Minnesota Staffing
Senior Design Assurance Engineer
Minnesota Staffing, Saint Paul, Minnesota, United States, 55130
Senior Design Assurance Engineer
At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information, and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About This Role:
This Senior Design Assurance Engineer on the Field CAPA team will lead cross-functional teams to determine actionable root cause and implement effective solutions for high visibility issues impacting Active Implantable & Accessories product performance within the Cardiac Rhythm Management and Diagnostics (CRMDx) division. This role is a tremendous opportunity for a strong technical individual, with an innate technical curiosity, who is seeking leadership, complex problem-solving, and project management experience. The role also provides great exposure to the intricacies of how CRMDx products function, are designed, and the many parts of the organization that support their commercial use. This individual will collaborate and partner with Research & Development, Regulatory, Marketing, Medical Safety, Manufacturing, Post Market, and other Quality organizations to achieve optimal results. May serve as liaison between the company and the various governmental agencies worldwide. Your Responsibilities Will Include:
Leads cross-functional teams on complex product performance investigations, where suspected root cause is product design. Includes Nonconforming Events and Preventions (NCEPs), Product Inquiry Reports (PIRs), and Corrective and Preventive Actions (CAPAs). Expected to facilitate high performing teams working towards common goals and timelines. Leads collaborative problem solving of complex technical issues using disciplined, methodical techniques. Tools used include DMAIC, Root Cause Analysis, 5 Whys, Cause & Effect Diagram, and Is-Is Not. Creates, maintains, and enhances cross-functional team partnerships. Provides guidance regarding technical strategies and approaches; works cross-functionally and across multiple sites in identifying and resolving technical issues. Represents the team at key global and divisional leadership forums. Creates and maintains detailed investigation documentation following Good Documentation Practice guidelines. Creates, reviews, and approves Quality System records for NCEPs, PIRs, and CAPAs. May represent NCEPs, PIRs, and CAPAs in internal and external audits. Presents updates in formal and informal reviews with all levels of the organization including high senior leadership at Boston Scientific. Mentors and guides other cross-functional teams and engineers by providing technical guidance and consulting on execution of NCEPs, CAPAs, and PIRs. May include consulting across other BSC divisions. Participates on behalf of the Field CAPA or Design Assurance team at large in Global Communities of Practice to foster cross-communication, best practices, and improvement to investigational processes and outcomes. Focuses on continuous improvement by championing and fostering the execution of projects within the local and divisional Design Assurance organizations. Fosters a diverse and inclusive workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. Monitors and ensures compliance with company policies and procedures. Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. What We're Looking For In You:
Required Qualifications Bachelors degree in an engineering or related discipline with 5+ years of relevant experience or Masters with 3+ years of relevant experience. Experience in Medical Device industry knowledgeable in Quality System Regulations, Medical Device Regulation, and ISO 13485 Quality Standards. Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook. Experience with NCEPs, CAPAs, PIRs and/or other investigation processes. Ability to collaborate and influence across multiple, cross-functional teams Demonstrated technical problem-solving & data analysis capabilities Preferred Qualifications Experience with Class III Active Implantable technologies and the CRMDx division Experience with statistics and statistical analysis tools (e.g. MINITAB, Weibull++) Strong ability to successfully multi-task and demonstrate adaptability Project management experience (direct or cross-functional teams) Demonstrated effective change leadership and results-oriented focus Strong business acumen and communication skills, with the ability to quickly establish impact and consequences Demonstrated experience managing and leading multiple projects covering diverse engineering (i.e. Software, Hardware, Labeling) disciplines and functions. Self-starter with the ability to identify improvement opportunities. Comfort speaking to groups of individuals including divisional senior leaders. Presentation skills that comfortably and concisely translate performance and issues to peer and senior management audiences.
At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information, and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About This Role:
This Senior Design Assurance Engineer on the Field CAPA team will lead cross-functional teams to determine actionable root cause and implement effective solutions for high visibility issues impacting Active Implantable & Accessories product performance within the Cardiac Rhythm Management and Diagnostics (CRMDx) division. This role is a tremendous opportunity for a strong technical individual, with an innate technical curiosity, who is seeking leadership, complex problem-solving, and project management experience. The role also provides great exposure to the intricacies of how CRMDx products function, are designed, and the many parts of the organization that support their commercial use. This individual will collaborate and partner with Research & Development, Regulatory, Marketing, Medical Safety, Manufacturing, Post Market, and other Quality organizations to achieve optimal results. May serve as liaison between the company and the various governmental agencies worldwide. Your Responsibilities Will Include:
Leads cross-functional teams on complex product performance investigations, where suspected root cause is product design. Includes Nonconforming Events and Preventions (NCEPs), Product Inquiry Reports (PIRs), and Corrective and Preventive Actions (CAPAs). Expected to facilitate high performing teams working towards common goals and timelines. Leads collaborative problem solving of complex technical issues using disciplined, methodical techniques. Tools used include DMAIC, Root Cause Analysis, 5 Whys, Cause & Effect Diagram, and Is-Is Not. Creates, maintains, and enhances cross-functional team partnerships. Provides guidance regarding technical strategies and approaches; works cross-functionally and across multiple sites in identifying and resolving technical issues. Represents the team at key global and divisional leadership forums. Creates and maintains detailed investigation documentation following Good Documentation Practice guidelines. Creates, reviews, and approves Quality System records for NCEPs, PIRs, and CAPAs. May represent NCEPs, PIRs, and CAPAs in internal and external audits. Presents updates in formal and informal reviews with all levels of the organization including high senior leadership at Boston Scientific. Mentors and guides other cross-functional teams and engineers by providing technical guidance and consulting on execution of NCEPs, CAPAs, and PIRs. May include consulting across other BSC divisions. Participates on behalf of the Field CAPA or Design Assurance team at large in Global Communities of Practice to foster cross-communication, best practices, and improvement to investigational processes and outcomes. Focuses on continuous improvement by championing and fostering the execution of projects within the local and divisional Design Assurance organizations. Fosters a diverse and inclusive workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. Monitors and ensures compliance with company policies and procedures. Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. What We're Looking For In You:
Required Qualifications Bachelors degree in an engineering or related discipline with 5+ years of relevant experience or Masters with 3+ years of relevant experience. Experience in Medical Device industry knowledgeable in Quality System Regulations, Medical Device Regulation, and ISO 13485 Quality Standards. Proficient with Microsoft Office tools including Word, Excel, PowerPoint, and Outlook. Experience with NCEPs, CAPAs, PIRs and/or other investigation processes. Ability to collaborate and influence across multiple, cross-functional teams Demonstrated technical problem-solving & data analysis capabilities Preferred Qualifications Experience with Class III Active Implantable technologies and the CRMDx division Experience with statistics and statistical analysis tools (e.g. MINITAB, Weibull++) Strong ability to successfully multi-task and demonstrate adaptability Project management experience (direct or cross-functional teams) Demonstrated effective change leadership and results-oriented focus Strong business acumen and communication skills, with the ability to quickly establish impact and consequences Demonstrated experience managing and leading multiple projects covering diverse engineering (i.e. Software, Hardware, Labeling) disciplines and functions. Self-starter with the ability to identify improvement opportunities. Comfort speaking to groups of individuals including divisional senior leaders. Presentation skills that comfortably and concisely translate performance and issues to peer and senior management audiences.