Lupin is recruiting for the position of Research Associate – IRF Analytical at its Pune, Maharashtra location. The role focuses on analytical method development, method validation and transfer, Good Laboratory Practice (GLP) documentation, and analytical support for regulatory queries and quality control investigations.
Candidates with a master’s degree in Analytical Chemistry or Pharmacy and 0–5 years of work experience can apply.
Job Details
| Particulars | Details |
|---|---|
| Company | Lupin |
| Job Title | Research Associate – IRF Analytical |
| Job Location | Pune, Maharashtra, India |
| Experience | 0–5 years |
| Qualification | Master’s in Analytical Chemistry or Pharmacy |
| Date Listed | October 27, 2026 |
Position: Research Associate – IRF Analytical
The Research Associate will work on analytical method development and validation for drug products, prepare analytical specifications and test procedures, maintain GLP documentation, and support regulatory queries and site quality control investigations.
Key Responsibilities
- Develop analytical methods for assay, related substances, and dissolution using chromatographic methods.
- Perform analytical method validation and method transfer.
- Prepare specifications, standard test procedures, and method development reports for drug products and excipients.
- Maintain and update GLP documentation.
- Maintain a Good Laboratory Practice (GLP) environment.
- Provide timely support in resolving regulatory queries.
- Assist with site Quality Control (QC) investigations.
Eligibility and Qualifications
- Educational Qualification: Master’s degree in Analytical Chemistry or Pharmacy.
- Experience: 0–5 years.
Required Skills and Knowledge
Based on the listed job responsibilities, relevant knowledge areas include:
- Analytical method development.
- Chromatographic methods for assay, related substances, and dissolution.
- Analytical method validation and transfer.
- Preparation of analytical specifications and standard test procedures.
- GLP documentation and laboratory practices.
- Regulatory query support and QC investigations.
