Supplier Quality Engineer

Job Posting Start Date 07-22-2025 Job Posting End Date 09-22-2025

Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.

A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.

Job Summary

Farm, a Flex company with over 50 years of experience in providing award-winning development services for medical, life sciences, and consumer healthcare sectors, is seeking a Supplier Qualtiy Engineer in Hollis, NH.

The Supplier Quality Enginee r is responsible for supporting supplier-related activities on development teams at Farm. He or she ensures that the development team is compliant with the policies and procedures of Farm's quality management system (QMS). The Supplier Quality Engineer receives direction from the Director of Quality and input from Program Managers and program team members.

• Support product development as an embedded program team member working alongside program managers, researchers, human factors engineers, designers, mechanical engineers, electrical engineers and process engineers.
• Facilitate selection of suppliers to support late-stage development and clinical builds.
• Qualify suppliers via capability questionnaires, risk assessment, supplier file creation/management and remote or on-site audits.
• Represent program team supplier quality requirements during collaboration with procurement and supply chain resources.
• Develop program supplier and incoming inspection plans for late-stage development and clinical builds based on input from program managers, engineers, suppliers and customers.
• Plan and support test method and process validation activities completed by suppliers.
• Complete incoming inspection and management of materials for late-stage development and clinical builds.
• Manage site non-conforming material review process.
• Lead supplier-related corrective action and preventive action resolution.
• Manage site quality management system approved supplier list, supplier files and supplier performance metrics.
• Establish, evaluate, qualify, encourage use of and continuous improvement to supplier management processes, procedures and standard tools used by program teams.
• Participate in internal, customer and notified body audits of the quality management system.
• Interacts with customers, suppliers and external auditors to develop close working relationships.
• Participates in customer strategy meetings and discussions regarding the development of program quality requirements and plans.
• Participates in the technical review process on development programs.

• Bachelor's degree in engineering, science, or equivalent technical discipline
• 4+ years of supplier quality experience
• Analytical thinking, plus verbal and technical writing skills
• Demonstrated team collaboration experience
• Previous medical device industry experience/ ISO13485 (prefer)

• Full range of medical, dental, and vision plans
• Life Insurance
• Short-term and Long-term Disability
• Matching 401(k) Contributions
• Vacation and Paid Sick Time
• Tuition Reimbursement