Senior Scientist I, Bioanalytical
Posted Apr 7, 2026
Key Responsibilities:
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Demonstrate laboratory skills in analytical Chromatography (HPLC/UPLC/Ion-chromatography), Capillary Electrophoresis, SEC-MALS, Circular-dichroism, and Mass-spectrometry for qualitative and quantitative experiments. - Perform various studies such as Intact Mass, Peptide mapping, Glycan profiling, HMW & LMW, HCP, Impurity Profiling, and PTM analysis. - Plan and execute Compendial and R&D projects, including proof of concept studies in Biologics. - Evaluate scientific reports, troubleshoot and solve problems in the laboratory, and mentor team members. - Engage in project coordination with cross-functional/global teams, prepare project reports and SOPs, and ensure compliance with USPs Quality Management System. - Assist in laboratory/project management improvements and participate in Internal audits, ISO 9001, and ISO 17025 audits. Qualifications Required:
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Ph.D. degree in Biochemistry, Analytical Chemistry, or Biological Sciences with 7-10 years of relevant work experience, or MSc./M.Tech./M.Pharm. with 8-13 years of industry experience in Analytical R&D and QC department of Biopharmaceutical industry. - Experience in method development, validation, technology transfer, and analytical characterization for biomolecules. - Strong technical knowledge in peptides and mAbs or CGT and Vaccines area, cGLP/cGMP environment, and reference standards development. - Desired preferences include proficiency in operating and troubleshooting analytical instruments, familiarity with QMS systems, technical writing, communication, and presentation skills. Note: USP is an equal employment opportunity employer committed to inclusivity and diversity. Role Overview: At USP, you will be joining a scientific nonprofit organization dedicated to setting standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements worldwide. As a Bioanalytical Scientist, you will play a crucial role in executing bioanalytical projects, collaborative testing of reference standards, and contributing to verification and development programs. Key Responsibilities: