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Local to Rochester NY_Medical Device Validation engineer

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: 360 IT Professionals
Full Time position
Listed on 2026-01-07
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: City of Rochester

Local to Rochester NY Medical Device Validation Engineer

360 IT Professionals is seeking a mid-level Medical Devices Validation engineer in Rochester, NY.

We are looking for a candidate with a minimum of a BA/BS in Life Sciences, Engineering, Physical Science or a related discipline; an MA/MS in Life Sciences, Engineering, or Physical Science is preferred.

  • A minimum of a BA/BS in Life Sciences, Engineering, Physical Science or a related discipline is required; an MA/MS in Life Sciences, Engineering, or Physical Science is preferred.
  • Must have at least 5 years of related experience in Medical Device quality system management, including experience in working under Design Control.
  • Effective oral & written communication skills are required.
  • Works independently and sets an example in ensuring compliance to Design Controls and other Quality System requirements to assigned project(s).
  • Utilizes Six Sigma/Process Excellence to solve complex problems and develop optimal product performance.
  • Partners with R&D, Operations, Quality, Regulatory and Compliance, suppliers and other groups to ensure effective product development and transfer of knowledge.
  • Provides technical input as appropriate.
  • Ensures effective implementation of risk management requirements to prevent unanticipated failure modes and quality issues.
  • Provides input as needed to regulatory inspections.
  • Executes Failure Investigations and corrections of design related quality issues.
  • Utilizes advanced Quality Engineering tools (data analysis, statistics, sampling plans, etc.) to ensure effective product development.
  • Participates in post-product launch failure investigations.
  • Provides guidance and leadership to junior members of the team.
  • Suppliers/External Manufacturers:
    Directly or indirectly support design change control activities.
  • Review and approve plans/protocols and reports, deviations/nonconformances, and document changes through the change control processes for accuracy and completeness.
  • Proactively identifies issues, troubleshoots issues, and escalates concerns as appropriate. Adheres to strict procedural and quality standards including thorough and accurate documentation, testing protocols

Webcam Interviews are acceptable for this position.

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