The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,100 hardworking professionals across five global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.
Post : Scientist II, Reference Standard Laboratory
Brief Job Overview
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.
Job 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, sample archival 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 troubleshoot 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.
Candidate Profile
• Masters degree in chemistry or Pharmacy.
• 5 to 7 years with relevant laboratory experience.
• 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, and troubleshooting, proficient in other related analytical instrumentation (Titration, IR, KF, UV, wet analytical techniques 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 experience on Empower software is required.
• Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D or a contract pharmaceutical analytical laboratory testing organization is a plus.
Additional Information
Experience : 5 to 7 years
Qualification : M.Pharm or MSc
Location : Hyderabad
Industry Type : Pharma
Functional Area : RSL
End Date : 15th April, 2023
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