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# Quality Systems Specialist - Manufacturing - Shirley, MA

- **Company:** Page Michael International Inc
- **Location:** Ayer, MA, United States
- **Salary:** $83,000.0
- **Contract:** Permanent contract
- **Skills:** Document Management Systems, Software Version Control
- **Published:** June 17, 2026
- **Apply:** https://www.michaelpage.com/job-detail/quality-systems-specialist-manufacturing-shirley-ma/ref/jn-062026-7036018

## About the Role

* Experience within quality systems in a manufacturing environment
 * Strong background in ISO-compliant QMS implementation, maintenance, or auditing
 * Bachelor's degree in Engineering, Life Sciences, Quality, or related field
 * Formal internal or lead auditor certification/training
 * Deep knowledge of QMS elements (CAPA, document control, risk, supplier quality, etc.)
 * Excellent written and technical documentation skills
 * Ability to interpret regulations and translate into practical procedures
 * Strong analytical, organizational, and problem-solving capabilities
 * Proven ability to influence and challenge stakeholders constructively
 * Ability to work independently while leading cross-functional initiatives

## Description

This role leads and governs a site-wide Quality Management System, ensuring full compliance with ISO standards and regulatory expectations. You'll own internal audits, drive continuous improvement, and serve as the on-site expert for quality systems and audit readiness.

 * Lead ISO audits & shape QMS strategy at a global manufacturer
 * High-impact role with growth, autonomy, and cross-site influence, * Ensure the site QMS remains compliant with ISO standards, regulatory requirements, and corporate policies
 * Manage QMS documentation, maintaining structure, accuracy, and version control
 * Partner with cross-functional teams to align procedures with real-world operations and compliance needs
 * Develop and maintain quality manuals, process maps, and system frameworks
 * Own and execute the internal audit program, ensuring full annual coverage
 * Plan and perform system, process, and regulatory audits across departments
 * Evaluate audit evidence, identify nonconformities, and deliver detailed reports
 * Drive corrective action processes through to effective resolution
 * Train and mentor internal auditors as the program evolves
 * Conduct gap analyses and lead certification readiness efforts
 * Oversee key QMS elements (CAPA, training, supplier quality, risk, validation, etc.)
 * Support management reviews through performance metrics and compliance reporting
 * Partner with Quality Control to investigate system-level issues and root causes
 * Lead continuous improvement initiatives driven by audit findings and risk assessments
 * Deliver training on QMS processes, documentation practices, and audit readiness
 * Act as the site expert on ISO interpretation and quality system best practices
 * Supervise document control and training coordination resources


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