QMS Supervisor

Lubrizol Corporation

Corona (CA)

On-site

USD 120,000 - 125,000

Full time

14 days+

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Benefits offered by this job

Competitive salary with performance‑dr
401(k) match + Age-Weighted Defined
Health Savings Account (HSA)
Paid holidays, vacation, and parental

Job summary

Lubrizol Corporation in Corona, CA seeks a Quality Management System Supervisor to lead site QMS activities, drive internal audits and management review programs, and ensure compliance with FDA 21 CFR 820, ISO 13485, ISO 9001, and ISO 45001.

You will manage audit programs, liaise with customers and external bodies, train staff, develop KPIs, and support continuous improvement as part of the site leadership team, with a competitive salary and bonus.

Qualifications

  • Bachelor's degree from an accredited university.
  • 5+ years experience leading a QMS within a regulated manufacturing industry, (medical devices preferred)
  • 5+ years of demonstrated leadership experience leading/managing cross-functional teams.
  • 5+ years of experience managing others.
  • Experience leading audit programs.
  • Experience as an internal and external liaison on quality needs.
  • Familiarity with the ISO 13485 and 21 CFR 820

Responsibilities

  • Be Responsible and accountable for all site QMS activities to be executed promptly and effectively.
  • Establish and sustain the site QMS in line with the required industry standards (e.g., FDA 21CFR 820, ISO13485, ISO14001 / ISO 9001 / ISO45001).
  • Lead and manage the audit program and ensure that all nonconformities raised during audits are effectively corrected and independently verified.
  • Lead and manage customer audits at the site.
  • Manage all external registration requirements to ensure they are met. Liaise with external entities on all matters relating to registration.
  • Ensure training for the Quality Management System is effective.
  • Ensure internal audits of the QMS are process-based per the audit plan and that they are effective.
  • Develop, implement, and manage key leading / lagging performance indicators (KPIs) related to the QMS.
  • Ensure all required inputs for the Management Review Meeting (MRM) are reviewed/assessed.
  • Work as part of the Management team to share ideas and improve operation, recommending, supporting, and implementing continuous improvement activities for the QMS.
  • Be responsible for the quality training program
  • Be accountable to conform and comply with all HSES policies and procedures.

Skills

QMS leadership
Cross-functional leadership
Audit programs
Internal/external liaison
ISO 13485 familiarity
21 CFR 820 familiarity

Education

Bachelor's degree

Job description

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Shape the Future with Us. At Lubrizol, we’re transforming the Specialty Chemical and Medical Solutions industries through science, sustainability, and a culture of inclusion. As part of our global team, you’ll be empowered to make a real impact—on your career, your community, and the world around you.

Job Type: Full Time / On_site

Salary Range: $120,000 - $125,000 plus 6% bonus.

How You’ll Make an Impact

As a Quality Management System Supervisor, you'll be at the forefront of our innovation and excellence by driving Quality Management Systems Activities, including internal audits and management review programs. You'll collaborate with a diverse group of passionate individuals to deliver sustainable solutions to advance mobility, improve wellbeing, and enhance modern life. In this role, you will:

  • Be Responsible and accountable for all site QMS activities to be executed promptly and effectively.
  • Establish and sustain the site QMS in line with the required industry standards (e.g., FDA 21CFR 820, ISO13485, ISO14001 / ISO 9001 / ISO45001).
  • Lead and manage the audit program and ensure that all nonconformities raised during audits are effectively corrected and independently verified.
  • Lead and manage customer audits at the site.
  • Manage all external registration requirements to ensure they are met. Liaise with external entities on all matters relating to registration.
  • Ensure training for the Quality Management System is effective.
  • Ensure internal audits of the QMS are process-based per the audit plan and that they are effective.
  • Develop, implement, and manage key leading / lagging performance indicators (KPIs) related to the QMS.
  • Ensure all required inputs for the Management Review Meeting (MRM) are reviewed/assessed.
  • Work as part of the Management team to share ideas and improve operation, recommending, supporting, and implementing continuous improvement activities for the QMS.
  • Be responsible for the quality training program
  • Be accountable to conform and comply with all HSES policies and procedures.
Required Qualifications that Enables Your Success
  • Bachelor's degree from an accredited university.
  • 5+ years experience leading a QMS within a regulated manufacturing industry, (medical devices preferred)
  • 5+ years of demonstrated leadership experience leading/managing cross-functional teams.
  • 5+ years of experience managing others.
  • Experience leading audit programs.
  • Experience as an internal and external liaison on quality needs.
  • Familiarity with the ISO 13485 and 21 CFR 820
Your Work Environment

At Lubrizol, we’re committed to providing a safe, inclusive, and empowering environment where you can do your best work—whether in a lab, on the production floor, or in a hybrid office setting. Depending on your role, your work environment may include:

  • Standing, walking, or operating equipment for extended periods
  • Working in a lab or manufacturing setting with appropriate PPE provided
  • Use of computers and digital tools in an office or hybrid environment
  • Occasional lifting or movement of materials
  • Adherence to rigorous safety protocols and ergonomic standards
  • [add site/role specific]

We continuously invest in our facilities and technologies to ensure they support your well-being, productivity, and growth. If you require reasonable accommodation, we are committed to working with you to ensure an inclusive and accessible experience.

Benefits that Empower You
  • Competitive salary with performance-based bonus plans
  • 401(k) match + Age-Weighted Defined Contribution
  • Health Savings Account (HSA)
  • Paid holidays, vacation, and parental leave

Lubrizol: Imagined for Life. Enabled by Science. Delivered by You. For nearly 100 years, The Lubrizol Corporation, a Berkshire Hathaway company, has been at the forefront of innovation to enhance everyday life, advance mobility, and make the modern world work better. Our specialty chemistry solutions—from engine oils, performance coatings, and skincare to medical devices and plumbing systems —are powered by the expertise, passion, and commitment of people like you. We tackle the world’s toughest challenges with science-based solutions, deeply understanding our customers to deliver innovative chemistry and differentiated value. Our inclusive culture, dedication to safety, and incredible global talent drive our success. Our solutions meet the evolving needs of the modern world—brought to life by science and, most importantly, delivered by you. Whether you're in the lab, on the production floor, or in the office, you'll be part of a team around the world that empowers you to think boldly, drive results, and contribute to solutions that shape a better, more sustainable future. We win because of you. Let’s build the future together.


Nearest Major Market: Corona
Nearest Secondary Market: Los Angeles
Job Segment: Chemical Research, Manager, Plumbing, Business Process, Quality Manager, Engineering, Management, Manufacturing, Quality

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