Our start-up medical device client is adding a Design Assurance Manager to the team. The DA Manager works cross-functionally and is responsible for providing Design Assurance representation on teams, facilitating design verification and validation for transfer to manufacturing, and implementing process / product improvements. The manager also supports quality management system process development and execution for applicable processes. The role has shared responsibility for product safety and quality in all stages of product and process development, and ensuring compliance with design specifications, quality management system procedures associated with design assurance, and all applicable regulatory requirements.
Your role with the company :
Responsible for implementing measurement systems analysis and standardizing documented quality tools such as root cause analysis, flowcharts, cause and effect diagrams, control charts, APQP / PPAP, FMEA, DOE, and other applicable statistical methods.
- Responsible for developing, improving, and managing design assurance processes such as failure analysis, design verification and validation, risk management, design and process-related CAPAs, and complaint handling processes.
- Manage the risk management process by ISO 14971, including risk management plans, hazard analysis, user risk analysis, FMEAs, and risk management reports, throughout all product development phases.
- Responsible for tracking, analyzing, and reporting on quality and business measurements such as design verification failures, complaints, and CAPAs. Supports the analysis and evaluation of design verification capabilities and the design and development of new products from the design assurance perspective.
- Partner with other functional areas, primarily R&D, in areas such as preparing test plans, data analysis, specifications, risk analysis, proposed change assessments, and change implementation. Interpret and contribute to electro-mechanical systems, software design, and testing. Ensure clarity and consistency in acceptance criteria and ensure the verification processes used are capable and statistically relevant.
Manage People
Manage DA staff and technical improvement projectsTechnically excellent with deep and broad experience in DAHands-on, dives in, takes ownershipData visibility and integration into our DA processesUse of Quality Tools - routine use of documented root cause analysis and other Quality ToolsManage Products
Responsible for all Design Assurance activities for Francis Medical capital, reusable, disposable, and software productsExperience with biocompatibility, human factors, electrical safety, hardware, and sterilization industry standards and testing.Manage Processes
Data Analysis : standardized use of statistical tools across QMSRoot Cause Analysis : standardized documented use of Quality ToolsDA processData visibility and integration into our processes, broad implementation of JMPEfficient and effective verification processes that measure and report all aspects of the verification processPlanning - test method metrics (who, how long, sequencing efficiency)Execution - coordination and real-time visibility to statusFailure Analysis for complaints, NCM, CAPA - key process for DAReporting - JMP ready, real-time reporting, stability / capabilityRisk Management processIEC 60601 compliant risk management fileJAMA Direct implementationGAS risk management module implementationUsability of risk management system by engineers and regulatory, visibility for QMS reviewCorrective and Preventive Action (CAPA) - design and process related CAPAsComplaint investigation, failure analysis, and reportingDesired Profile :
BS Engineering (EE, ME, BME) ideal
Certifications (ASQ CQE, SSBB, MQ / OE, CSCP, CQA)
Experience managing people and in-depth knowledge of Quality Management System processesMinimum 10 years of experience working in the medical device industry.Breadth across development timelines, across functions, and company sizesDepth into each area of QA, hands on involvement, experience, and learningProficient in statistics and statistical software, preferably JMPCuriosity, learning, strong work ethic, getting involved, continuously improvingOutstanding integrity, character, and trustworthiness; demonstrated evidence of leadership, creativity, adaptability, determination, perseverance and excellent communicationAbility to respond to inquiries or complaints from customers, regulatory agencies, or members of the business community in all areas of Quality Assurance.Experience in statistics, statistical software, and Quality Tools a plus