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Related keywords
- Marketing Leader Latin America
- Regulatory Affairs Manager
- Latin America Resupply Csr
- Food Regulatory Affairs Manager
- International Regulatory Affairs Manager
- Latin America Research Manager
- Sr Manager Sales Latin America
- Regulatory Affairs
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- Latin America Marketing Manager
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Regulatory Affairs Manager (Latin America) - Nutrition - Abbott Park, Il
Company | Abbott |
Address | Illinois, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-07-25 |
Posted at | 11 months ago |
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 115,000 colleagues serve people in more than 160 countries.
- 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 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 stability of a company with a record of strong financial performance and history of being actively involved in local communities
- Company Paid Pension Plan
- Financial security through competitive compensation, incentives and retirement plans
- Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1
- 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.
- 401(k) retirement savings with a generous company match of 5%
- Training and career development, with onboarding programs for new employees and tuition assistance
- Vacation – 3 weeks accrued vacation (1st yr. is prorated) + vacation buy program + 3 personal days + 10 paid holidays
- Identifying and obtaining documents needed and ensuring that they are effectively presented for the registration of the products.
- Analyzing and identifying regulatory requirements against project needs
- Preparing options, suggestions, and/or a regulatory assessment for product
- Communicating registration needs prior to and during product development
- Assist in the development of regional regulatory strategies and update strategies based upon regulatory changes.
- Assist with label review for compliance
- Review and approve Reginal advertising and promotional items to ensure regulatory compliance
- Provide regulatory input for product action and related communications
- Provide regulatory input to product lifecycle planning
- Monitor impact of changing regulations on submission strategies
- Submit and review change controls to determine the level of change and consequent submission requirements
- Determine and communicate submission and approval requirements
- Monitor applications under regulatory review
- Participate in risk evaluation analysis for regulatory compliance
- Continue to revisit and compare regulatory outcomes with initial product concepts to make recommendations on future actions
- Minimum 3 years of prior team leadership and talent development experience along with budgetary responsibility.
- 15+ years of deep expertise in analytical chemistry research, food & physical chemistry, method development, and troubleshooting with food and beverage products.
- Strong understanding of GLP, ISO 17025, and other laboratory quality requirements.
- Proficient with basic computer skills, including word processing, spreadsheets, presentations, and lab information systems.
- Team oriented, with high energy and desire to achieve results. Ability to work in multidisciplinary teams and meet business goals.
- BA/BS + 10 years, MS + 7 years, or PhD in Analytical Chemistry, Food Science, or equivalent with a background in method development and validation.
- Excellent written and verbal communication skills to communicate with technical and commercial stakeholders the full relevance of scientific observations and to produce documents and reports. Strong organizational skills required.
- Fluency in Spanish and English.
- Note: Higher education may compensate for years of experience.
- Minimum Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology, nutrition, food science, etc.) or medical fields is preferred plus 5 years of experience in a regulated industry (e.g., medical products, nutritionals).
- Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)
- 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
- 10% travel
- Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
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