Apply for Scientist – Verifications Programs @ U.S. Pharmacopeial Convention (USP)

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Job Title : Scientist I/II, Verification Programs

Tracking Code : 887-679

Job Description

This is a non-supervisory position in Verification Programs department, responsible for performing the required tests as a part of the projects and maintaining GLP environment in the lab.

Roles and Responsibilities:

  • Execute the analytical tests allotted by team leader.
  • Complete the projects as per the project timelines and priorities.
  • Compilation of project reports and response to QA observations.
  • Ensure the implementation of GLP, safety systems in the labs.
  • Ensure the calibration of the equipment’s as per the schedules.
  • Indent chemicals, column, Glass ware and other project requirements and their procurement by coordination with lab operation and purchase department in advance keeping in mind the project deadlines.
  • Ensure and follow USP mission, policies and procedures.
  • Maintain good relationship with RSL, PQM, Lab Operations and other departments.
  • Preparation, executing and completing IQ/OQ/PQ of new instruments.
  • Preparation and planning for ISO-9001 & ISO- 17025 certification/recertification by participating actively, verification of protocols and related documents and take an active role in the internal as well as external QA audits and address the audit issues on a timely manner.
  • Taking up any other additional responsibilities assigned by supervisor on a proactive basis and allotting additional responsibilities to the reporting staff in consultation with the supervisor.

Required Skills

  • Must have hands on experience in working with chemical methods and handling instruments like HPLC, GC, Dissolution, ICP, FTIR, UV-Visible, etc.
  • Familiarity with and exposure to external regulatory audits required. Working knowledge of computer applications, such as MS Word and MS Excel and exposure to lab software’s such as Empower , e-LNB and NuGenesis, would be advantageous.
  • Prior experience of Formulation and Dietary supplements analysis in a high volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus.
  • Must be able to communicate effectively with customers.

Required Experience

Masters in Pharmaeutical Sciences (M.Pharm) Or Master’s Degree in Chemistry (Organic/ Analytical Chemistry) with 1-5 years hands on experience in the field of analytical testing of pharmaceutical substances, finished products and Dietary Supplements.

Job Location : Hyderabad, Andhra Pradesh, India

Position Type : Full-Time/Regular

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