Senior Product Analyst

Additional Location(s) US-MN-Arden Hills; US-CA-Valencia About the role As a Senior Product Analyst, you will be part of a dynamic team dedicated to enhancing product quality and performance across global markets. In this role, you will analyze customer complaints within the Neuromodulation Division's Complaint Management Center (CMC) and collaborate with cross‑functional partners to solve complex challenges. By leveraging data‑driven insights, you will identify risks, improve processes and support critical decisions that have a lasting impact on healthcare worldwide. This position offers the opportunity to drive meaningful change while contributing to a team culture built on collaboration, innovation and shared success. Work model, sponsorship, relocation This position is based on‑site. Employees are expected to work from the assigned Boston Scientific facility on a full‑time basis. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. Your responsibilities will include Serve as a positive influence on team culture by modeling high‑quality work, effective communication, resilience and solution‑oriented thinking. Ensure compliance with U.S. and international regulatory requirements for medical device complaint handling and regulatory reporting. Review complaint communications and assess regulatory compliance, reportability and potential impact to patient safety and business operations. Apply clinical knowledge related to product applications to evaluate identified complaints and conduct investigations by gathering information from clinical staff, field representatives, internal stakeholders and laboratory analyses. Establish regulatory reportability decisions using hazard analyses, Design Failure Mode and Effects Analysis (DFMEA), reported event information, investigation findings and regulatory decision models. Apply appropriate coding to complaint events to support product performance records and collaborate with engineering, laboratory and other internal teams to review coding and investigation outcomes. Compose clear and comprehensive written communications detailing clinical observations, investigations, product analyses and corrective actions, as applicable, for physicians and other end‑user customers. Support and lead divisional initiatives and strategic priorities. Review peer work products and provide constructive feedback while identifying opportunities for process improvement. Utilize data and analytics to identify risks, opportunities and business priorities. Provide clear, concise communications and presentations to leadership regarding deliverables, timelines and milestones. Influence change and align stakeholders to support decision‑making in situations with limited information. Apply systems‑thinking principles to identify process improvement opportunities, mitigate risk and enhance quality system effectiveness. Support training activities and knowledge‑sharing initiatives across the organization. Identify and elevate risks appropriately, respectfully challenge assumptions when necessary and provide recommendations to resolve issues. Work independently and collaboratively across functions to achieve business objectives. Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all documented quality processes and procedures. Required qualifications Bachelor's degree in a scientific, technical or related discipline. Minimum of 5 years' experience in the medical device industry. Demonstrated ability to adapt to changing priorities and contribute effectively in a dynamic environment. Proficiency with Microsoft Office applications, including Word, Excel and PowerPoint. Working knowledge and practical application of FDA, ISO and other applicable medical device regulations. Preferred qualifications Experience supporting corrective and preventive action (CAPA) activities. Experience handling complaints for neuromodulation or implantable medical device products. Strong research, communication and presentation skills. Strong technical writing, editing and documentation skills. Ability to work independently with minimal direction or supervision. Experience utilizing data analytics to support quality, compliance or business decision‑making. Proven ability to influence cross‑functional stakeholders and drive process improvements. Experience presenting recommendations and project updates to leadership audiences. Requisition ID : 630245 Minimum Salary :$71500 Maximum Salary :$135800 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see – will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non‑exempt (hourly), non‑sales roles may 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 for exempt, non‑sales roles may 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 U.S. 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. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. #J-18808-Ljbffr Boston Scientific