US Pharmacopeia (USP) Fresher Recruitment | Technical Associate/Scientist I

USP Hiring Technical Associate/Scientist I – Chemistry & Scientific Standards | Hyderabad

Join USP India as a Technical Associate/Scientist I – CDL

Are you passionate about the development and validation of analytical methods in pharmaceuticals? United States Pharmacopeia (USP) India seeks a Technical Associate/Scientist I in the Compendial Development Laboratory (CDL) within Global Laboratory Operations in Hyderabad. This is a full-time, non-supervisory role focused on supporting monograph modernization initiatives and maintaining a GLP environment in the lab.

Why Join USP?

At USP, you will contribute to improving global health through pharmaceutical quality standards. We invest in employee growth and development as part of our inclusive and diverse work environment, ensuring a productive and engaging workplace.

Job Role & Responsibilities

As a Technical Associate/Scientist I, your key responsibilities include:

• Engaging in project planning, execution, analytical method development, and validation according to USP general chapters, guidelines, SOPs, and protocols.
• Developing and validating pharmaceutical analytical methods using HPLC, GC, FTIR, KF, and UV-Visible spectrophotometry.
• Ensuring GLP, GMP, and QMS compliance in all lab activities.
• Preparing and reviewing project reports, laboratory notebooks, and documentation in the Laboratory Management System (LMS).
• Upholding data integrity and following ISO/IEC 17025 guidelines.
• Practising Diversity, Equity, Inclusion, and Belonging at USP India.

Who Can Apply?

USP is looking for professionals who meet the following criteria:

For Technical Associate:

• Education: Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences
• Experience: 0-1 year in analytical method development and validation

For Scientist I:

• Education: Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences
• Experience: 1-3 years in analytical method development and validation

Required Skills:

• Strong understanding of USP/NF monographs, general chapters, and notices.
• Experience in HPLC, GC, FTIR, KF, and UV-visible spectrophotometry.
• Exposure to GMP, GLP, and QMS environments.
• Proficiency in technical writing, documentation, and data analysis.
• Awareness of ISO/IEC 17025 standards.

Preferred Skills:

• Experience in the pharmaceutical industry.
• Strong communication and analytical skills.
• Hands-on experience with advanced analytical instruments.
• Prior exposure to external regulatory audits.

Work Location: Hyderabad, India

Benefits of Working at USP

USP offers a comprehensive benefits package, including:

• Competitive salary and performance-based incentives.
• Comprehensive healthcare options for employees and their families.
• Paid time off and flexible work arrangements.
• Retirement savings plans.
• Opportunities for professional development and career growth.

How to Apply?

Interested candidates can apply online through the official USP careers page. Don’t miss this opportunity to be part of an organization committed to global health and pharmaceutical quality!

🔗 Apply Now: USP Careers – Technical Associate/Scientist I

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