The
U.S. Pharmacopeial Convention (USP) Hiring Scientist II (Bioanalytical) –
Biologics M.Sc./M. Tech./M. Pharm. Apply Now
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 hands-on, non-supervisory position in which the incumbent applies their
knowledge and practical experience in execution of bioanalytical projects on
collaborative testing of reference standards, documentary standards and
characterization of biological products. Additionally, the incumbent will also
actively engage and contribute in verification, international and national
reference standard development programs as assigned.
Roles
and Responsibilities
Aligns
with USP’s mission, goals and objectives; complies with USP’s guidelines and
other requirements.
Plans
and executes Compendial, Verification and R&D projects for product classes
such as proteins, monoclonal antibodies, peptides, antibiotics and any other
biological products as assigned.
Prepare
project reports as per USP’s quality systems and procedures.
Demonstrates
strong skills and expertise in Bioanalytical methods in the areas of
Chromatography, Colorimetric assays, Electrophoresis & Mass spectrometry.
Routinely
applies personal experience, academic training, and technical insights to
troubleshoot and solve problems in the laboratory.
Complies
with USP’s Quality Management System and assists group leaders in implementing
process improvements.
Performs
other duties as assigned.
Required
Skills
Basic
Qualifications
M.Sc./M.
Tech./M. Pharm. in relevant stream of biological sciences with 4-6 years of
relevant experience in working with biologics product class.
Experience
should include strong technical knowledge and practical experience in
Bioanalytical area.
Work
experience in cGLP/cGMP environment is desirable.
Required
Experience
Preferred
Qualifications
M.Sc.
(Biochemistry / Biotechnology)/ M. Tech (Biotechnology / Bioprocess
engineering)/ M. Pharm with expertise on techniques like HPLC, UPLC,
Colorimetry, Spectrophotometry & Electrophoresis (IEF, SDS-PAGE, Western
Blot)
Expertise
in Mass Spectrometry (Characterization/Quantification) & Capillary
Electrophoresis would be preferred.
Understanding
of QMS along with good communication skills is a must.
Ability
to plan, design, execute, trouble shoot, and resolve technical issues within
the scope.
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