Quality Management System Supervisor

Job Title : Quality Management System Supervisor
Salary Range: $120-125K with a 6% bonus.
Location: Corona, CA
The role is 100% on-site and the client prefers candidates from California.

About the job
Shape the Future with Us. 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.

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

Role

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

Interested candidates send your resume to alex@amtexenterprises.com