Principal Product Analyst

Boston Scientific•Arden Hills, MN

13h•Hybrid

About The Position

Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. Everyone at Boston Scientific works toward one goal: transforming lives by addressing the most critical challenges in the medical device industry. Patient care is at the heart of everything we do, and ensuring quality, compliance and positive outcomes is essential to delivering on that commitment. As a principal product analyst, you will lead strategic initiatives that enhance product quality and performance across global markets. You will collaborate with a high-performing, cross-functional team to solve complex challenges, applying data-driven insights to identify risks, improve processes and drive decisions that make a lasting impact on health care worldwide. This role offers the opportunity to contribute to meaningful change as part of a team that thrives on shared success.

Requirements

Bachelor’s degree, preferably in a scientific, engineering or technical discipline
Minimum of 5 years' experience in the medical device, pharmaceutical or diagnostic device industry
Demonstrated ability to adapt to and contribute to changing priorities
Proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint and Visio
Working knowledge and practical application of FDA, ISO and MDR regulations within the medical device industry
Demonstrated proficiency in project management

Nice To Haves

Experience with post-market activities, including complaints and vigilance
Experience with corrective and preventive action (CAPA) processes
Strong research, communication and presentation skills
Strong written and verbal communication, including technical writing and editing
Ability to work independently with minimal direction or supervision
Experience with SAS, Snowflake or similar analytics and querying tools

Responsibilities

Ensure compliance with U.S. and global regulatory requirements for medical device complaint handling and reporting
Lead and contribute to large, high-impact global quality initiatives to improve post-market quality across divisions
Drive and coordinate cross-functional, multi-site collaboration to deliver on project milestones, timelines and objectives
Communicate clearly and concisely with senior leadership on project progress, risks and key deliverables
Promote and model a positive, solution-oriented team culture through strong communication, resilience and high-quality execution
Identify, escalate and resolve risks, respectfully challenging the status quo while providing recommendations and driving solutions
Apply systems thinking to streamline processes, identify risks and improvement opportunities, and implement improvement plans
Maintain clear communication within the department by keeping teams informed of relevant changes and their operational impact
Utilize data and analytics to identify risks, opportunities and priorities
Support the development and implementation of standard operating procedures and work instructions to improve and standardize complaint regulatory reporting processes
Support internal and external audits
Work independently and effectively across a global organization
Demonstrate a primary commitment to patient safety and product quality by maintaining compliance with the quality policy and all documented quality processes and procedures