Technical Associate / Scientist I, CDL

The U.S. Pharmacopeial Convention (USP), a globally recognized organization advancing public health through the development of quality standards for medicines, dietary supplements, and food ingredients, is inviting applications for the position of Technical Associate / Scientist I in its Compendial Development Laboratory (CDL) under the Global Laboratory Operations division.

This is a fantastic opportunity for both fresh graduates and experienced professionals in the field of Chemistry or Pharmaceutical Sciences to contribute to a mission-driven organization that impacts health outcomes worldwide.

Technical Associate / Scientist I, CDL

Description

Brief Job Overview

This is a non-supervisory position in the Compendial Development Laboratory (CDL) within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP/NF monographs and maintaining safety and a GLP environment in the lab. This position is a component of USP’s core business, and the incumbent is expected to support monograph modernization initiatives.

How will YOU create impact here at USP?

In this role at USP, you contribute to USP’s public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.

The Technical associate/S-I has the following responsibilities:

• Engage in project planning, execution, method development, and validation of projects according to set standards such as USP general chapters, guidelines, SOPs, and protocols.
• Apply technical and scientific expertise in analytical method development and validation of pharmaceuticals.
• Prepare and review project plans, reports, laboratory notebooks/Laboratory Management System (LMS), and compile project data as required.
• Adhere to GLP and safety practices while working in the lab.
• Practice Diversity, Equity, Inclusion, and Belonging principles at USP India.

Who is USP Looking For?

The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

Experience for Technical associate:

• Master’s Degree in Chemistry (Analytical/ Organic) or Pharmaceutical Sciences with 0-1 years of experience in the relevant field.

Experience for S-I:

• Master’s Degree in Chemistry (Analytical/ Organic) or Pharmaceutical Sciences with 1-3 years of experience in the relevant field.

Skill set required:

• Possess a fine understanding of USP/NF monographs, general chapters, and general notices.
• Exposure to GMP/GLP/QMS environment and documentation procedures, and champions data integrity.
• Capable of performing analytical method development and validations using HPLC and GC techniques and protocols.
• Analytical skills in handling method development and validations for drug substances, drug products.
• Should have exposure to GMP/GLP environment and documentation procedures.
• Awareness of ISO/IEC 17025 is desirable.

Additional Desired Preferences

• Exceptional breadth of pharmaceutical industry experience.
• Excellent technical writing and oral communication skills required.
• Must be able to communicate effectively with diplomacy and enthusiasm.
• Technical and analytical skills required, including the ability to interpret technical information.
• Must have hands-on experience in working with chemical methods and handling instruments like UHPLC, FTIR, KF and UV-Visible.
• Should have a good understanding of GLP regulations and exposure to external regulatory audits.

Why Join USP?

At USP, you get to be part of a scientific community that impacts millions of lives by setting the standards that ensure the quality, purity, and consistency of medicines and healthcare products across the globe. The organization offers a collaborative culture, professional development, and a purpose-driven career path.

If you are looking to launch or elevate your career in pharmaceutical analysis and regulatory science, this is your chance to work with a prestigious name in global healthcare standards.

📢 Apply Now!
Visit the USP Careers Portal and search for Req ID: SCIEN002662

OR

APPLY HERE