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Job description (Tasks/Responsibilities):
Develops, establishes and maintains quality engineering methodologies, systems, and
practices which meet requirements established by Spectranetics, customers and
regulatory agencies. Serves as a Quality representative to improve awareness,
visibility, and communication on quality initiatives. Provides focused quality
engineering support within new product development. Maintains Risk Management documentation and provides Quality Engineering
support for the life cycle of all Spectranetics products. Provide QA
leadership to project and system for the fill lifecycle of the product, service
or system. Develop, update
and maintain SOPs, forms, methods related to Quality in the NPI/DC SOP and Risk
Management system. Ensure Risk Management is effective utilizing feedback from validation, field safety,
manufacturing indicators, CAPAs, HHAs, ect. Lead and support
Health Hazard Analysis to ensure risk assessment and root cause analysis across
products and systems.
Skill Requirements:
Strong and solid experience in Risk Management for medical devices. Application and
leading problem-solving, root cause analysis and related Corrective and
Preventive Action (including verification). Experience with Health Hazard
Analysis. Familiarity with ISO 14971 Medical devices engineering.
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Company Description:
Spectranetics Corporation engages in the development, manufacture, marketing, and
distribution of single-use medical devices used in minimally invasive surgical
procedures within the cardiovascular system in the United
States, Europe and Japan. Spectranetics Corporation was founded in 1984 and is based in Colorado
Springs, Colorado.
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