Job Description

Manufacturing Engineer

Location: Salt Lake City, UT

Duration: 18+ Month W2 Contract (No C2C Available)

Position Summary:

The Manufacturing Engineer is responsible for supporting and improving manufacturing operations with a focus on patient safety, product quality, and regulatory compliance. This role requires strong technical expertise, project management skills, and the ability to work both independently and collaboratively across functions.

Key Responsibilities:

• Collaborate effectively within cross-functional project teams.
• Perform complex statistical, geometric, and mathematical calculations.
• Work independently with minimal supervision.
• Read, understand, and create engineering drawings using common engineering software.
• Use personal computer hardware and software efficiently; proficient in Microsoft Office applications.
• Uphold a primary commitment to patient safety, product quality, and compliance with our client’s Quality Manual and regulatory standards.
• Document and improve manufacturing processes to ensure device safety and efficacy.
• Conduct qualification, verification, and validation activities for medical device production.
• Analyze, troubleshoot, and resolve safety, quality, cost, and delivery issues related to components and finished devices.
• Support new product development and product support through engineering activities, including technology development, process studies, process improvements, and report preparation.
• Develop manufacturing equipment compliant with OSHA, EPA, and other safety standards.
• Design, procure, and fabricate tooling and fixtures.
• Participate in design control efforts such as risk analysis (FMEA) and design reviews.
• Source and assess component and service suppliers (preferred).
• Train, develop, and provide work direction to operators and technicians.
• Identify, implement, and manage production goals and improvement initiatives.
• Coordinate, manage, and document project work, recommending revisions as necessary.
• Design and conduct engineering tests and experiments; analyze data and present results.
• Collaborate with production supervisors, product builders, and technicians to troubleshoot and resolve production issues.
• Attend and contribute to production core team meetings.

Preferred Qualifications:

• Experience with Six Sigma methodologies.
• Previous supplier sourcing and supplier management experience.
• Experience in a medical device manufacturing environment.

Skills and Competencies:

• Strong analytical and problem-solving skills.
• Excellent communication and documentation abilities.
• Ability to manage multiple projects and priorities in a dynamic environment.
• Commitment to quality, safety, and continuous improvement.

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