Are you an analytical chemistry professional with a passion for advancing public health? USP is looking for a Scientist II to join the Reference Standard Laboratory (RSL) in Hyderabad, India. This full-time role offers an exciting opportunity to contribute to global health initiatives while honing your expertise in pharmaceutical analysis. Here’s everything you need to know about this position, from company background to the application process.
Company Introduction: About USP
The United States Pharmacopeia (USP) is a leading organization dedicated to improving global health through public standards and programs. By ensuring equitable access to high-quality, safe medicines, USP plays a vital role in advancing public health worldwide. The organization values inclusive management styles and invests in employee development to foster a productive and engaging work environment.
Responsibilities in the Scientist II Role
As a Scientist II in the Reference Standard Laboratory, you will:
- Conduct high-precision testing and data analysis with minimal errors.
- Support various departmental teams, including Verification, GPH, PQM, and stability teams.
- Manage sample archival, tracking, and chemical inventory.
- Perform instrument calibration and execute IQ/OQ/PQ for new equipment.
- Troubleshoot and resolve scientific challenges in projects as needed.
- Ensure compliance with GLP (Good Laboratory Practices) and safety protocols.
- Actively participate in internal and external audits and certifications.
Your work will directly impact USP’s mission to ensure access to high-quality medicines globally.
Qualifications and Skills
Educational Requirements
- A Master’s degree in Chemistry or Pharmacy.
Experience
- 3 to 6 years of laboratory experience, particularly in pharmaceutical testing.
- Expertise in chromatographic techniques such as HPLC.
Key Skills
- Proficiency in analytical instrumentation like HPLC, GC, spectroscopic techniques, and wet analytical methods.
- Knowledge of pharmaceutical testing protocols (USP compendia, ICH guidelines, FDA regulations).
- Hands-on experience with Empower software, including audit trails and custom fields.
- Strong understanding of GLP regulations and exposure to regulatory audits.
- Effective communication and interpersonal skills.
Preferred Skills
- Familiarity with advanced analytical instruments (GC, Mass analyzers, Thermal analysis).
- Experience with ERP systems, Electronic Laboratory Notebooks, and QR coding systems.
- Awareness of ISO/IEC 17025 standards and prior exposure to high-volume QC or contract labs.
