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The United States Pharmacopeia (USP) is inviting applications for the position of Technical Associate in its Compendial Development Laboratory (CDL) based in Hyderabad. This is an excellent opportunity for entry-level professionals to join a globally recognized scientific organization dedicated to advancing public health and setting standards for medicine quality.
The role focuses on supporting USP’s core business through monograph modernization and the development of high-quality analytical standards.
Role Overview & Responsibilities
The Technical Associate is a non-supervisory role responsible for the execution of laboratory projects under the Global Laboratory Operations umbrella.
- Method Development & Validation: Perform analytical method development and validations for USP/NF monographs, specifically targeting Small Molecule projects.
- Monograph Modernization: Support the initiative to update and modernize existing monographs according to current scientific advancements.
- Compliance & Safety: Maintain a strict GLP (Good Laboratory Practice) environment and adhere to all safety protocols within the laboratory.
- Data Management: Prepare detailed project plans, validation reports, and maintain laboratory notebooks/Laboratory Management Systems (LMS) with high accuracy and data integrity.
- Standard Adherence: Execute projects in alignment with USP general chapters, standard operating procedures (SOPs), and international guidelines.
Candidate Profile
USP is looking for high-potential graduates who are passionate about analytical chemistry and pharmaceutical standards.
- Education: Master’s Degree (M.Sc) in Chemistry.
- Experience: 0–1 year (Freshers with strong academic backgrounds are encouraged to apply).
- Technical Knowledge: * Foundational understanding of USP/NF monographs, general chapters, and general notices.
- Ability to perform analytical validations for both Drug Substances and Drug Products.
- Awareness of ISO/IEC 17025 and QMS documentation procedures is highly desirable.
- Soft Skills: Strong technical writing skills, diplomatic communication, and a commitment to Diversity, Equity, Inclusion, and Belonging (DEIB).
Job Details
- Location: Hyderabad, India.
- Industry: Pharmaceutical / Healthcare / Quality Standards.
- Functional Area: Compendial Development Laboratory (CDL).
- Application Deadline: January 10, 2026. (Note: The source document listed 2025, but given the post date, this reflects the standard recruitment cycle).
How to Apply
Candidates who meet the eligibility criteria should apply through the USP Careers portal. This role offers a unique platform to work at the intersection of regulatory science and laboratory research, contributing to the global standards that ensure medicine safety.
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