Medical Device Engineer Indianapolis - IN - Indiana

Role Descriptions: Roles & ResponsibilitiesSupport Design History File (DHF) activities for medical device development projects.Review update and maintain Global dFMEA documentation ensuring risks are adequately identified analyzed and mitigated.Review update and maintain Global uFMEA documentation based on product use scenarios and user-related risks.Develop and update Preliminary Hazard Analysis (PHA) documentation in accordance with risk management procedures.Support creation and maintenance of product risk management files throughout the development lifecycle.Prepare review and update Product Characterization documents to define product performance and design intent.Create and maintain Product Specification Documents (PSD) ensuring alignment with design requirements and customer needs.Develop and update Critical-to-Quality (CTQ) documents and establish measurable quality requirements.Support development and maintenance of Design Input Design Output Verification and Validation documentation.Ensure traceability between user needs design inputs risk controls verification activities and design outputs.Collaborate with Design Quality Regulatory Manufacturing and Project Management teams to support product development deliverables.Participate in design reviews and provide technical input on risk management and DHF compliance.Support engineering change assessments and associated documentation updates.Review engineering documents for completeness accuracy and compliance with quality system requirements.Identify gaps in documentation and recommend corrective actions.Support audits inspections and compliance activities related to design control and risk management documentation.Contribute to continuous improvement initiatives for product development and design control processes.Ensure all deliverables comply with applicable regulatory quality and Zimmer Biomet procedures and standards.Ability to establish document traceability between User Needs Design Inputs Design Outputs Risk Management Verification and Validation records within Cockpit Cognition.Experience supporting DHF gap assessments document linking metadata management and compliance reviews.Familiarity with digital DHF structure document hierarchy and traceability matrix development.Knowledge of DHF remediation projects and legacy design documentation migration into Cockpit Cognition. Communicate (written and verbal) direction and project plans with appropriate personnel from other departments.

Essential Skills: Roles & ResponsibilitiesSupport Design History File (DHF) activities for medical device development projects.Review update and maintain Global dFMEA documentation ensuring risks are adequately identified analyzed and mitigated.Review update and maintain Global uFMEA documentation based on product use scenarios and user-related risks.Develop and update Preliminary Hazard Analysis (PHA) documentation in accordance with risk management procedures.Support creation and maintenance of product risk management files throughout the development lifecycle.Prepare review and update Product Characterization documents to define product performance and design intent.Create and maintain Product Specification Documents (PSD) ensuring alignment with design requirements and customer needs.Develop and update Critical-to-Quality (CTQ) documents and establish measurable quality requirements.Support development and maintenance of Design Input Design Output Verification and Validation documentation.Ensure traceability between user needs design inputs risk controls verification activities and design outputs.Collaborate with Design Quality Regulatory Manufacturing and Project Management teams to support product development deliverables.Participate in design reviews and provide technical input on risk management and DHF compliance.Support engineering change assessments and associated documentation updates.Review engineering documents for c

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