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Quality Engineer

The Lubrizol Corporation · Corona, CA4w ago
$115k – $120kfrom the posting

BS-level Quality / Testing roles on Crosslinked list a median of $109k (164 that show pay).

Develop and implement quality assurance controls for medical devices, including validation, CAPA, and risk analysis.

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Worth knowing

Why it is interesting. Ensure compliance with ISO 13485 and FDA regulations in a hands-on quality role at a Berkshire Hathaway company.

Might not be for you. Heavy focus on documentation and compliance, less open-ended R&D.

Bench and deskDeep specialistMethodical pace BS acceptable

Adjacent materials roleLubrizol's Quality Engineers ensure our corporate quality standards and compliance to ISO 13485, CFR Title 21 Part 820, ISO 14971...

Seniority
Mid-level
Work
On-site
Type
Full-time
Degree
BS
Experience
2+ yrs
Industry
Medical devices
Role
Quality / Testing
Schedule
Standard
Benefits
401(k) match + Age-Weighted Defined Contributionparental leaveflexible work environment

Role details

*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

$115,000 - $120,000 with 6% bonus target

How You’ll Make An Impact

Lubrizol’s Quality Engineers ensure our corporate quality standards and compliance to ISO 13485, CFR Title 21 Part 820, ISO 14971 and other applicable standards. Our QEs provide product engineering support but assessing risk, analyzing process capabilities, and finally, developing and implementing effective quality assurance controls. Our QEs have a “hands-on” approach to problem solving, problem investigation and data mining. In this role, you will:

  • Develop, write, and drive effective quality assurance controls
  • Write validation and verification plans and protocols, and assist with IQ/OQ/PQ activities, including finalize reports.
  • Assist in process and/or product improvement projects.
  • Report, analyze and coordinate the resolution of material nonconformance occurrences.
  • Analyze data using statistical and quality tools and perform thorough Root Cause Analysis (e.g., Fishbone Diagram, 6M, 5Whys).
  • Drive CAPA processes and improve process capabilities (e.g.,5S, Lean, 6 Sigma, DOE, SPC).
  • Conduct risk analysis and create, or revise, Control Plans for new and existing products.
  • Provide support in the rapid resolution of product complaints and/or safety issues.
  • Provide quality assurance appraisal of suppliers.
  • Conduct quality process and product audits and develop responsive corrective action plans.
  • Support completion of Customer requests (e.g., Supplier surveys, EU MDR compliance Declarations, etc.).
  • Provide support for operational quality management system programs

Required Qualifications That Enables Your Success

  • Bachelor’s Degree
  • 2 + years of experience in manufacturing, engineering or quality in an industrial setting.
  • Experience in medical device industry.
  • Experience and familiarity with tools for root cause analysis and defect analysis, including Failure Mode and Effect Analysis (FMEA).
  • Experience with developing and implementing process controls, corrective and preventive action (CAPA), that drive quality improvement.
  • Experience with Design of Experiments(DOE), process analysis, capability assessments.
  • Experience with verification and validation activities.
  • Able to develop and establish Control Plans, FMEAs, PPAPs.
  • Experience with Statistical Process Control (SPC) methods and analysis utilizing statistical software and visualization tools like Minitab, JMP or Statgraphics.
  • Familiarity with test methods validations or measurement systems analysis, test and inspection equipment, and valid acceptance sampling plans.
  • Experience with quality management systems.
  • Experience with Lean, or Six Sigma manufacturing principles

Preferred Qualifications That Drive You Forward

  • Bachelors degree in Engineering or other Technical Discipline
  • American Society for Quality Certifications: ASQ, CQE, CQA etc.
  • Six Sigma certification: Green Belt, Black Belt etc.
  • Experience with FMEA, 5 Why Analysis, Fishbone Diagrams, Fault Tree Analysis, and statistical analysis.

Your Work Environment

Role

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

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!

#LBZUS

Lubrizol: Imagined for Life. Enabled by Science. ™ Delivered by You. For nearly 100 years, The Lubrizol Corporation, a Berkshire Hathaway company, has been at the forefront of innovation to enhance everyday life, advance mobility, and make the modern world work better. Our specialty chemistry solutions—from engine oils, performance coatings, and skincare to medical devices and plumbing systems —are powered by the expertise, passion, and commitment of people like you.

We tackle the world’s toughest challenges with science-based solutions, deeply understanding our customers to deliver innovative chemistry and differentiated value. Our inclusive culture, dedication to safety, and incredible global talent drive our success. Our solutions meet the evolving needs of the modern world—brought to life by science and, most importantly, delivered by you.

Whether you're in the lab, on the production floor, or in the office, you'll be part of a team around the world that empowers you to think boldly, drive results, and contribute to solutions that shape a better, more sustainable future.

We win because of you. Let’s build the future together.

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Common questions

What is the salary for the Quality Engineer role at The Lubrizol Corporation?

The listed annual base salary range is $115K–$120K. This figure is taken from the posting itself.

Does The Lubrizol Corporation sponsor H-1B visas?

The Lubrizol Corporation has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the Quality Engineer role. Confirm with the employer before applying if visa support is required.

Where is the Quality Engineer role at The Lubrizol Corporation based?

This role is based in Corona, CA.

What degree is required for the Quality Engineer role at The Lubrizol Corporation?

This role requires a BS.

How many years of experience does this Quality Engineer role require?

The posting calls for at least 2 years of relevant experience.

What techniques or methods are required for this Quality Engineer role?

FMEA, CAPA, DOE, SPC, Root Cause Analysis.