The U.S. Pharmacopeial Convention (USP) Scientist III Hyderabad
The U.S. Pharmacopeial Convention (USP) is a scientific
non-profit organization that sets standards for the identity, strength,
quality, and purity of medicines, food ingredients, and dietary supplements
manufactured, distributed and consumed worldwide. USP’s drug standards are
enforceable in the United States by the Food and Drug Administration, and these
standards are used in more than 140 countries.
USP promotes Diversity & Inclusion at Workplace and
encourages Equal Employment Opportunity and Affirmative Action
Summary of the Position
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.
Roles and
Responsibilities
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 archival, 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.
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