The U.S. Pharmacopeial Convention (USP), a globally recognized scientific organization, is seeking a Scientist IV / Scientist III for its Compendial Development Laboratory (CDL) in Hyderabad, India. This is an exciting opportunity for professionals with a Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences and significant experience in analytical method development and validation. If you are passionate about ensuring the quality and safety of medicines and supplements, this role is for you.
About USP:
USP is an independent scientific organization that collaborates with global health and science authorities to develop quality standards for medicines, dietary supplements, and food ingredients. With over 1,300 professionals across 20 global locations, USP is committed to strengthening the supply of safe, quality medicines worldwide.
Job Title: Scientist IV / Scientist III – Compendial Development Laboratory
Location: Hyderabad, India
Industry Type: Pharma/Healthcare/Clinical Research
Functional Area: Compendial Development Laboratory
Qualification: Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences
Experience: 5+ years
End Date: 30th March 2025
Job Description:
Brief Job Overview:
This is a non-supervisory role within USP’s Global Laboratory Operations. The selected candidate will be responsible for analytical method development and validation for USP/NF monographs, ensuring compliance with GLP (Good Laboratory Practices) and maintaining a safe laboratory environment. The role also supports USP’s monograph modernization initiatives, a core component of its business.
Key Responsibilities:
- Plan and execute projects, including method development and validation, adhering to USP general chapters, guidelines, SOPs, and protocols.
- Utilize technical expertise in HPLC, GC, UHPLC, LC-MS, GC-MS, FTIR, KF, and UV-Visible techniques for pharmaceutical analysis.
- Prepare and review project plans, reports, and laboratory documentation while ensuring data integrity.
- Maintain compliance with GLP, GMP, and QMS standards.
- Promote Diversity, Equity, Inclusion, and Belonging (DEIB) principles within the workplace.
Candidate Profile:
Experience Requirements:
- Scientist III:
- Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 6-8 years of experience, or
- Ph.D. with 1-3 years of experience in the relevant field.
- Scientist IV:
- Master’s Degree in Chemistry (Analytical/Organic) or Pharmaceutical Sciences with 8-10 years of experience, or
- Ph.D. with 4-7 years of experience in the relevant field.
Technical Skills:
- Strong understanding of USP/NF monographs, general chapters, and general notices.
- Hands-on experience with analytical instruments such as HPLC, GC, GPC-RI, SEC-MALS, and more.
- Proficiency in method development and validation for drug substances, drug products, and polymers.
- Familiarity with GMP/GLP environments and documentation procedures.
- Knowledge of ISO/IEC 17025 standards is desirable.
Additional Preferences:
- Exceptional pharmaceutical industry experience.
- Excellent technical writing and oral communication skills.
- Ability to interpret technical information and communicate effectively.
- Exposure to external regulatory audits is a plus.
Why Join USP?
- Be part of a global mission to ensure the quality and safety of medicines and supplements.
- Work in a collaborative and inclusive environment that values Equity, Excellence, and Passion for Quality.
- Gain exposure to cutting-edge analytical techniques and regulatory standards.
