U.S. Pharmacopeial Convention (USP) Hiring Scientist III - Reference Standard Laboratory Apply Now
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 Leader 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 troubleshoot the scientific aspects of the
projects on need basis.
Responsible
for preparation and review of SOPs, 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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