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. **_Senior Specialist - Regulatory Affairs -Transfusion_** **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and 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 high employer contribution + Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU (https://www.abbott.com/corpnewsroom/strategy-and-strength/college-degree-for-free-its-possible-with-freeu.html) 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** Our location in Lake Bluff, IL, currently has an opportunity for a **Senior Specialist - Regulatory Affairs** . As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for on-market regulatory affairs department to ensure efficient and compliant business processes and environment. The individual may execute tasks and play a consultative role by partnering across business functions. The individual may assist in identifying data needed, obtaining these data and ensuring that they are effectively presented for the registration of products worldwide. The individual may prepare and submit documentation needed for registration worldwide (domestic and international) or may oversee such preparation. **What You’ll Work On** + Participate as the regulatory functional product team member for the organization’s Transfusion Medicine regulatory team. + Supports necessary regulatory activities required for product market entry/launch and on-market support of transfusion medicine assay support. + Compile, prepare, review and submit on-market regulatory submissions to authorities. + Work with cross functional teams to review and approve protocols to ensure alignment with regulatory requirements. + Strategic Planning: Assist in SOP development and review. Provide regulatory input to product lifecycle planning. Continue to revisit and compare regulatory outcomes with initial product concepts to make recommendations on future actions. Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes. + Understand, investigate and evaluate regulatory history/background of class, disease/ therapeutic/diagnostic context in order to assess regulatory implications for approval. Determine trade issues to anticipate regulatory obstacles. Determine and communicate submission and approval requirements. Participate in risk-benefit analysis for regulatory compliance. + Compile; prepare; review and submit regulatory submission to authorities (domestic and international) with supervision. + Monitor impact of changing regulations on submission strategies. Monitor applications under regulatory review. Monitor and submit applicable reports to regulatory authorities. Evaluate proposed manufacturing changes for regulatory filing strategies. Negotiate and interact with regulatory authorities during the development and review process to ensure submission approval. + Post market: Maintain annual licenses, registrations, listings and patent information. Assist compliance with product post marketing approval requirements. + Review and approve advertising and promotional items to ensure regulatory compliance. 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. Analyze the input of cumulative product changes to current product submissions. + 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. + Participates as a Team Member: Actively contributes to the team process, commits to team goals, expresses opinions and shares ideas freely. + Contributes to the creation of the team's mission objectives and strategies, accepts team decisions and works toward their implementation. **Required Qualifications** + Bachelor's degree in related field or an equivalent combination of education and work experience + 3-4 years' experience in a regulated industry (e.g., medical products, nutritional's) **Knowledge of:** + Regulatory history, guidelines, policies, standards, practices, requirements and precedents + Regulatory agency structure and processes + Principles and requirements of applicable regulations and agency guidance + Submission/registration types and requirements + IVDR Technical Documentation for Class D products + CBER submissions for biologic products (BLA, CBE/CBE-30, PAS) + GxPs (GCPs, GLPs, GMPs) + Principles and requirements of promotion, advertising and labeling + Ethical guidelines of the regulatory profession **Preferred Qualifications** + Masters in Regulatory Affairs preferred and may be used in lieu of direct regulatory experience + 2-3 years of experience in regulatory industry but may consider quality assurance, research and development/support, scientific affairs, operations, or related area + Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Apply Now (https://www.jobs.abbott/us/en) **Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx) 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 $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com