USP is proud to be an equal opportunity/affirmative action employer. Employment selection and related decisions are made without regard to sex, gender identity, race, age, disability, religion, national origin, color, veteran status or any other protected class. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
Post : Scientist III - Reference Standard Laboratory
• 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 Equipments 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.
• Ph.D. in Chemistry or master’s degree in chemistry or Pharmacy.
• 1 to 2 years with relevant laboratory experience for Ph.D. candidates.
• 5 to 7 years with relevant laboratory experience for master’s degree candidates.
• 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, GC, IC and troubleshooting, proficient in other related analytical instrumentation (Mass Spectrometry, Titration, IR, KF, UV, Thermal, Elemental analysis by ICP 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, Lab Management System and Electronic Laboratory Notebook, 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.
Experience : 1-5+ years
Qualification : M.Pharm, MSc or Ph.D
Location : Hyderabad
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Reference Standards Laboratory
End Date : 30th May, 2021
See All Other Jobs in our Database