USP

Support to reaction monitoring, scale up and final analysis of samples as per monograph, in-house procedures including method development if required. Prepare development reports for Synthetic Support projects. Involve in project acceptance. Execute projects per the approved test protocols if assigned.

This is a non-supervisory position to support development of Reference materials. The successful applicant in this role will work on projects including Analytical Method Development for in process samples for synthetic lab.

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.

Develop, optimize, and publish high-quality analytical methods using high-field NMR and qNMR applications; publications may include white papers, application notes, or journal articles ; Acquire high resolution qNMR spectra and implement structural elucidation for obtaining chemical structural information to develop QM spectral analysis models

In this role, the Senior Scientist-I will work on isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical technique. Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects.

This is a non-supervisory position in the Compendial Development Laboratory within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP, NF monographs and maintaining safety and a GLP environment in the lab. Prepare and review project plans, reports, laboratory notebooks/Laboratory Management System LMS, and compile project data as required. Masters Degree in Chemistry Analytical/Organic or Pharmaceutical Sciences

Responsible for timely preparation of collaborative testing protocols for new/replacement RS lots, technical assistance for collaborating labs. To review the analytical data received from the Collaborators and to prepare summary reports and RSCEP packages, preparation of packaging and QC testing instructions and assigning periodic re-test intervals.

Must have hands on experience in working with chemical methods and handling instruments like Prep HPLC and HPLC. Expertise in HPLC & Prep HPLC method development and basic undersatnding in data interpretation of various analytical technique such as LCMS, GCMS, FTIR, UV-Visible, NMR etc is required.

Demonstrates a robust scientific approach to laboratory analysis. Regularly utilizes personal experience, academic training, and technical insights, including emerging sciences, to address complex technical issues within the laboratory.