Abbott Regulatory Affairs Project Manager, Ad/Promo in Abbott Park, Illinois

At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 94,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. Please note that candidates need to be eligible to work in the U.S. without Abbott sponsorship.

JOB DESCRIPTION:

Job Summary:

Review and approve advertising and promotional items to ensure regulatory compliance. Sources may include Digital and social media promotional materials, Sales and marketing training, customer interfacing materials. Ensure external communications meet regulations.

Note: Responsibilities for this position don't include product submissions tied to registration of the product with the authorities.

Position Summary

As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. The individual has department/group/site level influence and is generally recognized as an expert resource within the department. The individual may share knowledge and expertise with others in support of team activities. The individual may identify data needed, obtain these data and ensure that they are effectively presented for the registration of products worldwide.

Main Responsibilities

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Core job responsibilities for this function may include: • Develop new regulatory policies, processes and SOPs and train key personnel on them.

Evaluate regulatory risks of division policies, processes, procedures.

Provide regulatory input to product lifecycle planning.

Monitor regulatory outcomes of initial product concepts and provide input to senior regulatory management.

Assist in the development of multi country regulatory strategy and update strategy based upon regulatory changes.

Assist in regulatory due diligence for potential and new acquisitions.

Utilize technical regulatory skills to propose strategies on complex issues.

Determine submission and approval requirements.

Identify emerging issues.

Monitor trade association positions for impact on company products.

Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions with other members of regulatory and related teams.

Recruit, develop and mentor regulatory professionals.

Assess the acceptability of quality, preclinical and clinical documentation for submission filing.

Evaluate risk of and regulatory solutions to product and clinical safety issues during clinical phases and recommend solutions.

Compile, prepare, review and submit regulatory submission to authorities.

Monitor impact of changing regulations on submission strategies and update internal stakeholders.

Monitor applications under regulatory review.

Communicate application progress to internal stakeholders.

Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities.

Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies.

Negotiate and interact with regulatory authorities during the development and review process to ensure submission approval.

Provide strategic input and technical guidance on regulatory requirements to development teams.

Manage and execute preapproval compliance activities.

Oversee processes involved with maintaining annual licenses, registrations, listings and patent information.

Ensure compliance with product post marketing approval requirements.

Review and approve advertising and promotional items to ensure regulatory compliance.

Ensure external communications meet regulations.

Develop, implement and manage appropriate SOPs and systems to track and manage product-associated events • Actively contribute to the development and functioning of the crisis/issue management program.

Oversee system to ensure that product safety issues and product-associated events are reported to regulatory agencies • Report adverse events to regulatory agencies and internal stakeholders.

Provide regulatory input for product recalls and recall communications.

Accountability

Individuals execute and manage technical and scientific regulatory activities.

Must function independently as a decision-maker on regulatory issues, and must assure that deadlines are met.

Effectively communicate, prepare, and negotiate both internally and externally with various regulatory agencies.

Properly interpret and apply regulatory requirements.

Work is performed without appreciable direction and exercises some latitude in determining technical objectives of assignments.

Completed work is reviewed from a relatively long- term perspective for desired results.

Individual is recognized as a discipline expert and resource in regulatory affairs.

Qualifications

Bachelor's degree (or equivalent), Bachelor’s degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred. M.S. in a technical area or M.B.A. is preferred. A Ph.D. in a technical area or law is helpful. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. 4-5 years’ experience in a regulated industry (e.g., medical products, nutritionals).

Preferred Qualifications

2+ years in Ad/Promo regulatory experience

JOB FAMILY:

Project Management

DIVISION:

ADD Diagnostics

LOCATION:

United States > Abbott Park : AP08/A Floor-1

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

Abbott is about the power of health. For more than 125 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 150 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.

The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of life’s greatest health challenges.

We invite you to explore opportunities at Abbott , to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

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