Opportunity for M.Pharm or MSc as Scientist at U.S. Pharmacopeial Convention- Apply before November 15, 2023

U.S. Pharmacopeial Convention

Website U.S. Pharmacopeial Convention

About U.S. Pharmacopeial Convention

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that works in collaboration with leading health and science authorities from around the world. Its primary objective is to establish quality standards for medicines, dietary supplements, and food ingredients. USP’s core belief is that Equity equals Excellence, and this belief is reflected in their fundamental value of having a Passion for Quality. This dedication to quality is upheld by their team of over 1,100 diligent professionals spread across five global locations. Their collective mission is to enhance the availability of safe and high-quality medicines and supplements on a global scale.

Job Post: Scientist I, RSL

Job Overview

Position at U.S. Pharmacopeial Convention: Scientist I, Reference Standard Laboratory (RSL)

Responsibilities at U.S. Pharmacopeial Convention : Ensuring GLP Compliance and Conducting Pharmaceutical Analysis

Roles and Responsibilities

  • Analytical Testing: Perform tests as assigned by Project or Group Leader.
  • Test Protocol Verification: Verify test protocols and approve test kits if necessary.
  • Supporting Teams: Assist Verification, GPH, PQM, stability, and other departmental teams with testing and project reviews as required.
  • Project Reports: Prepare project evaluation reports.
  • Sample Management: Responsible for sample tracking, archival, and chemical inventory in the laboratory.
  • Project Coordination: Coordinate with the group leader to ensure project completion.
  • Project Review: Initial review of project reports and documents, assisting the group leader as needed.
  • Timely Project Completion: Ensure projects are completed according to timelines and troubleshoot scientific aspects as necessary.
  • Documentation: Prepare and review SOPs, protocols, and reports.
  • Equipment Calibration: Perform equipment calibration as per the schedule.
  • Instrument Validation: Prepare, execute, and complete IQ/OQ/PQ of new instruments.
  • Supply Management: Ensure availability of chemicals and columns for projects, and initiate purchase requisitions.
  • Additional Tasks: Take on extra responsibilities as assigned by the group leader.
  • Safety and Compliance: Maintain lab safety and GLP practices, actively participate in internal and external audits and certification.

Candidate Profile

  • Education: Master’s degree in chemistry or pharmacy.
  • Experience: 1 to 3 years of relevant laboratory experience for Master’s degree candidates.
  • Expertise: Proficient in HPLC with Empower software, wet analytical techniques, and troubleshooting.
  • Industry Experience: Previous experience in a reputable organization with API material testing.
  • Pharmaceutical Knowledge: Proficient in pharmaceutical testing requirements.
  • Communication Skills: Strong written and verbal communication skills.
  • Analytical Techniques: Proficiency in other analytical techniques like GC, IC, Mass Spectrometry, Thermal, and Elemental analysis by ICP.
  • Test Protocols: Familiar with test protocols involving compendial methods for reference materials (USP, FCC, NF, etc.).
  • Additional Skills: Knowledge of Lab Management System and Electronic Laboratory Notebook, ERP, and QR coding system is advantageous.

Additional Information

  • Experience Required at U.S. Pharmacopeial Convention: 1 to 3 years
  • Qualification Required at U.S. Pharmacopeial Convention: Master’s degree in chemistry or Pharmacy
  • Location: Hyderabad
  • Industry Type: Pharma / Healthcare / Clinical research
  • Application Deadline: November 15, 2023
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To apply for this job please visit usp.jobs.