QMS Supervisor

QMS Supervisor

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 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