Principal Regulatory Affairs Specialist
AbbottAbout the role
JOB DESCRIPTION:
Principal Regulatory Affairs Specialist
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
This position is based at the Abbott Park, IL (Lake Bluff, IL) or Willis Tower, IL (Chicago, IL) location within the Transfusion Medicine business. Our diagnostic solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers.
As the Principal Regulatory Affairs Specialist, you’ll be an individual contributor, combing knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured, or distributed to meet required legislation. The individual has department level influence and is generally recognized as an expert resource within the department. The individual shares knowledge and expertise with others in support of team activities. The individual helps identify, obtain, and effectively present data for the registration of products worldwide.– CAN Modify
What You’ll Work On
Knowledge base includes: domestic and international regulatory policies/requirements, submissions/registration types, and advertising and labeling promotional requirements
Interprets and implements regulatory requirements
Defines regulatory strategies and performs regulatory assessments
Exercises sound and ethical judgment
Compiles, prepares, reviews, and submits regulatory submissions to authorities
Negotiates internally and externally with regulatory agencies
Effectively communicates verbally and in writing with diverse audiences and personnel
Writes and edits technical documents
Clear articulates plans/strategies regarding significant matters with managers and directors, often requiring the coordination of activities across business units
Participates in the development of others by facilitating training and providing feedback and guidance
Creates and executes project plans and timelines
Organizes and tracks complex information
Thinks both analytically and critically
Works with cross-functional teams from various disciplines and cultures
May lead a cross-functional project team
Has broad knowledge of various technical alternatives and their potential impact on the business
Provides technical leadership to business units
Follows scientific arguments, identifies regulatory scientific data needs, and solves regulatory issues
Uses in-depth knowledge of business units and cross group dependencies/ relationships
Required Qualifications
Bachelors Degree in Scientific discipline e.g. Chemistry, life Sciences, Biology (or equivalent vocational qualifications).
E
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s