USP Pharmaceutical Sciences Chemistry Scientist Job – Apply Online
Scientist I, CDL
Location: Hyderabad, IND
Job Category: Chemistry & Scientific Standards
Job Type: Full-Time
Req ID: SCIEN002525
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 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. 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, including training in inclusive management styles and other competencies necessary for ensuring engaged and productive work environments.
The Scientist I has the following responsibilities:
- Engage in project planning, execution, method development, and validation of projects according to USP general chapters, guidelines, SOPs, and protocols.
- Apply technical and scientific expertise in analytical method development and validation of Small molecule projects.
- Prepare 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, a commitment to excellence through inclusive and equitable behaviors and practices, and the ability to quickly build credibility with stakeholders, along with the following competencies and experience:
- Master’s degree in Chemistry with 1-3 years of experience
- Fine understanding of USP/NF monographs, general chapters, and general notices
- Exposure to GMP/GLP/QMS environment and documentation procedures, championing data integrity
- Capability in performing analytical method developments and validations using modern techniques and protocols
- Strong analytical skills in handling method developments and validations for drug substances and drug products
- Awareness of ISO/IEC 17025 is desirable
Additional Desired Preferences
The following preferences highlight any additional expertise to perform the role effectively. Note that these items are not requirements nor disqualify candidates for consideration:
- Master’s degree in Chemistry or Pharmaceutical Sciences with 1-3 years of experience in a relevant field
- Hands-on experience with chemical methods and instruments like HPLC, GC, IC, ICP-OES/MS, FT-IR, UV-Visible, AAS, and KF
- Fair understanding of GLP regulations and exposure to external regulatory audits
- Technical knowledge in the areas of drug substances, drug products, and various dosage forms
- Strong technical and analytical skills, with the ability to interpret technical information
- Broad experience in the Pharma industry
- Excellent technical writing and oral communication skills
- Effective communication abilities with diplomacy and enthusiasm
Click here to apply for the position of Scientist I at USP
Keywords: Scientist I, CDL, Hyderabad, Chemistry, Scientific Standards, Full-Time, USP, Public Health, Global Health. USP Pharmaceutical Sciences Chemistry Scientist Job – Apply Online. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.
