Demo

Quality Engineer

Valtronic
Solon, OH Full Time
POSTED ON 2/22/2025
AVAILABLE BEFORE 3/23/2025
Job Details

Job Location

Solon, OH

Description

ESSENTIAL FUNCTIONS:

  • Understanding of ISO 13485:2016 requirements, (e.g. FMEA, CAPA, Root Cause Corrective Action and Customer Feedback).
  • Create and maintain quality Metrics when assigned Execute design controls and analyzes design inputs.
  • Develop and implement Data Analysis metrics.
  • Leads investigations related to quality problems.
  • Ability to define and manage risk-management plan, risk assessment and risk-control tools.
  • Facilitate or independently lead non-conforming product investigations, including corrective/preventive actions and product remedial actions.
  • Responsible for systems assurance including documentation, testing and inspection, and product and process development.
  • Will support Manufacturing, New Product Development, and Regulatory (as applicable) to ensure systems are in compliance with internal and external guidelines and regulations.
  • Identify and lead product and systems continuous improvement initiatives.
  • Communicate effectively at all levels within Quality, as well as cross-functionally with R&D, Manufacturing, Supply Chain, Customer Service, Sales, and other functions as necessary.
  • Able to influence decisions in a cross-functional team setting.
  • Knowledge Equipment Qualification Experience (IQ/OQ/PQ).
  • May participate in internal/external audits.

QE-NPD Focus

  • Lead and support new product development execution of design control from concept through post-launch phases.
  • Support design change activities through product lifecycle.

Valtronic Technologies is an Equal Opportunity Employer

Qualifications

EDUCATION AND EXPERIENCE:

  • Higher education degree or 5 years work experience in lieu of degree.
  • Handle various projects and responsibilities simultaneously and successfully meet deadlines.
  • Microsoft Excel//Word, and PowerPoint. Work with other groups or individuals to resolve issues.
  • Medical Device experience required to include ISO 13845:2016 including Knowledge of
  • FDA regulations
  • Excellent written and oral communication skills.

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