Quality Engineer Vantedge Medical - 3.3 Rancho Cordova, CA Job Details Full-time $90,000 - $115,000 a year 8 hours ago Qualifications Defect resolution root cause analysis ISO standards Technical writing experience within manufacturing English Manufacturing standard operating procedures Medical device manufacturing facility experience Quality assurance standard operating procedures Biomedical regulatory compliance Standard operating procedures drafting Data analysis software

Full 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.