Senior Quality Manager

Overview

Lubrizol Corporation is hiring a Senior Quality Manager.

Location:

Corona, CA, US 92879. Job Type: On-Site / Full Time. Salary Range: $150,000 - $180,000 plus 15% bonus.

As a Senior Quality Manager
, you will be at the forefront of our innovation, ensuring that our Quality Systems meet Excellence standards, regulations, and internal requirements through the development, implementation, and monitoring of appropriate processes, people, tools, metrics, and goals. You will collaborate with a diverse group of professionals to deliver sustainable solutions to advance mobility, improve wellbeing, and enhance modern life.

• Drive development, implementation, and improvement in our Operation Quality Systems.
• Manage the Quality Engineering team and direct the activities of Quality Engineers, Quality Control Supervisor and Document Control Supervisor.
• Analyze Quality Systems data to identify and recommend actions to meet organizational Quality Systems and strategic objectives.
• Act as technical advisor on Quality Systems matters.
• Directly own internal/external audits and supplier controls.
• Establish goals and metrics related to people, processes and product for the Quality Engineering team.
• Provide input to the development of departmental performance objectives.
• Plan, promote, and organize training activities related to Quality Systems.
• Plan and develop the site-level Management Review.
• Drive product quality and compliance through the development, implementation, monitoring and improvement of site-level Quality Systems.
• Facilitate and respond to Supplier & Customer Surveys including but not limited to Quality System Surveys, REACH, RoHS, Latex, WEEE Compliance surveys, etc.
• Observe and promote Company standards and policies on safety, quality, and productivity.

• Bachelor's degree
• 10+ years of experience in Quality Management including both Quality Assurance and Quality Control
• 5+ years of experience managing people
• 5+ years of FDA Medical Device manufacturing experience
• Experience with ISO 14971 Medical Device Risk Management
• Experience with ISO 13485 at the mastery level and proficiency of FDA 21 CFR Part 820
• Experience with MS Office Products

• Quality
  
  Certifications:
  
  Six Sigma Black Belt or Green Belt
• Quality Audit Experience
• Customer Audit Experience
• Experience with EQMS and MSA
• Advanced Degree

• 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

• 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 community engagement

Nearest Major Market:
Corona
• Nearest Secondary Market:
Los Angeles