7 Uvvisible Jobs

You will be responsible for leading the characterization of peptides and small molecules using Liquid Chromatography and High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) to determine structural elucidation and impurities profiling. As a Team Lead, you will manage a team focused on Peptide / Protein characterization through HRMS. Your duties will include method development, impurity profiling of Peptides/Proteins, and Impurities characterization using HRMS. Additionally, you will utilize spectroscopy (UV-Visible, Circular Dichroism, Spectrofluorometer), Capillary Electrophoresis, and analytical method development for characterization purposes. - Handling LC-HRMS for Characterization of P...

As a Scientist I at the U.S. Pharmacopeial Convention (USP), you will play a crucial role in supporting the development of Reference materials. Your responsibilities will include: - Supporting reaction monitoring, scale up, and final analysis of samples as per monograph/in-house procedures, including method development if required. - Preparing development reports for Synthetic Support projects and being involved in project acceptance. Executing projects per approved test protocols when assigned. - Preparing, executing, and completing IQ/OQ/PQ of new instruments. Indenting the required glassware, chemicals, and columns for the ARD projects. Maintaining GLP and implementing safety procedures w...

Role Overview: As a Scientist II at USP, you will play a crucial role in supporting the development of reference materials, specifically focusing on analytical method development for in-process samples in the synthetic lab. Your responsibilities will include performing various analytical tests, ensuring a safe and GLP-compliant environment in the lab, evaluating reference standards, developing and validating official methods, conducting stability studies, and contributing to research projects within the analytical department. Key Responsibilities: - Support reaction monitoring, scale up, and final analysis of samples based on monograph/in-house procedures, including method development when n...

The Assistant Manager - QC position at Bharuch SEZ requires a candidate with complete experience in API/Bulk/Intermediates industries as per global regulatory requirements. The individual will be responsible for the implementation and compliances of 21CFR-Part11, ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP, and other global QMS requirements at the SEZ site. Key responsibilities include regularizing QC activities as per cGMP requirements, ensuring regulatory and pharmacopeia compliance in the lab, reviewing hybrid and electronic data for IPQC and FG analysis, conducting analytical method validation, OOS, and OOT. The candidate should have knowledge about IMS system, analytical skills for QC ...

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to r...

At USP, inclusive scientific collaboration is highly valued, recognizing the importance of diverse expertise in strengthening the development of trusted public health standards. The organizational culture at USP supports equitable access to mentorship, professional development, and leadership opportunities, reflecting the belief that broad participation in scientific leadership leads to more impactful global health outcomes. As an equal employment opportunity employer, USP is committed to fair, merit-based selection processes that enable the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Reasonable accommodations are provided to...

At USP, we highly value inclusive scientific collaboration and acknowledge that attracting diverse expertise strengthens our ability to develop trusted public health standards. We cultivate an organizational culture that supports fair access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research embody our belief that ensuring broad participation in scientific leadership leads to stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is dedicated to ensuring fair, merit-based selection processes that enable the best scientific minds - regardless of background - to co...