.Development & Methods Validation Chemist, Ocoyoacac Location: Ocoyoacac Toluca About the jobWe deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Development & Methods Validation Chemist within our Support to projects and operations, will be to manage new projects in the area of analytical development proposing, while developing, optimizing and validating analytical methods in Industrial Development and Technology.At Sanofi Consumer Healthcare, we build trusted and loved brands that connect with hundreds of millions of consumers worldwide. Our ambition is to enable better self-care for individuals and communities, while also contributing to a healthier planet. To achieve this, we need people who can shape the future of our business and help us on our journey to becoming the best fast-moving consumer healthcare company in and for the world.Main responsibilities:Management of out-of-spec resultsPerform analysis of samples, stabilities, developmentValidation of analytic methodsTransfer of analytic methodsStatistical analysis of trendsProject management of brands of Sanofi CHCFollow up on activities with third parties and externalsActivity reportingFollow up of protocolsAbout youBachelor Degree in pharmacy, chemical or biological pharmacy, biology, biomedicine or related fields.At least 3 years experience in methods for development and validationExperience in a control quality laboratory in the pharmaceutical industryExperience in development and chromatography analysisExperience in HPLC ChromatographyExperience in managing technical and specialized reportsUpper intermediate to advanced EnglishAbility to work with little supervisionAlikeness to work in fast paced environmentsKnowledge of Guidelines NOM-073-SSA1, Stability NOM-177-SSA1Knowledge in Quality Guidelines ICH: Q2 Analytical Validation, Q6A- Q6B Specifications, Q3A - Q3D Impurities, Q1A - Q1F Stability, Q8 Pharmaceutical Development, Q12 Lifecycle Management.Why choose us?Bring the miracles of science to life alongside a supportive, future-focused team.Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs.Being able to work in a world class company with ultimate standards in health, safety and environment.Pursue Progress. Discover Extraordinary
