Support reaction monitoring, scale-up and final analysis of samples as per monograph /in-house procedures including method development/validation if required. Prepare development reports for Synthetic Support projects. Execute projects per the approved test protocols if assigned.
Plan, execute, and complete the projects as per specifications, timelines, and budget.
Responsible for preparation and review of SOPs, protocols, reports, etc.
Ensure project requirements by coordinating with external vendors and all internal relevant departments.
Responsible for ensuring the required maintenance and calibrations of the equipment
Responsible for preparing, executing and completing IQ/OQ/PQ of new instruments as assigned
Preparation and planning for ISO-9001 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues in a timely manner.
Qualification & Expeirence
Sc. in Analytical Chemistry / Organic Chemistry/M. Pharm, having 8-10 years of experience in Analytical Research and Development or Ph.D. with 4-7 years of experience in Analytical Research and Development.
Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, LC-MS, GC-MS, FTIR, UV-Visible, wet chemistry, etc.