Supplier Quality Engineer

Smith Nephew; Memphis (TN); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

401(k) Matching

Tuition Reimbursement

Discounted Stock Purchase Plan

Flexible work options

Job summary

Smith+Naphew in Memphis, Tennessee, is seeking a Supplier Quality Engineer to ensure supplier quality and regulatory compliance across our medical device operations. You will collaborate with Manufacturing Engineering, Quality, Operations, and suppliers worldwide to drive quality excellence and implement improvements.

The role requires 3+ years in supplier quality or related fields, familiarity with ISO 13485, SAP experience, and strong problem solving.

Qualifications

• Bachelor's degree in engineering required; 5+ years in supplier quality/regulated manufacturing.
• ISO 13485 knowledge and external audit exposure preferred.
• Experience managing nonconformances, CAPAs, supplier investigations, and quality system processes.
• Experience with calibration, CMM, gauging and measurement techniques is beneficial.

Responsibilities

• Support global supplier quality strategy and goals.
• Manage supplier nonconformances using SAP QNs and related systems.
• Lead CAPAs, supplier investigations, field actions and complaints.
• Collaborate with Manufacturing Eng, Quality Eng, Operations and suppliers to resolve issues.

Skills

Communication

Project management

Relationship building

Education

Bachelor's degree in Mechanical Engineering or Biomedical Engineering

Associates degree in engineering + 5 years of supplier quality experience

Tools

SAP

Windchill

Power BI

Minitab

Microsoft Office

MS Project

Visio

Job description

Supplier Quality Engineer

Memphis, TN: Hybrid - must be onsite 3 times per week

Life. Unlimited. At Smith+Naphew we design and manufacture technology that takes the limits off living.

Join Smith+Naphew as a Supplier Quality Engineer in Memphis, Tennessee, where you will play a critical role in ensuring supplier quality and compliance across our medical device operations. This is an exciting opportunity to partner with cross functional teams and suppliers worldwide, driving quality excellence, continuous improvement, and patient focused outcomes while supporting a global quality strategy.

What will you be doing?

• Support the execution of the global supplier quality strategy and achievement of annual performance goals.
• Manage supplier related nonconformances through SmartSolve and SAP Quality Notifications (QNs).
• Apply knowledge of calibration, CMM equipment, and measurement systems (Gauging) to support supplier quality activities.
• Lead and support Corrective and Preventive Actions (CAPAs), supplier investigations, field actions, and complaint activities.
• Collaborate closely with Manufacturing Engineering, Quality Engineering, Operations, and supplier partners to resolve quality issues and implement improvements.
• Maintain compliance with quality systems, regulatory requirements, and industry standards applicable to medical devices.
• Support Supplier Change Notification (SCN) activities and supplier qualification processes.
• Review, update, and maintain Supplier Quality Agreements (SQAs) and Supplier Quality Contracts (SQCs) where applicable.
• Participate in external audits including MDSAP, FDA, and other regulatory or certification audits.
• Utilize problem solving methodologies such as Lean A3, Six Sigma, and 8D to identify root causes and implement sustainable solutions.
• Support business initiatives, quality projects, reporting activities, and continuous improvement efforts across the organization.
• Apply knowledge of calibration, CMM equipment, and measurement systems to support supplier quality activities.
• Develop project plans, track progress, and communicate updates to stakeholders as needed.

What will you need to be successful?

• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related engineering discipline. Associates degree in engineering and 5 years of work experience in supplier quality engineering.
• Approximately 3+ years of experience in Supplier Quality, Quality Engineering, Manufacturing Engineering, or a related medical device or regulated manufacturing environment.
• Working knowledge of ISO 13485; ISO 19011 knowledge preferred.
• Experience managing nonconformances, CAPAs, supplier quality investigations, and quality system processes.
• Knowledge of calibration processes, CMM equipment, gaging systems, and quality measurement techniques.
• Proficiency with SAP, Windchill, Power BI, Minitab, Microsoft Office applications, MS Project, and Visio.
• Strong communication, project management, and relationship building skills with the ability to work independently and across global cross functional teams.
• Experience using structured problem solving tools including Lean A3, Six Sigma, and 8D methodologies.

You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.

Inclusion and Belonging : Committed to welcoming, celebrating and thriving on Inclusion and Belonging.

Your Future :

• 401(k) Matching Program
• 401(k) Plus Program
• Discounted Stock Purchase Plan
• Tuition Reimbursement

Work/Life Balance :

• Flexible Personal/Vacation Time Off
• Paid Holidays
• Flex Holidays
• Paid Community Service Day

Your Wellbeing :

• Medical
• Dental
• Vision
• Health Savings Account (Employer Contribution of $500+ annually)
• Employee Assistance Program
• Parental Leave
• Fertility and Adoption Assistance Program

Flexibility :

• Hybrid Work Model (for most professional roles).

Training :

• Hands On
• Team Customized
• Mentorship

Extra Perks :

• Discounts on fitness clubs
• travel and more

Stay connected and learn more about Smith+Naphew at www.smith-nephew.com/careers.

Smith+Naphew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.

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