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Sr. Regulatory Affairs Manager

Abbott

Sr. Regulatory Affairs Manager

full-timePosted: Jan 12, 2026

Job Description

Working at Abbott

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.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU 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 Opportunity

The Sr. Regulatory Affairs Manager hired in this role will work out of the Lake Forest, IL (or ourTown Center, San Diego, CA) 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. 

In addition, the person hired will:

  • 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.

  • Interacts with regulatory agency to expedite approval of pending registration.

  • Serves as regulatory liaison throughout product lifecycle.

  • Participates in some of the following: product plan development and implementation, regulatory strategy, risk management.

  • Serves 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

  • Must have well developed written, oral, interpersonal and negotiation skills.

  • Leadership competency including organizational development and project management skills.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.



The base pay for this position is $113,300.00 – $226,700.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Global

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • regulatory affairs project managementintermediate
  • 510(k) submissionsintermediate
  • CLIA Waiver processesintermediate
  • label/advertising/promotional reviewintermediate
  • risk managementintermediate

Responsibilities

  • Develop and implement regulatory strategies
  • Coordinate regulatory submissions
  • Interface with regulatory agencies
  • Serve as regulatory liaison throughout product lifecycle
  • Participate in product plan development
  • Act as regulatory representative to teams and agencies

Benefits

  • general: free medical coverage (HIP PPO)
  • general: excellent retirement savings plan
  • general: tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit
  • general: great place to work recognition

Target Your Resume for "Sr. Regulatory Affairs Manager" , Abbott

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Abbott logo

Sr. Regulatory Affairs Manager

Abbott

Sr. Regulatory Affairs Manager

full-timePosted: Jan 12, 2026

Job Description

Working at Abbott

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.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with a high employer contribution

  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU 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 Opportunity

The Sr. Regulatory Affairs Manager hired in this role will work out of the Lake Forest, IL (or ourTown Center, San Diego, CA) 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. 

In addition, the person hired will:

  • 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.

  • Interacts with regulatory agency to expedite approval of pending registration.

  • Serves as regulatory liaison throughout product lifecycle.

  • Participates in some of the following: product plan development and implementation, regulatory strategy, risk management.

  • Serves 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

  • Must have well developed written, oral, interpersonal and negotiation skills.

  • Leadership competency including organizational development and project management skills.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.



The base pay for this position is $113,300.00 – $226,700.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Global

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • regulatory affairs project managementintermediate
  • 510(k) submissionsintermediate
  • CLIA Waiver processesintermediate
  • label/advertising/promotional reviewintermediate
  • risk managementintermediate

Responsibilities

  • Develop and implement regulatory strategies
  • Coordinate regulatory submissions
  • Interface with regulatory agencies
  • Serve as regulatory liaison throughout product lifecycle
  • Participate in product plan development
  • Act as regulatory representative to teams and agencies

Benefits

  • general: free medical coverage (HIP PPO)
  • general: excellent retirement savings plan
  • general: tuition reimbursement
  • general: Freedom 2 Save student debt program
  • general: FreeU education benefit
  • general: great place to work recognition

Target Your Resume for "Sr. Regulatory Affairs Manager" , Abbott

Get personalized recommendations to optimize your resume specifically for Sr. Regulatory Affairs Manager. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr. Regulatory Affairs Manager" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for Sr. Regulatory Affairs Manager @ Abbott.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.