Principal Product Analyst

Principal Product Analyst

Work mode: Hybrid Onsite Location(s): Arden Hills, MN, US, 55112 Additional Location(s): N/A 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: 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.

Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. 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:

• 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

Qualifications: Required qualifications: 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 Preferred qualifications: 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