Scientist II, Bioanalytical The U.S. Pharmacopeia (USP)

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

At USP, inclusive scientific collaboration is highly valued as it is believed that diverse expertise enhances the development of trusted public health standards. The organizational culture at USP promotes equitable access to mentorship, professional development, and leadership opportunities to ensure broad participation in scientific leadership for stronger and more impactful outcomes in global health. As an equal employment opportunity employer (EEOE), USP is committed to fair, merit-based selection processes that allow the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Accommodations are provided to individuals with disabilities, and policies are upheld to create an inclusive and collaborative work environment. The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for medicines, food ingredients, and dietary supplements worldwide. USP's drug standards are enforceable in the United States by the Food and Drug Administration and are utilized in over 140 countries. The position offered is a hands-on, non-supervisory role where the incumbent will apply their knowledge and practical experience in executing bioanalytical projects on collaborative testing of reference standards, documentary standards, and characterization of biological products. The individual will also engage in verification, international and national reference standard development programs as assigned. In this role, you will have the opportunity to contribute significantly to increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. The ideal candidate for this position will possess a postgraduate degree in a relevant stream of Biological Sciences along with 3-6 years of industry experience in Analytical R&D and QC departments of the Biopharmaceutical industry. Experience in method development, validation, and technology transfer, along with analytical characterization for biomolecules, will be advantageous. A strong background in cGLP/cGMP environments and expertise in specific analytical techniques are desired. Key responsibilities include aligning with USP's mission, demonstrating laboratory skills in various analytical techniques, executing experiments, analyzing data, contributing to projects, engaging in project coordination, preparing reports and documents, and continuously improving laboratory/project management methods and processes. USP is looking for a candidate who not only meets the technical requirements but also demonstrates excellent communication, presentation, and technical writing skills. Proficiency in using an Electronic Laboratory Notebook (ELN) is preferred along with strong written and verbal communication abilities. As an organization, USP provides comprehensive benefits to ensure the personal and financial well-being of its employees and their families. The company values inclusivity, diversity, and equity, and is dedicated to creating a work environment that fosters growth, mentorship, and professional opportunities for all its employees.,

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