At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 94,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. Please note that candidates need to be eligible to work in the U.S. without Abbott sponsorship.
Position requires expertise in molecular biology and immunology in order to support qualification and validation activities for analytical methods and equipment within a GLP environment.
Perform qualifications of analytical method standards and controls through use of ELISA, SDS-PAGE, and other techniques to support food safety-related allergen control measures as well as production of hypoallergenic infant formula.
Ensure accuracy and precision of data generated by analytical methods.
Design experiments, author protocols, and introduce new technologies to further characterize proteins and DNA within broad scope of business interests
Stay up-to-date on changing global positions for analytical requirements related to allergens, gluten-free, and GMO labeling standards.
Summarize and report results to internal stakeholders including quality assurance, regulatory affairs, medical safety and R&D teams
Interface with internal and external stakeholders including key opinion leaders within the allergen field and present data