- Maintain audit records and ensure compliance documentation is inspection-ready at all times. Required Qualifications
- Bachelor's degree in Engineering, Quality, Life Sciences, or another related technical discipline.
- Minimum
- 6 years of experience
- in Quality Systems, Quality Compliance, Quality Assurance, or Regulatory Compliance within a regulated manufacturing environment.
- Strong experience planning and leading internal quality system audits.
- Experience supporting customer, FDA, ISO, or third-party regulatory audits.
- Working knowledge of Quality Management Systems (QMS), CAPA, document control, and regulatory compliance.
- Excellent communication skills with the ability to influence cross-functional teams.
- Strong organizational skills with the ability to manage multiple priorities in a fast-paced manufacturing environment. Preferred Qualifications Experience working within one or more of the following quality standards:
ISO 13485
ISO 9001
- AS9100
IATF 16949 / ISO TS16949
- TL9000 Experience supporting medical device, pharmaceutical, aerospace, or other highly regulated manufacturing environments is strongly preferred.