Quality Systems Engineer

Job Description

TTI Consumer Power Tools, Inc., has an opening in its Anderson, SC corporate office for a Quality Systems Engineer
. The Quality Systems Engineer is responsible for maintaining and improving the company’s Quality Management System (QMS) to ensure compliance with ISO standards, regulatory requirements, and internal policies. This role manages document control systems (Master Control and SharePoint), supports audits, drives continuous improvement initiatives through data analysis and reporting, and partners cross-functionally to strengthen quality processes across the organization.

We offer competitive wages and a comprehensive benefits package — tuition assistance, 401(k), medical/dental/vision coverage, vacation, and holidays.

• Maintain and enhance the QMS in compliance with ISO 9001 and applicable regulatory standards.
• Support alignment toward a globalized quality system across facilities within the organization.
• Conduct internal audits and lead corrective and preventive actions (CAPA).
• Prepare for and support external audits by customers and regulatory bodies.

• Administer Master Control and SharePoint systems, including document control, change management, and training records.
• Manage the full document lifecycle (creation, revision, approval, distribution, archival).
• Ensure timely review, approval, and accessibility of controlled documents.

• Analyze quality data and trends to identify improvement opportunities.
• Lead quality system improvement projects and promote best practices.
• Prepare and present quality metrics and reports to leadership.

• Develop and deliver training on QMS processes, regulatory standards, and system tools.
• Provide ongoing guidance to teams on quality and compliance requirements.
• Develop the PDP (Product Development Process) with various departments and provide training in the same.

• Bachelor’s degree in Quality, Engineering, Life Sciences, or related field preferred.
• 10+ years of experience in quality systems within a regulated industry (manufacturing, medical device, pharmaceutical, etc.).

• Strong knowledge of ISO 9001 (ISO 13485 a plus).
• Experience with Master Control preferred.
• Strong SharePoint administration and development skills.
• Proficient in document management systems and change control processes.
• Excellent analytical, organizational, and project management skills.
• Strong communication and interpersonal abilities.

• CQA, CQE, ISO 9001 Lead Auditor, or similar quality certification.

• Primarily office-based with occasional time in production or lab environments.
• Limited travel for audits or training as needed.

• Competitive compensation and benefits package
• Health, dental, and vision insurance
• 401(k) with company match
• Professional development opportunities