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Senior Regulatory Affairs Specialist - Structural Heart

Company: Abbott Laboratories
Location: Saint Paul
Posted on: June 10, 2021

Job Description:

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.

Structural Heart Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. We aim to lead the markets we serve by requiring the solutions we offer customers provide an improved benefit/risk profile as compared to existing standards of care; a performance threshold that by definition, guides and ensures the productive output of our engineering, business development, and clinical research efforts result in outcomes that advance the standard of care.

We are recruiting for a Senior Regulatory Affairs Specialist to join our team in the St. Paul, MN or Santa Clara, CA location. In this role, you be responsible for coordinating, planning, preparation, assembly, and review of regulatory submissions to the FDA and other worldwide regulatory agencies.


  • Develops domestic and/or international strategies for regulatory approval of company products
  • Coordinates, compiles and submits U.S, and/ or International regulatory submissions, including filing and/or creation of PMAs, IDEs, Premarket Notifications, Supplements, Change Notifications, and other country-specific product registrations
  • Prepares robust regulatory applications to achieve departmental and organizational objectives
  • Represents RA on cross-functional product development and manufacturing support teams. Guide teams to provide content for US and/or International submissions, participates in design reviews as needed
  • Acts as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detail
  • Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are current, up-to-date and are entered into regulatory submission data base and file systems. Ensures that information of such regulations and requirements, especially those that are new or modified, are distributed to appropriate personnel
  • Reviews device labeling and marketing materials for compliance with FDA submissions and applicable regulations
  • Supports the product release process by creating GTS licenses or reviewing and approving requests for product release
  • Interfaces directly with U.S. Food and Drug Administration (FDA) and other regulatory agencies.
  • Conducts reviews of product and manufacturing changes for compliance with applicable regulations. Reviews protocols and reports to support regulatory submissions. Creates, reviews and approves engineering change orders
  • Communicates with and maintain productive, constructive relationships with external customers as required - US FDA, Health Canada, regulatory representatives, and notified-bodies
  • Support Department and Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
  • Complies with FDA and international regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
  • Provides mentoring and leadership to Regulatory Specialist I and II team members.
  • Performs other related duties and responsibilities, on occasion, as assigned



  • Bachelor's Degree in life sciences or engineering, or other technical discipline
  • 5+ years of technical experience, including at least 4 years of regulatory experience in a medical device industry
  • Class III medical device experience
  • Experience with, IDE supplements, PMA supplements, and US device regulations and/or experience with EU and other international medical device regulations and submissions
  • Must be familiar with relevant US/international regulatory requirements for medical devices including Quality Systems standards and clinical investigations
  • Proficient with MS Office Suite (Word, Excel, PowerPoint, Outlook)
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization


  • Transcatheter valve experience a plus
  • Experience working in a broader enterprise/cross-division business unit model
  • Ability to work in a highly matrixed and geographically diverse business environment


At Abbott, you can have a good job that can grow into a great career. We offer:

  • Training and career development, with onboarding programs for new employees and tuition assistance
  • Financial security through competitive compensation, incentives and retirement plans
  • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
  • Paid time off
  • 401(k) retirement savings with a generous company match
  • The stability of a company with a record of strong financial performance and history of being actively involved in local communities

Learn more about our benefits that add real value to your life to help you live fully:

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at, on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.

Keywords: Abbott Laboratories, St. Paul , Senior Regulatory Affairs Specialist - Structural Heart, Other , Saint Paul, Minnesota

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