About AbbottAbbott is a global healthcare leader, creating breakthrough science to improve people's health.We're always looking towards the future, anticipating changes in medical science and technology.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 will have access to:Career development with an international company where you can grow the career you dream of .Excellent benefits package with family healthcareA 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.Primary Functions: Establish effective working relationships with Third Party Manufacturers (TPM), Commercial and Abbott Nutrition Supply Chain (ANSC) Divisional functions including Regulatory, Medical, Tech Centre and Quality to provide support for product moves and New Product Introductions.A logical thinker, the R&D Associate will bring a technical and scientific expertise to all matters pertaining to the delivery to market of new powder and liquid nutritional products which are produced at Third Party Manufacturers in Asia and Europe.An 'innovation oriented' contributor with excellent attention to detail and communication skills, the R&D Associate will have the ability and inquisitiveness to comprehend the details behind processes and transactions beyond his/her direct area of responsibility to ensure compliance to both regulatory and product design requirements.Scope Includes:Product DevelopmentDesign new products or variations of existing products.Design and re-formulate existing nutritional products for manufacture at TPM sites to meet new regulations or to meet new market requirements.Formulate new premixes.Support the qualification of new ingredients, including premixes, and suppliers.Support the supplier audits as required Support the development of manufacturing processes for the manufacture of new and existing products at the various TPMs.Documentation Development Draft new document packages for new list numbers/list number FE's Revise existing documentation as needed.Create Raw Material Specification documents for new ingredients and advise QA on Raw Material testing Program requirementsCreate protocols for investigation and stability activity.Prepare Deviations in the Quality Systems to support First Lot To Stock manufacture.Technical ExpertiseSupport assessment of new suppliers and ingredients.Assess inherent data from ingredients and adjust formulations as necessary Draft finished product testing requirements Identify new testing requirements and premix markers.Create special documentation as required to support registrations Investigations for alternate claims.Provide supplemental information to Market Affiliates, Medical Safety and Regulatory Affairs Troubleshoot formulation and manufacturing issues Support QA function of the TPM group with investigation of complaints, deviations and Exceptions Reports.Project ActivitiesSupport the development of project scope, trial and budget requirements.Develop test plans and test requirements through the life cycle of the product.Attend project meetings for all R&D activities with the project team and the TPM(s) and provide technical leadership to multi-disciplinary project teams to develop several products in parallel.Stability Data Maintain repository of stability data for TPM products.Be accountable to identify, cost-out and oversee product testing and stability program requirements for existing products, new product placements and strategic resourcing initiatives .Education : BSc in food science or engineering preferredExperience : Minimum of 3 to 5 years of prior experience in formulation and manufacturing processes of powder and liquid nutritional products in the Nutritional industryTravel: Estimate at 20%
