Quality Engineer

Posted 21 Days Ago
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Rancho Cordova, CA, USA
In-Office
90K-115K Annually
Junior
Robotics • Industrial • Manufacturing
The Role
Supports product and process quality in a medical device manufacturing environment. Responsibilities include quality reporting, CAPA and complaint analysis, process improvement, supplier performance, manufacturing metrics, PPQP coordination, ISO 13485 quality system support, procedure development, and equipment validation. The role requires applying structured problem-solving and statistical methods using tools such as FMEA, SPC, process capability analysis, hypothesis testing, DOE, Minitab, or JMP.
Summary Generated by Built In

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.

Skills Required

  • Four-year degree in Quality, Mechanical, Industrial Engineering, or a closely related field
  • At least 2 years of related work experience in a medical device or manufacturing environment
  • In-depth understanding of quality systems and ISO 13485 and/or ISO 9001 standards
  • Ability to create, review, and revise operating procedures and work instructions in English
  • Training and demonstrated success applying quality problem-solving methods, including fishbone diagrams, 5 Whys, FMEA, process capability analysis, hypothesis testing, DOE, and SPC
  • Capability with Minitab, JMP, or other statistical software
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The Company
HQ: San Jose, CA

What We Do

Vantedge Medical is a leading partner for Medical Technology OEMs, specializing in precision metal manufacturing. They deliver end-to-end metals expertise from concept to full-scale production for medical devices, serving markets such as robotic assisted surgery, surgical instruments, and orthopedics.

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