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Product Quality Engineer- Medical Device

Job in Atlanta, Fulton County, Georgia, 30383, USA
Listing for: Collabera
Full Time position
Listed on 2025-12-01
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 40 - 50 USD Hourly USD 40.00 50.00 HOUR
Job Description & How to Apply Below

Product Quality Engineer - Medical Device

This range is provided by Collabera. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$40.00/hr - $50.00/hr

Direct message the job poster from Collabera.

Position Overview

The Sr. Product Quality Engineer provides design quality expertise to product development teams, ensuring patient/user safety, customer satisfaction, and organizational success. This role involves leading risk management activities and supporting a broad range of development quality functions.

Key Responsibilities
  • Lead and support on-time completion of Design Control deliverables
  • Establish objective, measurable, and verifiable product requirements
  • Plan and execute Design Verification and Validation, including investigations and resolution activities
  • Lead risk management from product concept through commercialization
  • Support test method development and validation
  • Assist with manufacturing process development and qualification for new products and design changes
  • Define component specifications, sampling plans, and vendor qualifications
  • Support biocompatibility and sterilization qualifications
  • Participate in audits and quality system improvement initiatives
  • Support organizational initiatives in Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory compliance
  • Maintain collaborative communication with all levels of employees, contractors, and suppliers
Basic Qualifications
  • Bachelor’s degree in Engineering or related technical field
  • Minimum 5 years of experience in R&D, process/manufacturing engineering, or quality, with at least 2 years in product development
  • Experience in medical device regulations and standards
  • Experience in test method development and validation
  • Experience preparing risk assessments, FMEA, and other risk documentation
Preferred Qualifications
  • Advanced degree in Engineering or technical field
  • Experience with active implantable medical devices
  • Familiarity with requirements management tools (e.g., DOORS) and problem reporting systems (e.g., JIRA)
  • Working knowledge of statistics applied to verification and validation
Benefits

medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time, paid sick, and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually – These all are subject to applicable eligibility

Seniority Level

Mid-Senior level

Employment Type

Contract

Job Function

Engineering and Science

Industries

Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing

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