Lupin is hiring for the position of Research Associate – IRF Analytical at its Pune, Maharashtra location. Candidates with 0–5 years of work experience and a Master’s degree in Pharmacy or Analytical Chemistry can apply.
The role involves analytical method development, drug product analysis, dissolution studies, laboratory documentation, and compliance with GLP and GDP requirements.
Job Details
| Particulars | Details |
|---|---|
| Company | Lupin |
| Job Role | Research Associate – IRF Analytical |
| Job Location | Pune, Maharashtra, India |
| Experience | 0–5 Years |
| Qualification | Master’s in Pharmacy or Analytical Chemistry |
| Job Date | 2 November 2026 |
Position
Research Associate – IRF Analytical
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Key Responsibilities
- Perform analytical method development for drug products, including assay, dissolution, degradation products, residual solvents, and water content.
- Use advanced analytical techniques such as HPLC, GC, UV, and KF.
- Maintain analytical documentation through the BIOVIA system, ensuring data integrity, traceability, version control, audit trail compliance, and secure electronic record management.
- Perform routine and initial analysis of drug products for market samples and query responses.
- Prepare method development protocols, reports, method equivalency reports, and Certificates of Analysis (COA).
- Conduct multimedia dissolution studies and compatibility studies and prepare corresponding reports.
- Maintain laboratory safety compliance during analysis.
- Ensure GLP (Good Laboratory Practice) compliance in the laboratory.
- Maintain GDP (Good Documentation Practice) standards in the laboratory.
Eligibility and Qualifications
Candidates must meet the following requirements:
- Master’s degree in Pharmacy (M.Pharm) or Analytical Chemistry.
- 0–5 years of relevant work experience.
Required Technical Skills
Candidates should have knowledge or experience in:
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- HPLC (High-Performance Liquid Chromatography)
- GC (Gas Chromatography)
- UV Spectroscopy
- KF (Karl Fischer) analysis
- Analytical method development
- Assay and dissolution testing
- Degradation product analysis
- Residual solvent analysis
- Multimedia dissolution studies
- Compatibility studies
- BIOVIA documentation system
- GLP and GDP compliance
- Analytical documentation and COA preparation