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Sr. Regulatory Affairs Manager

Sr. Regulatory Affairs Manager

Illinois StaffingLake Forest, IL, US
11 hours ago
Job type
  • Full-time
Job description

Sr. Regulatory Affairs Manager

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 114,000 colleagues serve people in more than 160 countries.

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to :

  • Career development with an international company where you can grow the career you dream of.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement, the student debt program, and education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Sr. Regulatory Affairs Manager hired in this role will work out of the Lake Forest, IL location 4-5 days a week in the office. This role will require some travel up to 25% to Abbott locations potentially in and outside of the US. This is part of the Infectious Diseases Division at Abbott Rapid Diagnostics.

This role reports to the leader that also leads Global New Product Introductions and US Regulatory. We're empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott's diagnostics instruments, providing lab results for millions of people.

What you will do :

  • Provide regulatory affairs project management for various areas, to include 510(k), CLIA Waiver, label / advertising / promotional review, and other regulatory compliance activities.
  • In collaboration with the Regulatory leadership, develop and implement regulatory strategies that will ensure earliest possible introduction of product(s) into domestic and international markets.
  • Coordinate preparation of well organized, complete and scientifically sound regulatory submissions.
  • Interface directly with various regulatory agencies, as required, to facilitate the review and approval of regulatory applications.
  • Exercise judgement within generally defined practices and departmental standard operating procedures.
  • Develop and maintain strong and effective relations with internal / external personnel.
  • Interact with regulatory agency to expedite approval of pending registration.
  • Serve as regulatory liaison throughout product lifecycle.
  • Participate in some of the following : product plan development and implementation, regulatory strategy, risk management.
  • Serve as regulatory representative to marketing, research teams and regulatory agencies.
  • Advises development and / or marketing teams on manufacturing changes, technical labeling, appropriate regulations and interpretations.
  • Keep abreast of regulatory requirements in the US and countries where the Division intends to offer product for sale.
  • Work with the Regulatory leadership to prepare regulatory plan / strategy for product introductions.
  • Manage the preparation of registration documents as required for international markets.
  • Ensure that submissions are complete, properly formatted, and comply with applicable regulatory requirements.
  • Make certain that appropriate documentation is maintained to record regulatory decisions made in design and development activities.
  • Minimum Qualifications :

  • Bachelor's Degree Preferably in scientific or engineering related disciplines or an equivalent combination of education and work experience.
  • At least 6 years or more of experience in a similar role in similar organization.
  • Preferred Qualifications :

  • Advanced degree or additional professional training in regulatory affairs (RA) desired.
  • At least 3 years of experience with molecular and lateral flow assays.
  • Well developed written, oral, interpersonal and negotiation skills.
  • Leadership competency including organizational development and project management skills.
  • The base pay for this position is $111,300.00 $222,700.00. In specific locations, the pay range may vary from the range posted.

    Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com.

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    Manager Regulatory • Lake Forest, IL, US

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