Noveon Magnetics Inc.
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Job Title: Quality Management System (QMS) Manager
Reports to:
Director of Quality
Location:
San Marcos, Texas
We have one goal: to manufacture quality magnets! We are looking for exceptional individuals who want to learn, build, and lay a foundation for our company for the years to come.
About This Role The Quality Management System (QMS) Manager is responsible for overseeing and maintaining the Company’s Quality Management System to ensure compliance with internal policies, regulatory requirements, and industry standards, including ISO 9001 and IATF 16949. This position will play a key role in assisting the Company in achieving IATF 16949 certification by ensuring systems, documentation, and processes meet the necessary requirements. The QMS Manager manages audits, document control, supplier quality, and company-wide quality compliance initiatives while working cross‑functionally with all departments to drive continuous improvement, operational excellence, and Lean Six Sigma initiatives.
What we have to offer
Competitive Base
Medical/Dental/Vision insurance on day 1 of employment
Health Saving Account (HSA) with Employer contribution
Employee Assistance Program
401(k) retirement plan and match program
Long Term Disability (Employer Paid)
Short Term Disability (Employer Paid)
Paid Time Off (eligible after 90 days of employment)
Sick Leave
Company Paid Holidays
Diversity At Noveon Magnetics, we believe our diversity makes us who we are, and we strive every day to build a culture where everyone feels welcome.
What you’ll be doing
Developing, implementing, and maintaining the Quality Management System (QMS) in accordance with ISO 9001, IATF 16949, and applicable regulatory or customer‑specific requirements.
Leading and supporting the Company’s initiative to maintain our AS9100 certification and achieving guide our systems toward IATF 16949, ensuring compliance readiness across all departments.
Overseeing internal, external, and supplier audit programs, including scheduling, conducting, documenting findings, and verifying corrective and preventive actions (CAPA).
Assisting and supporting external supplier QA audits, including preparation, documentation, and follow‑up of supplier corrective actions.
Coordinating and supporting customer audits, ensuring timely and accurate responses to findings and inquiries.
Managing the document control processes to ensure accuracy, accessibility, and version control of quality‑related documents and records.
Overseeing and maintaining the nonconformance process, ensuring issues are properly identified, documented, investigated, and resolved.
Leading and facilitating management reviews, preparing reports and data summaries related to audit results, performance metrics, and improvement opportunities.
Collaborating with department leaders to ensure training, process adherence, and documentation meet QMS and certification requirements.
Monitoring and analyzing quality metrics and dashboards to assess performance and identify areas for improvement.
Providing document control support to ensure timely updates and consistent use of approved procedures, forms, and work instructions.
Leading and participating in Lean Manufacturing and Six Sigma projects to reduce waste, improve process efficiency, and enhance product quality.
Driving continuous improvement initiatives to strengthen quality systems, increase productivity, and promote a culture of excellence.
Providing guidance, training, and support to employees and suppliers regarding QMS, IATF 16949, and quality best practices.
We are looking for someone who
Has a Bachelor’s degree in Quality Management, Engineering, or a related technical field (or equivalent experience).
Has 5+ years of experience in quality systems management or compliance, preferably in an automotive or manufacturing environment.
Can display a strong knowledge of ISO 9001 and a working knowledge of IATF 16949 standards, with the ability to guide the organization toward certification.
Possesses experience with internal, supplier, and customer audits and the nonconformance/CAPA process.
Has experience applying Lean Manufacturing and Six Sigma principles for process improvement and defect reduction.
Possesses excellent organizational, communication, and problem‑solving skills.
Is proficient with document control systems, QMS software, and Microsoft Office Suite.
Can work collaboratively across departments and with suppliers and customers.
Physical Requirements
Prolonged periods sitting at a desk and working on a computer.
Must be able to lift/move up to 15 pounds at times.
About Noveon Magnetics At Noveon Magnetics, we’re reimagining the rare earth magnet industry and changing the way we electrify the world. We’re a fast‑growing, diverse team of scientists, engineers, entrepreneurs, and innovators from across the globe united by a shared mission to support the commercialization of our magnet manufacturing technology and forge a new path toward resource efficiency, resource independence and a low‑carbon economy.
As the only U.S manufacturer of permanent rare earth magnets essential to a range of technologies that rely on an electric motor— from electric vehicles to medical devices to aerospace and defense systems to clean energy— we’re ushering in an electric future that is 100% Made in America. All our operations, from R&D through production, assembly, and delivery, are conducted out of our state‑of‑the‑art manufacturing center in San Marcos, Texas.
Noveon Magnetics is an Equal Opportunity Employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Manufacturing
#J-18808-Ljbffr
Job Title: Quality Management System (QMS) Manager
Reports to:
Director of Quality
Location:
San Marcos, Texas
We have one goal: to manufacture quality magnets! We are looking for exceptional individuals who want to learn, build, and lay a foundation for our company for the years to come.
About This Role The Quality Management System (QMS) Manager is responsible for overseeing and maintaining the Company’s Quality Management System to ensure compliance with internal policies, regulatory requirements, and industry standards, including ISO 9001 and IATF 16949. This position will play a key role in assisting the Company in achieving IATF 16949 certification by ensuring systems, documentation, and processes meet the necessary requirements. The QMS Manager manages audits, document control, supplier quality, and company-wide quality compliance initiatives while working cross‑functionally with all departments to drive continuous improvement, operational excellence, and Lean Six Sigma initiatives.
What we have to offer
Competitive Base
Medical/Dental/Vision insurance on day 1 of employment
Health Saving Account (HSA) with Employer contribution
Employee Assistance Program
401(k) retirement plan and match program
Long Term Disability (Employer Paid)
Short Term Disability (Employer Paid)
Paid Time Off (eligible after 90 days of employment)
Sick Leave
Company Paid Holidays
Diversity At Noveon Magnetics, we believe our diversity makes us who we are, and we strive every day to build a culture where everyone feels welcome.
What you’ll be doing
Developing, implementing, and maintaining the Quality Management System (QMS) in accordance with ISO 9001, IATF 16949, and applicable regulatory or customer‑specific requirements.
Leading and supporting the Company’s initiative to maintain our AS9100 certification and achieving guide our systems toward IATF 16949, ensuring compliance readiness across all departments.
Overseeing internal, external, and supplier audit programs, including scheduling, conducting, documenting findings, and verifying corrective and preventive actions (CAPA).
Assisting and supporting external supplier QA audits, including preparation, documentation, and follow‑up of supplier corrective actions.
Coordinating and supporting customer audits, ensuring timely and accurate responses to findings and inquiries.
Managing the document control processes to ensure accuracy, accessibility, and version control of quality‑related documents and records.
Overseeing and maintaining the nonconformance process, ensuring issues are properly identified, documented, investigated, and resolved.
Leading and facilitating management reviews, preparing reports and data summaries related to audit results, performance metrics, and improvement opportunities.
Collaborating with department leaders to ensure training, process adherence, and documentation meet QMS and certification requirements.
Monitoring and analyzing quality metrics and dashboards to assess performance and identify areas for improvement.
Providing document control support to ensure timely updates and consistent use of approved procedures, forms, and work instructions.
Leading and participating in Lean Manufacturing and Six Sigma projects to reduce waste, improve process efficiency, and enhance product quality.
Driving continuous improvement initiatives to strengthen quality systems, increase productivity, and promote a culture of excellence.
Providing guidance, training, and support to employees and suppliers regarding QMS, IATF 16949, and quality best practices.
We are looking for someone who
Has a Bachelor’s degree in Quality Management, Engineering, or a related technical field (or equivalent experience).
Has 5+ years of experience in quality systems management or compliance, preferably in an automotive or manufacturing environment.
Can display a strong knowledge of ISO 9001 and a working knowledge of IATF 16949 standards, with the ability to guide the organization toward certification.
Possesses experience with internal, supplier, and customer audits and the nonconformance/CAPA process.
Has experience applying Lean Manufacturing and Six Sigma principles for process improvement and defect reduction.
Possesses excellent organizational, communication, and problem‑solving skills.
Is proficient with document control systems, QMS software, and Microsoft Office Suite.
Can work collaboratively across departments and with suppliers and customers.
Physical Requirements
Prolonged periods sitting at a desk and working on a computer.
Must be able to lift/move up to 15 pounds at times.
About Noveon Magnetics At Noveon Magnetics, we’re reimagining the rare earth magnet industry and changing the way we electrify the world. We’re a fast‑growing, diverse team of scientists, engineers, entrepreneurs, and innovators from across the globe united by a shared mission to support the commercialization of our magnet manufacturing technology and forge a new path toward resource efficiency, resource independence and a low‑carbon economy.
As the only U.S manufacturer of permanent rare earth magnets essential to a range of technologies that rely on an electric motor— from electric vehicles to medical devices to aerospace and defense systems to clean energy— we’re ushering in an electric future that is 100% Made in America. All our operations, from R&D through production, assembly, and delivery, are conducted out of our state‑of‑the‑art manufacturing center in San Marcos, Texas.
Noveon Magnetics is an Equal Opportunity Employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Quality Assurance
Manufacturing
#J-18808-Ljbffr