Job Description

Description Executing the analytical tests allotted by Project or Group Leader.

• Verification of test protocol and giving test kit approvals, if required.

• Supporting Verification, GPH, PQM, stability and other departmental

teams in terms of testing and project review whenever needed.

• Responsible for preparation of project evaluation reports.

• Responsible for sample tracking and chemical inventory tracking in the laboratory.

• Coordination with group leader to ensure completion of the projects allotted to the

team.

• Initial review of the project reports and documents and assisting the group leader

when required.

• Completing the project as per the timelines and trouble shoot the scientific

aspects of the projects on need basis.

• Responsible for preparation and review of SOP’s, protocols, reports etc.

• Responsible for performing the calibration of the equipment as per the schedule.

• Responsible for preparing, executing and completing IQ/OQ/PQ of new

instruments.

• Ensuring that the chemicals and column etc. are available for the

projects and forward the purchase requisitions.

• Taking up any additional responsibilities assigned by group leader from time to

time.

• Ensure all lab safety and GLP practices are maintained in the lab and participate

actively in the internal and external audits and certification Basic Qualifications: Ph.D. in Chemistry with 1-2 years or master’s degree in chemistry with 3-5 years of relevant laboratory experience. Preferred Qualifications: Proven track record of consistently delivering projects on time and with high quality. Proficient with pharmaceutical testing requirements and test protocols involving compendial methods for reference materials (USP, FCC, NF, etc.). Expert in Chromatographic analysis, especially in HPLC and troubleshooting, proficient in other related analytical instrumentation (Titrations, IR, KF, UV, Thermal, Elemental analysis etc.), Takes personal responsibility for delivery of projects to customers. Ability to embrace and lead change. Extremely adaptable. Excellent communication skills, both written and verbal. Having knowledge of Empower software, ELN, ERP, QR coding system are added advantages. Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus. Supervisory Responsibilities None Benefits USP provides you with the benefits you need to protect yourself and your family today and tomorrow. From company-paid time off, comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial wellbeing are protected. About USP The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP brings together more than 1,100 talented professionals across five global locations to deliver its mission to strengthen the supply of safe quality medicines and supplements worldwide. USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. Employment selection and related decisions are made without regard to sex, race, age, disability, religion, national origin, color, veteran status, sexual orientation, gender identity or any other protected class. We are committed to working with and providing reasonable GHR Doc 3.Version 5 - 5/Nov/2021 G:\01 Employment\01a Global TA Controlled Documents accommodation to individuals with disabilities. USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP. Job Category Chemistry & Scientific Standards Job Type Full-Time