QMS Supervisor
Lubrizol Corporation, Corona, CA, United States
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, ISO 13485, ISO 14001 / ISO 9001 / ISO 45001).
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 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 operations, 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 ISO 13485 and 21 CFR 820.
Your Work Environment
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.
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.
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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, ISO 13485, ISO 14001 / ISO 9001 / ISO 45001).
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 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 operations, 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 ISO 13485 and 21 CFR 820.
Your Work Environment
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.
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.
#J-18808-Ljbffr