U.S. Pharmacopeial Convention (USP)
Scientist II, RSL
Hyderabad, India
Description
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 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.
Basic Qualifications
·
Ph.D. in Chemistry with 1-2 years or
Master degree in Chemistry with 4-6 years of relevant laboratory experience.
Preferred
Qualifications
· 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 and troubleshooting, proficient in other related analytical instrumentation (Titrations, IR, KF, UV, Thermal, Elemental analysis 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, ELN, 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.USP offers an impressive benefits
package, including:
· Comprehensive individual and
family health insurance plans
· Annual Master Health check-up
plans
· Generous paid holidays, vacation
leave
· Transportation services for office
commute.
The U.S. Pharmacopeial Convention
(USP) is a scientific nonprofit 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.
Being a part of USP means belonging
to a diverse culture made up of more than 1,000 talented professionals working
together at five international locations. We share our expertise in science,
IT, human resources, quality assurance, communications, administrative
management, and more...all to support an overall mission dedicated to making a
difference by providing standards and programs that help improve the quality of
medicines, dietary supplements, and foods worldwide.
USP is proud to be an equal
employment opportunity employer (EEOE) and affirmative action employer.
Employment selection and related decisions are made without regard to sex,
race, age, disability, religion, national origin, color, veteran status, sexual
orientation, gender identity or any other protected class. We are committed to
working with and providing reasonable accommodation to individuals with
disabilities.
Job
Category Chemistry & Scientific
Standards
Job Type Full-Time
For more information and online application click here
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