Design Assurance Engineer III - Urology

Additional Location(s): US-MA-Marlborough; US-CA-Valencia; US-MN-Maple Grove; US-MN-Minnetonka Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance 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 the role: This Design Assurance Engineer III position will work on the Valencia Technologies Integration project, specifically supporting product Design Control integration. This position ensures that during the integration of products and Design Control quality system processes, the product and processes remain safe, of high quality, and compliant with BSC and regulatory requirements. Work mode: At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Marlborough, MA, Valencia, CA or Minnetonka, MN and requires being on-site at least three days per week. Relocation assistance: Relocation assistance is available for this position at this time. Visa sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your responsibilities will include: * Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. * Acts as an effective team member in supporting quality disciplines, decisions, and practices * Work within a cross-functional team to identify and implement effective controls and support integration of design control related products, records, and processes * Write various technical documentation for procedure execution, technical rationale, and evidence of the development process. * Support Design Assurance activities as related to Risk Management remediation, Design Control Quality System integration, and other DA related integration priorities * Support Post Market activities, as necessary, of risk based on post-market signals * Actively participate in the Design Change process to ensure the proposed changes to the products are systemically and thoroughly analyzed and assessed * Demonstrate good working knowledge and application of validation and statistical techniques in compliance with associated regulatory requirements and internal standards. * Support the verification, validation, and usability testing to meet or exceed internal and external requirements * Develop, update, and maintain Design History File and Design Input / Output documentation (Product Specification, Component Specifications, and Prints) * Generate, update, and maintain product risk management tools (e.g., Hazard Analysis, Fault Tree, FMEAs) * Partner with R&D to determine and implement Design Controls based on Risk Management, Customer Needs, and Manufacturing Input. * Partner cross-functionally to identify and support value improvement efforts to support business goals What we’re looking for in you: Required qualifications: * Minimum of a bachelor’s degree in mechanical, electrical, or biomedical engineering (or other related technical discipline) * 3+ years of experience in design assurance, new product development or related medical device / regulated industry experience * Self-motivated with a passion for solving problems and a bias for action * Strong communication skills (verbal & written) * Demonstrated use of Quality tools/methodologies * Ability to effectively work and collaborate in a mixed onsite + remote environment * Demonstrated experience creating detailed technical documents Preferred qualifications: * Experience working with medical electrical equipment and/or active implantables * Quality Integration experience * ISO...