Quality Engineering Temp

Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. 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.

This Supplier Quality Engineer II role serves as a key quality representative supporting contract manufacturers and raw material suppliers involved in the production of Integra products. The position is responsible for supplier audits, supplier performance monitoring, CAPA and nonconformance management, supplier change control, quality agreement management, and validation activities while ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and other applicable regulatory requirements.

The ideal candidate will have experience working in a regulated medical device or life sciences environment and possess a strong understanding of supplier quality systems, root cause investigations, and quality engineering principles. This role partners closely with Quality Control, Manufacturing, Purchasing, and supplier organizations to drive continuous improvement, resolve quality issues, and ensure supplier compliance. It is an excellent opportunity for a quality professional looking to influence supplier performance, support business continuity, and contribute to the delivery of safe and effective medical products.

Provides quality assurance leadership to select contract manufacturing sites and raw material suppliers engaged in the production of Integra products

Conducts Supplier Audits according to good manufacturing practices, ISO Standards, and applicable regulatory requirements

Establish and ensure Supplier Quality Agreements are up to date for applicable suppliers engaged in the production of Integra products

Report on contract manufacturer performance metrics

Ensure technical support to QC, purchasing and production departments

Provide Quality Engineering Support to suppliers including audits/assessments, inspection technique support, verification /validation activities, CAPA and change management. Addresses Supplier Change Requests in compliance with procedures and regulatory requirements

Ensures that activities for validation of outsourced processes/products are performed and documented according to procedures and within the defined timeline

Ensures that Supplier Non-conformances are initiated, dispositioned, approved and investigated according to plans and in compliance with procedures and regulatory requirements

Escalate supplier quality issues to management as appropriate, develop and propose robust and compliant solutions

Manages or participates in quality projects as required

Provides support with complaint investigations as required

A minimum of a Bachelor’s Degree in an Engineering, Life Science, or a related technical discipline. Minimum 3 years of professional work experience in a GMP and /or ISO regulated industry.

Knowledge of Medical device standards and regulations such as ISO13485, 93/42 EEC, 21 CFR part 820.

Strong analytical problem solving and root cause analysis skills

Use of ERP, PLM systems

Use of Microsoft office tools

Experience working in a Medical Device or Life Science manufacturing environment.

Operations supplier quality experience, with a strong understanding of process validation (IQ, OQ, PQ).

Experience or knowledge with the machining processes, injection molding, and/or electro-mechanical components/assembly.

Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciences

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.

This site is governed solely by applicable U.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 View email address on click.appcast.io - Employer Branding from Integra LifeSciences on Vimeo

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