Quality Engineer

Vantedge Medical

$90K — $115K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 4-year degree in Quality/Mechanical/Industrial engineering or related field
  • Minimum 2 years experience in a medical device or manufacturing environment
  • In-depth understanding of quality systems, ISO 13485 and/or 9001 standards
  • Proficient in creating and revising operating procedures and work instructions
  • Trained in quality problem-solving methods like FMEA and SPC
  • Experience with statistical software such as Minitab or JMP

Responsibilities

  • Generate internal quality reports and propose product/process improvements
  • Collaborate with suppliers and Supply Chain to enhance quality performance
  • Maintain performance metrics and ensure manufacturing expectations are met
  • Coordinate PPQP activities including pFMEA and Capability reports
  • Assist in maintaining ISO 13485 Quality Management System
  • Create and update work instructions and procedures
  • Lead creation of equipment validation protocols and reports

Benefits

  • Full-time, permanent position
  • Onsite work environment
  • Opportunity to contribute to quality system improvements in the medical device industry
  • Engagement in a range of quality assurance activities and methodologies
Full Job Description
Job Type

Full-time

Description

Quality Engineer
Full-time | Permanent | Onsite

Salaried | $90k - $115k

*We are not accepting candidates from third party agencies.

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.


Salary Description

$88.2 - $95.6

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