US Pharmacopeia Hiring Scientist I, Verification Programs Master’s degree in Pharmacy or Analytical chemistry Apply Now
Roles and Responsibilities:
Executes the Verification
projects by performing individual analytical tests allotted by the Group
Leader.
Completes the projects as per the project timelines and
priorities.
Demonstrates solid scientific approach to analysis in the
laboratory.
Routinely applies personal experience, academic training, and technical
insights – including emerging sciences – to solve complex technical problems
within the laboratory;
Compiles project reports and responds QA observations.
Executes all testing and analysis of data with excellence and
essentially no errors.
Demonstrates a strong desire to continue learning and grow
personal capability.
Pursues, recommends, and implements new approaches or processes to
improve laboratory operations.
Positively influences project direction by ensuring own work is
congruent with overall direction of laboratory projects.
Assists with other testing programs and housekeeping duties in the
laboratory as needed.
Ensures the implementation of GLP, safety systems in labs.
Ensures the calibration of the equipment as per the schedule.
Indents chemicals, columns, Glassware, etc. and procures them by
coordinating with lab operations and purchase department in advance keeping in
mind the project deadlines.
Ensures and follows USP mission, policies and procedures.
Maintains good relationship with QA, HR, Purchase, accounting, IT
and other dept.
Preparation and planning for ISO-9001 & ISO- 17025
certification/recertification by participating actively and take an active role
in the internal as well as external QA audits and address the audit issues in a
timely manner.
Supports collaborative testing, GPH, RSL and other departmental
teams in terms of project testing, review, execution and approval whenever
needed.
Education:
Master’s degree in pharmacy
or Analytical chemistry.
Experience:
Minimum 1 to 3 years of
relevant laboratory experience.
Required Skills
Ability to lead projects to completion with a high degree of
scientific expertise. Proficient with pharmaceutical testing requirements and
test protocols involving compendial methods (USP, BP, EP, etc.). Expert in
ICP-OES, HPLC, GC,ICP-MS,LC-MS, Dissolution analysis and troubleshooting,
proficient in other related analytical instrumentation (IR, KF, UV, etc),
strong communication and presentation skills, both verbal and written,
experience working in the pharmaceutical industry strongly preferred. Knowledge
of DEA, ICH guidelines and FDA regulations, and experience with compendial
procedures and compliance strongly preferred. Proficiency with electronic
documentation systems strongly preferred. Takes personal responsibility to ensure
work is delivered on time and is the highest possible quality. Skills to
anticipate, troubleshoot, and solve technical problems.
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