Associate Director Regulatory Affairs

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.

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

This position, Associate Director Regulatory Affairs , works out of our San Diego, CA location in the Infectious Diseases Division. This role is part of the RA New Product Introduction (NPI) team, reporting to the Director of Global NPI and U.S. Regulatory Affairs. 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.

We are seeking a highly knowledgeable individual to combine expertise in scientific, regulatory, and business issues to ensure our products meet required legislation. This role involves significant departmental influence and recognition as an expert resource both within Abbott and externally.

Responsibilities include interfacing with regulatory agencies and trade associations and providing executive management with regulatory metrics and information. The individual will ensure data is identified, obtained, and effectively presented for product registration worldwide (US, FDA, CE-IVDR, PMDA, etc.).

Strategic Planning :

Premarket :

Requirements

Regulatory Knowledge of (as applicable) :

Preferred Qualifications

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 $146,700.00 – $293,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY :

Regulatory Operations

DIVISION :

ID Infectious Disease

LOCATION : United States >

San Diego : 4545 Towne Center Court

WORK SHIFT : Standard

TRAVEL :

Yes, 10 % of the Time

MEDICAL SURVEILLANCE :

No

SIGNIFICANT WORK ACTIVITIES :

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)

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