Specialist II, Peripheral Interventions

Boston Scientific

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life’s work.


At Boston Scientific, our products and technologies are used to diagnose or treat a wide range of medical conditions. We continue to innovate in key areas and are extending our innovations into new geographies and high-growth adjacency markets. In Peripheral Interventions (PI), we develop and market devices to less-invasively treat vascular system blockages in areas such as the carotid and renal arteries and the lower extremities and cancer. Medical Conditions we provide solutions for include: Peripheral Artery Disease (PAD), Deep Vein Thrombosis (DVT), Critical Limb Ischemia (CLI), and Liver Cancer. The solutions for these conditions include all classifications of devices: Peripheral Balloons and Stents, Drug-Eluting Technologies, Thrombectomy Systems, Atherectomy Devices, Wires, Drainage and Coils and Spherical Embolics. We have a robust product line and pipeline, and we will continue to make an investment in Peripheral Interventional treatments.


Purpose Statement:

Responsible for Regulatory Affairs support of post market products and projects including regulatory strategy, submissions, change assessment and compliance. 


Key Responsibilities:

  • Acts as a core team member on sustaining teams, providing regulatory feedback and guidance throughout the product development cycle.
  • Responsible for preparation and submission of regulatory applications, as well as internal regulatory file documentation.
  • Implements regulatory strategies for new and modified medical devices.
  • Reviews and signs-off on product and manufacturing changes for compliance with applicable regulations.
  • Begins to act as a company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding clarification and follow-up of submissions under review.
  • Assists with departmental policy and procedure implementation.
  • Assists with Regulatory Affairs training to cross functional groups.
  • Reviews device labeling and advertising materials for compliance with global submissions and applicable regulations; analyzes and recommends appropriate changes. 


  • 2+ years related experience, medical industry experience preferred
  • Understanding of FDA, European and international regulations
  • Knowledge of medical devices, procedures and terminology
  • Working knowledge of product development process and design control
  • Basic submission and presentation related computer skills, including experience with software applications such as Microsoft Word, Excel, PowerPoint and Adobe Acrobat
  • Ability to manage multiple projects
  • Excellent written and oral communication, technical writing and editing skills.  Ability to translate technical information into a clearly written message for the regulators
  • Quick learner, self-motivated, independent worker
  • Strong technical, research and problem solving skills
  • Team player with excellent interpersonal skills


About us

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.


Boston Scientific is an Equal Opportunity Employer – Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran


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