Manager, Regulatory Affairs

Follow your aspirations to Abbott for diverse opportunities, competitive salaries, great benefits, a 401(k) retirement savings plan, a company paid pension plan and profit sharing, all with a company providing the growth and strength to build your future.
1. Manage regulatory projects and provide regulatory and technical oversight to ensure timely submission and approval of CMC dossiers.2. Effectively influence other functional areas to execute projects within area of responsibility.3. Provide regulatory, compliance advice, consultation and support to Abbott's Pharmaceutical business units.4. Manage change in compliance with applicable global regulations.5. Identify regulatory CMC risks/opportunities for projects in area of responsibility and propose strategies to address risks.The individual is expected to work independently in these functions.6. Manage and provide oversight for regulatory relationships with Agency counterparts or Area groups within the scope of responsibility. The individual is expected to work mostly independent in this function.Qualifications
BS, MS, or PhD in Pharmaceutical Sciences, Chemistry, Engineering or related field.Minimum three years of experience in a CMC technical position within R&D, Manufacturing Sciences, Quality Assurance and/or Regulatory Affairs.

${abbott.description.certifications}Abbott welcomes and encourages diversity in our workforce. EEO/AATo apply for this position, click on the Apply Now buttonTo learn more about Abbott and view other opportunities, please visit: http://www.abbott.com/career/career_center.cfm
REQUIREMENTS
Please see Job Description