The United States Pharmacopeial Convention (USP) is a scientific nonprofit organization that establishes public standards for the quality of medicines and their ingredients. With a commitment to improving global health, USP’s mission is to ensure that everyone has access to safe, high-quality medicines. Our operations are geared toward supporting the healthcare community through rigorous science and standards that enhance public health.
Job Description:
USP is seeking a highly motivated Technical Associate / Scientist I to join our Compendial Development Laboratory (CDL) in Hyderabad. This is a non-supervisory full-time position focused on analytical method development, validation, and contributing to the modernization of monographs. The successful candidate will work to ensure compliance with Good Laboratory Practices (GLP) and uphold the highest standards of laboratory safety.
Key Responsibilities:
- Engage in project planning, execution, and method development in alignment with USP standards, guidelines, SOPs, and protocols.
- Apply technical expertise in the analytical method development and validation of pharmaceutical materials.
- Prepare and review project plans, laboratory notebooks, and compile necessary project data.
- Adhere to GLP and safety practices while working collaboratively in the laboratory environment.
- Promote diversity, equity, inclusion, and belonging principles within the USP India team.
Qualifications:
- For Technical Associate: Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 0-1 years of relevant experience.
- For Scientist I: Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 1-3 years of relevant experience.
Skills Required:
- Solid understanding of USP/NF monographs, general chapters, and notices.
- Experience in a GMP/GLP/QMS setting and familiarity with documentation procedures.
- Proficient in analytical method development and validation techniques using HPLC and GC.
- Hands-on experience with laboratory instruments, such as UHPLC, FTIR, KF, and UV-Visible spectrophotometers.
- Strong analytical skills and an understanding of GLP regulations, as well as exposure to external regulatory audits.
Additional Preferences:
- Broad experience within the pharmaceutical industry.
- Excellent technical writing and oral communication skills.
- Ability to effectively communicate with enthusiasm and diplomacy.
Benefits:
USP offers a comprehensive benefits package to support the well-being of employees and their families, including paid time off, healthcare options, and retirement savings plans.
How to Apply:
