U.S. Pharmacopeial Convention looking for RSL Scientist - M.Pharm, MSc Apply

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.

Post : Scientist II, RSL (Stability)

Brief Job Overview
This is a key hands-on, non-supervisory position. In this role, the Scientist initiates and executes stability studies for reference standards using appropriate compendial methods. Additionally, the incumbent will be responsible for performing analytical method development and validations for Impurity RS and maintaining safety and GLP environment in the lab. The Scientist will contribute to the scientific expertise and work ethic of the laboratory through a broad range of technical support and knowledge. The scientist has mastered many common techniques in the laboratory and can contribute their own observations and input to difficult projects. The incumbent will provide technical assistance to the Stability Program by performing analytical tests, reviewing analytical data, and preparing summary reports. The incumbent may execute 90% - 100% of their work at the bench level.

• Conducts stability testing and records data.
• Prepares reports, evaluates trends, and develops models.
• Executes testing with minimal errors.
• Completes projects on time and responds to QA.
• Experienced in method development and validation using HPLC and GC.
• Designs and executes experiments and validations.
• Prepares protocols and engages in project planning.
• Improves lab operations and aligns projects with goals.
• Prepares SOPs, ensures GLP, and calibrates equipment.
• Solves complex problems with scientific approach.
• Follows USP standards and prepares for ISO certifications.
• Supports collaborative testing and other teams.
• Committed to continuous learning.

Candidate Profile
• Education : Master's in M.Sc. (analytical/organic) or M. Pharma (pharmaceutical sciences/analysis).
• Experience : 3-6 years relevant experience in pharmaceutical analytical laboratory.
• Skills :
• Pharmaceutical testing for APIs and Formulations.
• Chromatographic systems (HPLC, GC) handling and troubleshooting.
• Expert in Empower software with knowledge on Audit trails and Custom fields.
• Wet chemical analysis (Titrations, IR, KF, UV, Thermal, Elemental analysis).
• Stability chambers management and monitoring.
• Long-term and shipping stability studies per USP internal guidelines and WHO, ICH guidelines.
• Analytical method development and validation.
• Lab management systems and electronic laboratory notebooks.
• Attributes : Excellent communication, highly responsible, adaptable, and capable of leading change.

Additional Desired Preferences
• Having knowledge of Lab Management System (LMS) and Electronic Laboratory Notebook, ERP, QR coding system is an added advantage.
• Hands-on experience in handling instruments like MS is an added advantage.
• Understanding monograph procedures and participating in compendial methods for reference materials (USP, FCC, NF, etc.).
• Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D, or a contract pharmaceutical analytical laboratory testing organization is a plus.
• Awareness of ISO/IEC 17025 is desirable.

Additional Information
Experience : 3-6 years
Qualification : Master's in M.Sc. (analytical/organic) or M.Pharma
Location : Hyderabad, IND
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : RSL (Stability)
End Date : 20th May 2025