Job Title
Senior Scientist I – NMR Laboratory
Work Mode
Onsite / Laboratory-Based
Work Type
Non-Supervisory Role
Organization
United States Pharmacopeia (USP) (USP–India)
About USP
United States Pharmacopeia (USP) is a global scientific organization dedicated to developing trusted public standards that ensure the quality, safety, and efficacy of medicines worldwide. USP fosters inclusive scientific collaboration and evidence-based decision-making to strengthen global public health systems. The organization emphasizes scientific integrity, regulatory excellence, and equitable participation in scientific advancement.
Job Summary
We are seeking an experienced Senior Scientist I – NMR Laboratory to contribute to advanced analytical research and molecular characterization activities.
The role focuses on Nuclear Magnetic Resonance (NMR)-based structure elucidation, quantitative NMR (qNMR) method development and validation, reference standard development, and analytical support for synthetic chemistry and biologics-related projects. The position also supports GLP compliance, laboratory safety, and quality systems in alignment with global regulatory standards.
Key Responsibilities
NMR Analysis & Method Development (70%)
Perform quantitative NMR (qNMR) method development and validation for development of reference standards.
Conduct structure confirmation and molecular characterization using NMR techniques.
Support development of reference materials and certified standards.
Review NMR analytical reports for compliance with monographs and internal procedures.
Perform reaction monitoring and interpret NMR data for synthetic chemistry applications.
Prepare and review scientific reports and documentation for project deliverables.
Coordinate with procurement and internal teams to ensure timely project execution.
Instrument Calibration & Laboratory Operations (10%)
Ensure timely calibration and maintenance of laboratory instruments.
Execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for new instruments.
Manage procurement of laboratory consumables including glassware and chemicals.
Maintain GLP-compliant and safe laboratory environment.
Support additional scientific or operational projects as required.
Quality Systems, Safety & Compliance (10%)
Support laboratory safety initiatives and implement safety best practices.
Develop and maintain Standard Operating Procedures (SOPs) for NMR laboratory operations.
Coordinate with Quality Assurance teams for corrective and preventive actions (CAPA).
Participate in internal, ISO 9001, and ISO 17025 audits.
Ensure compliance with GMP, GLP, and regulatory guidelines.
Scientific Collaboration & DEI Contribution (10%)
Participate in cross-functional scientific teams and collaborative research projects.
Promote Diversity, Equity, Inclusion, and Belonging (DEI&B) principles within USP.
Contribute to building an inclusive, collaborative, and high-performance work environment.
Required Qualifications
MSc in Analytical Chemistry / Organic Chemistry / M.Pharm with 10–13 years of experience in NMR
OR
PhD in relevant discipline with 7–10 years of NMR experience
Required Skills & Expertise
Technical Expertise
Hands-on experience with NMR instrumentation.
Strong knowledge of small molecule structure elucidation using NMR.
Experience with Bruker NMR systems, automation software, and cryo-probes.
Knowledge of solid-state NMR and multinuclear NMR techniques.
Understanding of synthetic organic chemistry and analytical chemistry principles.
Regulatory & Quality Systems
Experience working in GMP / GLP environments.
Knowledge of ISO 17025 and ISO 9001 standards.
Experience with documentation and electronic lab notebooks (ELN preferred).
Data & Scientific Skills
Strong ability to analyze and interpret complex NMR data.
Experience in troubleshooting technical and analytical challenges.
Strong scientific writing and documentation skills.
Soft Skills
Strong communication and interpersonal skills.
Ability to collaborate with internal and external stakeholders.
Strong problem-solving and decision-making ability.
Ability to manage multiple priorities and deliver high-quality results on time.
Self-driven with strong ownership and accountability.
Preferred Skills (Added Advantage)
Experience with biologics (peptides, proteins, vaccines).
Knowledge of platforms such as Empower, NuGenesis, and ELN systems.
Experience in general chapter development and reference standards.
Working Environment
Laboratory-based role with exposure to chemical and analytical environments.
Adherence to strict safety, GLP, and regulatory compliance standards.
Collaborative scientific environment with global stakeholders.
Why Join USP
Contribute to global public health through development of trusted scientific standards.
Work in a highly research-driven and regulated scientific environment.
Engage in advanced NMR research and reference standard development.
Be part of an inclusive organization focused on scientific excellence and equity.
Opportunity to impact global medicine quality and healthcare systems.
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