Position Details
About this role
This role supports stewardship, curation, and integration of chemical, biologic, and vaccine product reference data across the drug development lifecycle. You will derive and validate nomenclature, curate master/reference data, standardize structures, and uphold data governance and regulatory compliance.
Key Responsibilities
- Derive and assign correct chemical nomenclature (IUPAC and CAS style) for small molecules and related entities
- Create, maintain, and curate company reference/master data with metadata across the lifecycle
- Enter, proofread, validate, and review data integrity in centralized systems
- Apply structure standardization and substance representation (SMILES, InChI, Mol files) and support normalization
- Ensure compliance with regulatory and industry standards (GxP, 21 CFR part 11, ICH, IDMP, WHO Drug Dictionary)
Technical Overview
The work focuses on chemical nomenclature and regulated master/reference data management, including validation/proofreading, structure normalization (SMILES, InChI, Mol files), and applying canonical data models and metadata definitions. It also includes participating in SDLC and end-user acceptance testing for reference data systems, with opportunities to evaluate ML/NLP for curation assistance.
Ideal Candidate
The ideal candidate is a senior scientific data specialist with deep organic chemistry experience and strong capability deriving and validating chemical nomenclature (IUPAC and CAS-style). They have extensive hands-on experience curating reference/master data, enforcing data quality rules, and standardizing molecular representations using SMILES, InChI, and Mol files in regulated environments (GxP, 21 CFR part 11, ICH/IDMP).
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Must have completed at least one year of organic chemistry
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