ABOUT CWT:

Custom Wire Technologies (CWT) is a leading OEM medical component manufacturer, with over 50 years of industry experience and implementation of the latest technology. Our services include custom wire coiling, wire coiling, custom grinding, wire forming, custom fine wire design, fine wire welding, laser processing, and manufacturing process validation.

We are a small, but growing family-owned and operated business. We are looking for a self-starter who has exceptional attention to detail, can adapt to changing priorities, and enjoys a dynamic work environment to fill the role of Quality Engineer.

JOB SUMMARY:

Under the direction of the Quality Manager, the Quality Engineer is responsible for the materials in-process and finished products, ensuring conformance to ISO 13485 and company quality standards, and customer specifications. Aides in the development of processes and standards to provide departmental efficiencies and enhance company profitability.

ROLES AND RESPONSIBILITIES:

• Develop, implement, and improve technical procedures related to quality control and product validation.
• Program and operate Vision System inspection machines.
• Lead and participate in validation activities (IQ, OQ, PQ) for equipment and new and existing products.
• Support the development and manufacturing of medical products, ensuring compliance with industry regulations.
• Provide leadership and guidance on quality assurance practices during the product lifecycle.
• Analyze quality data, identify problem areas, and assist in resolving manufacturing processes or methods that affect quality.
• Perform process capability studies; recommend changes to improve quality.
• Assist the organization in enforcing the Quality System and maintain consistent standards.
• Root cause analysis and implement corrective actions.
• Commit to the corporate goals, mission, and vision.
• Regular physical attendance is required.

QUALIFICATIONS:

• Bachelor of Science degree - Engineering required.
• 3+ years related quality experience in ISO manufacturing environment, med tech and ISO 13485 experience preferred.
• Strong knowledge and experience to perform validations and qualifications of products and processes.
• Ability to analyze and interpret blueprints.
• Proven experience with ability to manage multiple projects and meet deadlines.
• Strong problem-solving skills and ability to perform root cause analysis.

PREFERRED:

• ASQ quality certification
• Keyence, Micro Vu experience.
• Statistical background
• Experience working in a job shop manufacturing environment.

JOB HOURS:

The Position responsibilities would primarily occur during the core hours of 8 am to 5 pm, Monday through Friday. Manufacturing operates on three shifts and this position will occasionally require extended hours as needed. Infrequent Travel.

WORK ENVIRONMENT:

In-person manufacturing and office environment, climate controlled and mostly quiet.

Benefits:

We offer a comprehensive benefits package including:

• Medical
• Dental
• Vision
• Life and disability
• Paid Time Off
• 401(k) with company match
• Profit Sharing
• Paid Holidays