Job Type: Full Time / On_site
Salary Range: $120,000 - $125,000 plus 6% bonus.
How You'll Make an ImpactAs 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 EnvironmentAt 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
- Comprehensive medical, dental & vision coverage
- Health Savings Account (HSA)
- Paid holidays, vacation, and parental leave
- Flexible work environment
- Learning and development opportunities
- Career and professional growth
- Inclusive culture and vibrant community engagement
Learn more at benefits.lubrizol.com!
#LI-LT1 #LBZUS
