Quality Engineer -Medical device – Aequor

Company: Aequor

Location: Irvine, CA

Salary: Not specified

Employment Type: Contract

Seniority Level: Associate

Applicants: 45

Apply on LinkedIn

Job Description

Job Title: Quality Engineer I

Location: Irvine CA onsite

Contract Length: 18 months with possible extension

Job Description:

The Quality Engineer is responsible for maintaining quality and control of manufacturing processes and post-market performance of medical devices. Responsibilities include collaborating with internal and external stakeholders to achieve company objectives, leading technical root cause investigations, developing and executing risk-based decisions, resolving and documenting customer complaint and manufacturing investigations, and representing Quality in cross-functional projects.

Job Duties:

  • Develops and executes plans for quality and control to ensure manufacturing continuity and product conformance.
  • Leads investigations into production and customer-facing quality issues to identify root cause, implement corrective and preventative actions, and monitor effectiveness
  • Monitors and analyses product performance of medical devices using a statistical and risk-based approach. Considers any quality, compliance, customer, and business risks.
  • Performs hands-on troubleshooting of customer returned devices and manufacturing nonconformities and completes associated technical documentation
  • Develops tools to communicate complex technical problems and solutions to a variety of audiences within the organization
  • Proficient in project management, data analysis, root cause analysis, communication, and risk determination
  • Ensure compliance with the company’s Quality System policies and procedures and applicable external requirements and standards, including FDA, ISO 13485, and other worldwide regulatory agencies as pertaining to medical devices.

Minimum Requirements:

  • Bachelor’s degree in Engineering
  • 3 years of relevant experience in a regulated industry (FDA environment preferred)
  • Knowledgeable of FDA regulations, 21 CFR part 820 and Part 803 and ISO 13485 standard
  • Strong verbal / written communication, with the ability to work effectively in cross-functional teams
Disclaimer: This job listing is sourced from LinkedIn and is provided for informational purposes. Apply directly through the employer’s application process. Medical Device Navigator is not affiliated with the hiring company.
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