Quality Engineer, Supplier Quality
US–CA–Irvine, Vacancy ID JR-4370

Integra LifeSciences is a global medical technology leader in neurosurgery and regenerative medicine driven by our purpose of restoring patients’ lives. The company offers a broad portfolio of products and innovative solutions for dural access and repair, cerebral spinal fluid management and neuro-critical care. Its regenerative tissue technologies include products that address soft tissue, peripheral nerve and tendon repairs and for the treatment of acute and chronic wounds, burns, as well as for plastic and reconstructive surgery.
Founded in 1989 by Richard E. Caruso, the company is headquartered in Princeton, New Jersey. Today, Integra LifeSciences has grown immensely, with more than 4200 employees worldwide as well as offices, manufacturing and research facilities in Asia, Australia, Europe, Middle East, and the Americas.
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Supplier Quality Engineer 1 is responsible for supporting the supplier quality management process. This includes ensuring that suppliers meet the company’s quality requirements, conducting audits, collaborating with suppliers on quality improvement initiatives, and helping resolve quality issues related to purchased components or services through Supplier Change Requests (SCR).
Key Responsibilities:
Supplier Quality Management:
Assist in monitoring and maintaining supplier performance related to product quality.
Conduct supplier quality assessments and audits to ensure compliance with company standards.
Work with suppliers to address quality concerns and provide recommendations for corrective actions.
Problem Solving and Root Cause Analysis:
Assist in investigating and resolving quality issues, including non-conformance, defects, and product failures.
Perform root cause analysis and contribute to corrective action planning with suppliers.
Supplier Development and Improvement:
Collaborate with suppliers to identify opportunities for quality and process improvements.
Assist in the implementation of quality improvement initiatives and cost-saving measures.
Quality Documentation and Reporting:
Support the preparation of supplier quality reports, tracking performance metrics, and presenting findings to management.
Assist in creating and maintaining quality records, including inspection reports, non-conformance reports, and corrective action plans.
Collaboration:
Work closely with internal teams such as Procurement, Engineering, and Manufacturing to ensure that quality standards are met throughout the supply chain.
Communicate supplier issues effectively to cross-functional teams, working to ensure a prompt resolution.
Compliance and Standards:
Ensure compliance with industry standards, regulatory requirements, and customer specifications.
Stay updated on the latest quality trends and industry regulations, applying this knowledge to improve supplier quality performance.
Supplier Qualification:
Assist in evaluating new suppliers for potential qualifications, including conducting audits, reviewing certifications, and assessing quality systems.
QUALIFICATIONS:
Bachelor’s degree in engineering, Quality, or related field.
Basic understanding of quality systems (ISO 9001, Six Sigma, etc.).
Strong problem-solving skills and ability to conduct root cause analysis.
Familiarity with statistical analysis and quality control tools (e.g., SPC, FMEA).
Excellent communication and interpersonal skills for dealing with both internal teams and external suppliers.
Ability to work collaboratively in a team-oriented environment.
Attention to detail and a commitment to continuous improvement.
Preferred Qualifications:
Some experience or internships in supplier quality, quality assurance or manufacturing environments.
Knowledge of quality tools such as 8D, FMEA, Control Plans, etc.
Familiarity with ERP systems (e.g., SAP, Oracle, Agile) and data analysis software.
Work Environment:
Office-based with occasional travel to supplier sites for audits, assessments, and meetings.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
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EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra – Employer Branding from Integra LifeSciences on Vimeo
We are proud of our 25 year heritage as a leader in regenerative medicine. Today, our scientific innovation and diverse product portfolio continue to help patients and surgeons around the world.
We have an entrepreneurial, small company feel, yet deliver big company results. Your ideas – big and small – are welcome here. We embrace change and reward our people who are committed to making Integra a stronger company.
We believe how we do things is as important as what we do. Our Values guide how we work and how we act towards our customers, patients and each other every day. We value Our People, Integrity, Excellence, Embracing Change, Decisiveness and Teamwork.