Quality Engineer

Vantedge Medical Company; Rancho Cordova (CA); On-site; USD 90,000 - 115,000; Full time

Job summary

Vantedge Medical Company is seeking a Quality Engineer for a full-time, onsite role in the United States. The candidate will support product and process quality activities, drive improvements, and ensure ISO 13485 compliance within a medical device manufacturing environment.

Responsibilities include CAPA analyses, supplier quality collaboration, and development of validation protocols while maintaining quality metrics across production.

Qualifications

• 4-year degree in Quality/Mechanical/Industrial engineering or related
• Experience in medical device/manufacturing quality environments preferred
• Strong knowledge of quality tools and problem solving methods

Responsibilities

• Generate internal quality reports based on CAPA, complaints and yield.
• Propose and drive product/process improvement initiatives.
• Work with suppliers and Supply Chain to improve performance.
• Maintain metrics to evaluate process performance with manufacturing.
• Coordinate PPQP activities (pFMEA, CP, Capability reports, GR&R).
• Assist the Director of Quality in maintaining ISO 13485 QMS.
• Create/Update work instructions and procedures as needed.
• Lead and/or create equipment validation protocols and reports.

Skills

Quality problem solving

CAPA management

Statistical analysis

Education

4-year degree in Quality/Mechanical/Industrial engineering

Tools

Minitab

JMP

Job description

Description

Quality Engineer
Full-time | Permanent | Onsite

Salaried | $90k - $115k

*We are not accepting candidates from third party agencies.

About Us:
Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do – and have a lot of fun doing it.

About this Opportunity:
The Quality Engineer will provide support for product/process quality activities within Vantedge Medical. Areas of assignment may include: Product/Process improvement efforts, equipment validations, supplier quality performance and quality systems support.

Responsibilities:

• Generate internal quality reports based on CAPA, complaints and yield. Propose and drive product/process improvement initiatives.
• Work with suppliers and Supply Chain department to improve overall performance.
• Maintain metrics to evaluate process performance and work with manufacturing to ensure that expectations are met.
• Coordinate PPQP activities (pFMEA, CP, Capability reports, GR&R etc.).
• Assist the Director of Quality in maintaining ISO 13485 QMS.
• Create/Update work instructions and procedures as needed.
• Lead and/or create equipment validation protocols and reports.
• Undertake additional responsibilities or activities as required by Director of Quality.

Requirements

• 4-year degree in Quality/Mechanical/Industrial engineering or a closely related field.
• A minimum of 2 years of work experience in a related field in a medical device or manufacturing environment.
• Understand in depth quality systems, ISO 13485 and/or 9001 standards.
• Ability to create, review, and revise operating procedures, work instructions in English.
• Specific training and demonstrated success in applying quality problem solving method, such as fishbone diagrams, 5 why, FMEA, process capability analysis, hypothesis testing, DoE, SPC, etc.
• Minitab, JMP or other statistical software capabilities.