Boston Scientific Senior Design Assurance Engineer 

United States, Minnesota 

92277384

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.

Maximum Salary: $ 156900

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.