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Opportunity to work as RSL Scientist at U.S. Pharmacopeial Convention – Apply before 05th May 2025

U.S. Pharmacopeial Convention (USP)
Pharmacareer

Website U.S. Pharmacopeial Convention (USP)

About USP

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that sets quality standards for medicines, dietary supplements, and food ingredients globally. With over 1,300 dedicated professionals across twenty countries, USP is driven by its core value—Passion for Quality—to promote equity and excellence in health. Our mission is to ensure the global supply of safe and effective medicines and supplements.

Position Summary

We are seeking a Scientist II to join our Reference Standard Laboratory (RSL) team in Hyderabad. This is a non-supervisory role focused on executing analytical testing, supporting project timelines, and ensuring compliance with Good Laboratory Practices (GLP). The ideal candidate will be technically sound in pharmaceutical analysis and committed to quality and lab excellence.

Key Responsibilities

  • Perform analytical testing assigned by Project or Group Leaders.

  • Support project completion by troubleshooting scientific and operational challenges.

  • Maintain sample and chemical inventory; manage sample archival and tracking.

  • Ensure timely calibration of laboratory equipment and initiate purchase requests as needed.

  • Contribute to the installation and qualification (IQ/OQ/PQ) of new instruments.

  • Prepare and review Standard Operating Procedures (SOPs), protocols, and reports.

  • Provide technical review of project documents and assist with report finalization.

  • Maintain GLP and safety practices in the lab; participate in internal/external audits.

  • Adhere to Quality Management System (QMS) protocols and manage deviations/incidents.

  • Collaborate with cross-functional teams including Verification, GPH, PQM, and Stability for project support.

Candidate Profile

Educational Qualification:

  • M.Sc. (Analytical or Organic Chemistry) or M.Pharm (Pharmaceutical Sciences/Analysis)

Experience:

  • 3 to 6 years of relevant laboratory experience in pharmaceutical testing (API/formulations)

Technical Competencies:

  • Strong hands-on expertise in HPLC and GC instrumentation

  • Skilled in using lab instruments: KF, FTIR, UV, Titrators, SOR, Thermal equipment, TLC, Elemental Analyzer

  • Experience in wet chemical analysis techniques

  • Proficiency in Empower software with knowledge of audit trails and custom fields

Soft Skills:

  • Strong written and verbal communication

  • Ability to independently troubleshoot and resolve analytical issues

  • Sound knowledge of GLP regulations and audit readiness

Preferred Qualifications

  • Familiarity with Laboratory Management Systems (LMS), Electronic Lab Notebook (ELN), ERP, and QR coding

  • Experience with Mass Spectrometry (MS)

  • Knowledge of compendial standards (USP, FCC, NF) and monograph procedures

  • Exposure to ISO/IEC 17025 and prior work in QC/Analytical R&D or CRO environment is a plus

Apply now to become part of a global mission to strengthen the quality of medicines and help build a healthier world.

Employment Type: Full-time
Job Location: Hyderabad, India
Last Date to Apply: 5th May 2025
Experience Required: 3–6 years
Qualification: M.Pharm / M.Sc (Analytical/Organic/Pharmaceutical Analysis)

USP is proud to be an equal opportunity employer and is committed to diversity and inclusion in the workplace.

To apply for this job please visit usp.jobs.