Boston Scientific Senior Regulatory Affairs Specialist 

United States, Minnesota, Arden Hills 

787224389

US-MN-Arden Hills

At Boston Scientific, you’ll discover a place where you can have meaningful purpose, improving lives through your life's work. In Rhythm Management (RM) we offer solutions for treating irregular heart rhythms and heart failure and protecting against sudden cardiac arrest. We continue to innovate in key areas and extending our products into new geographies and high-growth adjacency markets.
About this role:
The Senior Regulatory Specialist is responsible for activities which lead to and maintain regulatory approval to market devices. Additionally, the Specialist is responsible for assessment of device changes for regulatory implications.

This is a hybrid position (in office minimum three days per week) with the flexibility to be located in Arden Hills, MN or Waltham, MA. You will have the opportunity to discuss your preferred working location with your Talent Acquisition Specialist.

Your responsibilities will include:

• Develop domestic and international strategies for regulatory approval of Class I, II and III medical devices, specifically capital equipment with software

• Coordinate, compile, and submit U.S. and EU regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, PMA & IDE Annual Reports, and CE Mark submissions under MDR

• Support requests from BSC International Regulatory personnel related to submissions, registrations, and change assessments

• Develop and maintain positive relationships with regulatory body reviewers

• Review Technical and Labeling documentation for inclusion in regulatory filings

• Review product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings

• Represent RA on cross functional projects which may include product development, sustaining changes, and continuous improvement efforts

• Review clinical study protocols and other clinical documentation, and assess clinical study related changes to determine regulatory impact

• Support regulatory audits, as required

• In all actions, demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.

Required Qualifications:

• A minimum of a Bachelor's Degree

• A minimum of 5 years of regulatory affairs or related experience

• Demonstrated experience authoring/supporting a variety of regulatory submissions for US and EU, such as original PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s and MDR Tech Docs.

• Experience working with capital equipment and/or software medical devices

• Basic submission and presentation related computer skills, including experience with the software applications Microsoft Word, Excel, PowerPoint and Adobe Acrobat

Preferred Qualifications:

• Strong technical, research and problem-solving skills

• Ability to articulate complex ideas clearly both verbally and in writing

• Team player with excellent interpersonal skills

• Demonstrated ability to effectively manage multiple projects and priorities

• Works well in fast-paced cross-functional team environments

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.