Boston Scientific Regulatory Affairs Specialist III 

United States, Massachusetts, Marlborough 

237559635

US-MA-Marlborough; US-MN-Arden Hills; US-MN-Maple Grove; US-MN-Minnetonka

About this role:

At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work.  In the Urology division, we continually advance the quality of patient care with innovative urology solutions. We have a robust product line and pipeline, and we will continue to make an investment in Urology treatments.  This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. The role requires strong US, EU, China, and international regulatory experience that can be leveraged to help support international expansion.

This is a hybrid position (in office minimum three days per week) ideally in Marlborough, MA with the flexibility to be located in Arden Hills, Maple Grove or Minnetonka, MN. You will have the opportunity to discuss your preferred working location with your Talent Acquisition Specialist.
Your responsibilities will include:

• Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams
• Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow-up of submissions under review
• Develops and implements regulatory strategies for new and modified products
• Acts as a core member on manufacturing and development teams, providing regulatory feedback and guidance throughout the product development cycle, and coordinating team inputs for submissions
• Responsible for preparation and submission of global regulatory applications, as well as internal regulatory file documentation
• Reviews device labeling and advertising materials for compliance with global regulations; analyzes and recommends appropriate changes
• Reviews and signs-off on product and manufacturing changes for compliance with applicable regulations
• Support and maintain Quality initiatives in accordance with BSC Quality Policy
• Continuously assess ways to improve Quality
• Develops and implements departmental and divisional policies and procedures
• Supports highly technical or major business segment product lines, special projects or strategic initiatives

Required Qualifications:

• A minimum of a Bachelor’s Degree in a scientific, technical, or related discipline
• A minimum of 3 years Regulatory Affairs experience in the medical industry
• Prior experience with 510(k) submissions, EU MDR or international regulatory registrations

Preferred Qualifications:

• Working knowledge of FDA, EU and international regulations for medical devices
• General understanding of product development process, design control and quality system regulations
• Ability to simultaneously manage several projects
• Proficiency with Microsoft Office
• Effective research and analytical skills
• Effective written and oral communication, technical writing and editing skills
• Ability to work independently with minimal supervision

Please be advised that certain US 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.