Supplier Quality Assurance Engineer II — Medical Device (Hybrid — Arden Hills, MN) Contract

Job Description

Our Fortune 500 Medical Device client has an exciting opportunity for a Supplier Quality Assurance Engineer II.

Job Summary :

The Arden Hills Supplier Quality Engineering team is looking for high-energy, driven, passionate people!

The Supplier QA Engineer II will play a key part in leading performance improvement of suppliers and increasing the suppliers’ capabilities to consistently meet internal requirements. This role collaborates with cross-functional teams to address and resolve all component-related challenges throughout the supply chain. Additionally, the Supplier QA Engineer will support Global Sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects.

Responsibilities :

Drives improvement and corrective actions in the quality of components sourced from outside suppliers.

Assess & drive reactive as well as proactive supplier project(s) / investigations partnering with Supplier Engineering, Manufacturing / Test operations, Commercial Sourcing, Design Assurance, R&D

Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors. Exercises authority and judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Has a broad knowledge of a variety of alternatives and their impact on the business unit

Plans and organizes non-routine tasks with approval. Initiates or maintains work schedule and priorities. Plans and organizes project assignments and maintains project schedules

Works under general direction regarding the direction and progress of projects and special assignments. Independently determines and develops approach to solutions. Interprets, executes and recommends modifications to company policies. Assists in establishing departmental policies and procedures. Work is reviewed upon completion for adequacy in meeting objectives

Establishes and cultivates a wide range of business relationships to facilitate completion of assignments. Interacts with suppliers. Participates in determining goals and objectives for projects. May lead projects within the function or department and / or represents a specialized field in larger project teams. Influences middle management on business solutions

Contributes to the completion of specific programs and projects. Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources

In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality Systems

Required Qualifications :

BS degree in an Engineering related field, such as : Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 2-3 years related experience.

Experience in Quality Management Systems, regulatory compliance, and risk management.

Experience with problem solving quality tools, Corrective / Preventive Actions (CAPA), Technical Documentation

Preferred Qualifications :

Experience with or lead auditor certification to ISO13485, 9001, TS16949 standards

Ability to communicate cross functionally with suppliers, team members and leadership

Highly organized and detail-oriented with ability to manage multiple projects and prioritize effectively

Quality Systems Duties and Responsibilities :

Build Quality into all aspects of their work by maintaining compliance to all quality requirements.

Other Details :

Schedule : 08 : 00 : AM - 04 : 30 : PM

Work Setup : Hybrid - 3 days onsite in Arden Hills, MN

Contract Length : 9 Months (10 / 27 / 2025 - 7 / 26 / 2026)

Requirements

BS degree in an Engineering related field, such as : Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 2-3 years related experience. Experience in Quality Management Systems, regulatory compliance, and risk management. Experience with problem solving quality tools, Corrective / Preventive Actions (CAPA), Technical Documentation