NSI P1 Quality Systems Manager

NSI P1 Quality Systems Manager Northern Stamping Inc Cuyahoga Heights, OH Job Details Full-time $110,000 - $130,000 a year 19 hours ago Qualifications Quality control corrective actions Performance dashboard reports Statistics Record keeping Document review (document control) Management Business intelligence Auditors team management

IATF 16949

2016 Six Sigma Green Belt Audit engagement planning 5 years Writing skills Engineering Supplier quality engineering practices Regulatory compliance Statistical Process Control Compliance audits & assessments Six Sigma methodology implementation Data reporting Corrective and preventive actions (CAPA) Quality management Compliance management implementation Bachelor's degree in engineering Bachelor's degree Data management Quality control documentation Certified Quality Auditor Mentoring Auditing experience within manufacturing industry Document archiving Quality assurance within automotive industry Lean Six Sigma Green Belt Continuous quality improvement (CQI) Manufacturing Root cause analysis Senior level Training Cross-functional collaboration Leadership Manufacturing company experience Communication skills Certified Quality Engineer Cross-functional communication Supply chain collaboration Excel data analysis Stakeholder management Full Job Description Position Summary The Manufacturing IATF Quality Systems Manager leads the design, implementation, maintenance, and continuous improvement of the site Quality Management System (QMS) to ensure compliance with applicable requirements and to drive measurable improvements in product quality, customer satisfaction, and operational performance. This role serves as the site subject-matter expert for quality systems, internal/external audits, and quality risk management, and partners closely with Manufacturing, Engineering, Supply Chain, and Customer Quality. The position reports to the Site Quality Director/Manager Key Responsibilities Own and continuously improve the site QMS, including governance, procedures, and process performance monitoring. Ensure effective document control, including creation, review, approval, revision control, archival, and timely obsolescence of controlled documents. Lead the internal audit program (risk-based schedule, auditor qualification, execution, reporting, and follow-up) and ensure readiness for customer, regulatory, and certification audits. Coordinate and host external audits/assessments; develop audit plans, manage logistics, and ensure timely, sustainable responses to findings. Own the Corrective and Preventive Action (CAPA) system: drive root cause analysis, effectiveness checks, and closure discipline; trend issues to prevent recurrence. Administer change control to ensure product/process changes are assessed, approved, verified/validated as required, and communicated prior to implementation. Manage nonconformance control processes (material review board support, disposition controls, containment, and systemic action linkage to CAPA). Lead Management Review activities and quality performance reporting; define and track key metrics (e.g., audit performance, CAPA cycle time, customer complaints, scrap/rework, first-pass yield). Helps in developing the site training system (competency requirements, training matrices, records, and effectiveness) to ensure workforce compliance. Partner with Manufacturing and Engineering to implement robust process controls, standard work, error-proofing, and continuous improvement initiatives. Support supplier quality system interfaces as applicable (e.g., supplier corrective actions, quality agreements, audits) in collaboration with Supply Chain and Supplier Quality. Drive quality culture through coaching, facilitation, and cross-functional problem-solving; mentor and develop quality systems staff and internal auditors. Ensure data integrity and effective use of electronic QMS tools (eQMS) and reporting dashboards; maintain accurate records and retention practices. Maintain awareness of applicable standards and customer-specific requirements; translate requirements into practical, scalable site processes. Required Qualifications Bachelor's degree in Engineering, Quality, Manufacturing, or a related field (or equivalent combination of education and experience). 5+ years of progressive quality experience in a manufacturing environment, including ownership of one or more core quality systems (e.g., audits, CAPA, document control, change control). Working knowledge of ISO 9001 and

IATF 16949

where applicable. Demonstrated experience leading internal and external audits and managing audit findings to closure. Proficiency with root cause analysis and problem-solving methodologies (e.g., 5 Whys, Ishikawa/Fishbone, 8D, A3). Strong data analysis and reporting skills (Excel and/or BI tools); ability to build meaningful metrics and drive actions from trends. Excellent written and verbal communication skills, including procedure writing and executive-level summaries. Ability to lead cross-functional teams, influence without authority, and manage multiple priorities with strong attention to detail. Preferred Qualifications Lead Auditor certification (ISO 9001 or applicable standard) and/or ASQ certification (e.g., CQE, CQA, CMQ/OE). Experience with automotive and/or manufacturing sector requirements (e.g., Hands-on experience implementing or administering an electronic QMS (eQMS) platform. Lean/Six Sigma background (Green Belt/Black Belt) with demonstrated continuous improvement results. Experience with statistical methods (SPC), measurement systems concepts, and process capability reporting. Prior people leadership experience (direct or dotted-line leadership of auditors/quality systems staff). Core Competencies Quality systems leadership and governance Risk-based thinking and practical problem solving Process approach and continuous improvement mindset Customer focus and strong follow-through Change leadership and stakeholder management Clear, structured communication and training effectiveness High integrity, confidentiality, and sound judgment Work Environment & Physical Demands Work is performed in a combination of office and manufacturing/warehouse environments. Position requires regular time on the production floor, including adherence to all safety rules and use of required personal protective equipment (PPE). May require occasional travel to support supplier, customer, or multi-site audits and meetings. Physical demands may include standing/walking for extended periods, bending, and lifting up to 25 lbs with or without reasonable accommodation. Equal Opportunity Employer We are an equal opportunity employer and are committed to creating an inclusive environment for all employees. Employment decisions are based on business needs, job requirements, and individual qualifications, without regard to any status protected by applicable law.