Job Description

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 109,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

ABOUT ABBOTT DIAGNOSTICS:

The key to successful treatment and full recovery is often fast, accurate diagnosis. Abbotts life-changing tests and diagnostic tools provide insights that enable smarter, faster decisions and transform the way the world is managing health.

Our pioneering technology spans the world of healthcare operations with medical diagnostic instruments, tests, automation and informatics solutions for hospitals, reference labs, blood centers, emergency departments, physician offices and clinics.

Our location in Lake County, Illinois currently has an opportunity for a Regulatory Affairs Specialist - New Product Development

WHAT YOULL DO

As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual may execute tasks and exercise influence generally at the middle management level. The individual may assist in the registration of products by preparing and submitting documentation needed for registration worldwide.

* Provide regulatory input to product lifecycle planning. Assist in SOP development and review.
* Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes.
* Understand and investigate regulatory history/background of class, disease/ therapeutic/diagnostic context in order to assess regulatory implications for approval.
* Determine trade issues to anticipate regulatory obstacles. Participate in risk benefit analysis for regulatory compliance.
* Determine and communicate submission and approval requirements. Monitor applications under regulatory review.
* Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies.
* Assist in preparation and review of regulatory submission to authorities.
* Maintain annual licenses, registrations, listings and patent information.
* Assist compliance with product post marketing approval requirements. Assist in the review of advertising and promotional
* items.
* Assess external communications relative to regulations. Review regulatory aspects of contracts.
* Assist with label development and review for compliance before release.
* Submit and review change controls to determine the level of change and consequent submission requirements.
* Contribute to the development and functioning of the crisis/ issue management program. Ensure product safety issues and product associated events are reported to regulatory agencies.
* Provide regulatory input for product recalls and recall communications.
* Individual may provide limited work direction and guidance to peers and/or skilled non-exempt levels of employees.
* Participates in the development of less experienced staff by setting an example, providing guidance, and offering counsel.
* Plans and organizes non-routine tasks w/approval. Initiates or maintains work schedule. Establishes priorities of work assignments. May lead a departmental project team.
* Establishes and cultivates an extensive network of support to facilitate completion of assignments.
* Participates in determining goals and objectives for projects.
* Influences middle management on technical or business solutions.
* May interact with vendors.
* Exercises judgment in selecting innovative, practical methods to achieve problem resolution. Failure to obtain results or erroneous decisions or recommendations would typically result in serious delays and considerable expenditure of resources.

EDUCATION AND EXPERIENCE YOULL BRING

Required Cant Modify

* Bachelors degree (or equivalent); Bachelors degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred.
* Certification is a plus (such as RACfrom the Regulatory Affairs Professionals Society.)
* This position does not require previous regulatory experience. 2-3 years experience in a regulated industry (e.g., medical products, nutritionals). Regulatory area is preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. Note: Higher education may compensate for years of experience.
* Experience with Regulatory history, guidelines, policies, standards, practices, requirements and precedents Regulatory agency structure, processes and key personnel Principles and requirements of applicable product laws Submission/registration types and requirements GxPs (GCPs, GLPs, GMPs) Principles and requirements of promotion, advertising and labeling Domestic and international regulatory guidelines, policies and regulations Ethical guidelines of the regulatory profession, clinical research and regulatory process Note: This knowledge may be developed through tenure in this position.
* Communicate effectively verbally and in writing Communicate with diverse audiences and personnel Write and edit technical documents
* Work with cross functional teams Work with people from various disciplines and cultures
* Write and edit technical documents.
* Negotiate internally
* Pay strong attention to detail
* Manage projects Create project plans and timelines
* Think analytically and critically.
* Organize and track complex information
* Exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Preferred

* M.S. or Ph.D. in a technical area preferred but not required .
* Experience writing, packaging, and submitting U.S. FDA submissions

WHAT WE OFFER

At Abbott, you can have a good job that can grow into a great career. We offer:

* Training and career development, with onboarding programs for new employees and tuition assistance
* Financial security through competitive compensation, incentives and retirement plans
* Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
* Paid time off
* 401(k) retirement savings with a generous company match
* The stability of a company with a record of strong financial performance and history of being actively involved in local communities

Learn more about our benefits that add real value to your life to help you live fully: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. 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 and @AbbottGlobal.

JOB FAMILY:

Regulatory Operations

DIVISION:

ADD Diagnostics

LOCATION:

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

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 5 % of the Time

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