Regulatory Affairs Specialist I

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.

We will consider qualified applicants of all ages who are starting (or restarting) their careers 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   About the Role

The Regulatory Affairs Specialist I supports product development, regulatory submissions, global registrations, and regulatory compliance activities throughout the medical device lifecycle. Working under the guidance of experienced regulatory professionals, this role partners with cross-functional teams to assist with regulatory strategy, prepare and maintain submission documentation, assess product and manufacturing changes, support continued market access, and promote quality and continuous improvement.

Your Responsibilities Will Include

Assist in developing and maintaining productive relationships with regulatory agency and notified body reviewers through clear oral and written communications regarding regulatory pathways, testing requirements, submission questions, clarifications, and follow-up activities.

Assist in drafting and implementing regulatory strategies for new and modified medical devices to include Mechanical Circulatory Support systems.

Support cross-functional development teams by providing regulatory feedback and guidance throughout the product development cycle.

Coordinate and compile team inputs and supporting documentation for U.S., EU, and other global regulatory submissions.

Assist with preparation, submission, and maintenance of regulatory applications and internal regulatory file documentation.

Support international regulatory partners in obtaining and maintaining product registrations and approvals.

Review device labeling and advertising materials for consistency with approved submissions and applicable regulatory requirements; analyze and recommend appropriate changes.

Review product, design, manufacturing, supplier, and process changes to assess regulatory impact and support compliance with applicable requirements.

Prepare and maintain change impact assessments and other regulatory records supporting continued compliance with regulatory agency approvals.

Understand and support product lifecycle processes, including sustaining and regulatory approval maintenance activities.

Demonstrate commitment to patient safety, product quality, the Quality Policy, and applicable quality system regulations through daily work practices.

Bachelor's degree in Genetics and Genomics.

Must be eligible to work in the United States without company sponsorship, now or in the future, for employment-based work authorization.

At least three months of experience in Regulatory Affairs.

Prior internship experience with Boston Scientific.

Familiarity with U.S. FDA, EU medical device, and international regulatory requirements.

Experience supporting technical writing, document review, change assessment, or product development activities.

Master's degree in Biotechnology .

Experience or coursework related to medical devices, biotechnology, engineering, quality, clinical research, or regulatory affairs.

Strong written and verbal communication skills, including the ability to analyze, organize, and clearly present technical