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Senior Scientist I - Nmr

Usp
USP
7-11 years
Not Disclosed
Hyderabad
10 May 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Senior Scientist I – NMR


Organization Overview

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that develops globally recognized quality standards for medicines, dietary supplements, and food ingredients. USP collaborates with global scientific experts to strengthen public health systems through trusted standards.

USP promotes scientific excellence, integrity, and inclusive collaboration. With a presence in 20+ global locations and 1,300+ professionals, USP is committed to ensuring equitable participation in scientific advancement and improving global access to high-quality medicines.


Job Summary

The Senior Scientist I – NMR is a non-supervisory, laboratory-based scientific role within USP-India’s NMR Laboratory. The position involves advanced analytical work including NMR-based characterization, method development, validation, and reference standard evaluation.

The role supports development of scientific standards, regulatory compliance activities, and research initiatives while ensuring adherence to GLP/GMP and ISO guidelines. The candidate will also contribute to cross-functional scientific programs and laboratory quality systems.


Key Responsibilities

1. NMR Method Development & Analysis (70%)

  • Perform quantitative NMR (qNMR) method development and validation for reference standard development

  • Conduct structural elucidation and confirmation of chemical compounds using NMR techniques

  • Review and interpret NMR sample analysis reports as per monographs and internal procedures

  • Monitor reaction progress and perform analytical evaluations of compounds

  • Prepare detailed scientific reports and documentation

  • Coordinate with procurement and internal teams for project execution requirements


2. Laboratory Operations & Instrumentation (10%)

  • Ensure calibration and maintenance of laboratory instruments as per schedule

  • Execute IQ/OQ/PQ validation of new analytical instruments

  • Manage laboratory materials including glassware and chemicals

  • Maintain GLP-compliant laboratory environment and safety procedures

  • Support additional laboratory projects as required


3. Quality Systems, Compliance & Safety (10%)

  • Support development and implementation of laboratory safety initiatives

  • Participate in cross-functional scientific and quality teams

  • Develop and update SOPs and laboratory policies

  • Coordinate with Quality Assurance for corrective actions

  • Participate in internal audits including ISO 9001 and ISO 17025 compliance


4. Organizational Contribution (10%)

  • Promote Diversity, Equity, Inclusion, and Belonging (DEIB) initiatives within USP

  • Collaborate with global and internal teams to support scientific objectives

  • Contribute to continuous improvement initiatives within the laboratory


Required Qualifications

  • MSc in Analytical Chemistry / Organic Chemistry / M.Pharm with 10–13 years of experience in NMR
    OR

  • PhD in Chemistry or related field with 7–10 years of relevant experience


Required Skills & Expertise

  • Hands-on experience with NMR instrumentation

  • Strong expertise in small molecule structure elucidation

  • Experience working in GLP/GMP environments with proper documentation practices

  • Proficiency in Bruker NMR systems, including automation and cryo-probe technology

  • Knowledge of solid-state and multinuclear NMR techniques

  • Strong understanding of organic and analytical chemistry principles

  • Experience with electronic laboratory notebooks (ELN) preferred

  • Familiarity with ISO 17025 and GMP guidelines

  • Strong technical writing and communication skills

  • Ability to analyze and troubleshoot complex scientific problems


Preferred Skills

  • Experience with biological molecules (peptides, proteins, vaccines)

  • Exposure to platforms such as Empower, NuGenesis, and general pharmacopeial standards

  • Experience in reference standard development or pharmacopeial environments

  • Strong multi-tasking and prioritization skills in a regulated lab environment


Work Environment

  • On-site laboratory-based role

  • Exposure to regulated scientific and quality-controlled environments

  • Collaboration with internal scientific and global stakeholder teams


Supervisory Responsibilities

  • None (Individual Contributor Role)


Why Join USP

  • Work on globally impactful scientific standards that improve public health

  • Exposure to advanced analytical science and regulatory frameworks

  • Strong focus on scientific integrity, quality, and innovation

  • Inclusive and collaborative global scientific environment

  • Opportunities for continuous learning and professional development