Share this Job

Manager I, Peripheral Interventions, Reg Affairs Job

Apply now »
Apply now

Apply for Job

Date: Feb 14, 2019

Location: Maple Grove, MN, US, 55311

Company: Boston Scientific

Additional Locations: (n/a)

 

 

Purpose and Passion • Comprehensive Benefits • Life-Work Integration • Community • Career Growth

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.

 

As the global market leader in peripheral interventions, we offer the broadest portfolio of solutions for treating peripheral artery disease (PAD) and deep vein thrombosis (DVT). We are also focused on our Interventional Oncology portfolio, enabling physicians to minimally invasively treat tumors by delivering targeted and localized embolic and ablative technologies. We’re dedicated to developing technologies that improve outcomes, cut costs and—most importantly—help physicians to save the lives and limbs of more people in more places around the world.

 

Purpose:

In this role, you will be responsible for product lines, technology, managerial, leadership, and employee development activities.

 

Your responsibilities will include:

 

  • Directs and coordinates activities of Regulatory Affairs employees.
  • Provide development opportunities for employees
  • Responsible for diverse product lines including embolization microspheres, microcatheters, guidewires, ablation devices, embolization coils, etc
  • Manage the transition of MDR compliance for Interventional Oncology medical devices
  • Assists in establishing project priorities, allocating resources and workload.
  • Provides technical guidance to team during the course of submission preparation and interaction with regulatory bodies.
  • Reviews and edits submissions prepared by team members.
  • Represents Regulatory Affairs at management updates.
  • Develops and overseas innovative regulatory strategies for new and modified products.
  • Assists with developing and implementing departmental policy and procedure.
  • Provides Regulatory Affairs training/mentoring to employees.
  • Assists with 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.
  • Oversees preparation and submission of global regulatory applications as appropriate as well as internal regulatory file documentation.
  • Oversees review of device labeling and advertising materials for compliance with submissions and applicable regulations; analyzes and recommends appropriate changes.
  • Reviews and signs-off product and manufacturing changes for compliance with applicable regulations.
  • Establish and support a work environment of continuous improvement that supports BSC’s Quality Policy, Quality System and the appropriate regulations for the area they support.  Ensure employees are trained to do their work and their training is documented.

 

 What we’re looking for in you:

 

  • Bachelor’s degree preferably in a scientific, technical discipline or project management, Professional certification(s) preferred
  • 8+ years Regulatory Affairs, Medical Device experience required. US, EU, and International regulatory experience preferred
  • Management experience preferred
  • Demonstrated success in management of regulatory submissions activities including FDA and Notified Body experience
  • Demonstrated success as RA lead on large cross-functional development teams
  • Excellent worldwide regulatory strategic planning skills
  • Submission experience for drug/device combination products preferred (FDA, PMDA, CFDA, ANVISA, Health Canada, TGA, etc.)
  • Experience supporting manufacturing/operations/acquisition driven projects and achieving change approvals globally per business expectations
  • Strong understanding of product development process and ability to effectively partner cross-functionally to develop and influence sound product strategies
  • Strong technical knowledge of medical products
  • Strong technical understanding of relevant procedures, practices, and associated medical terminology
  • Thorough knowledge of product development process and design control
  • Excellent research and analytical skills
  • Excellent people development skills
  • Ability to manage multiple employees and projects simultaneously
  • Excellent written and oral communication, technical writing and editing skills
  • Strong leadership, interpersonal and influencing skills
  • Ability to collaborate and build rapport with cross-functional partners, teams, and external regulatory agencies

 

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

 

Requisition ID: 442247

 


Nearest Major Market: Minneapolis

Job Segment: Medical, Oncology, Manager, Law, Medical Technology, Healthcare, Management, Legal