JAMP India Pharmaceuticals Pvt. Ltd., a part of the JAMP Pharma Group, is conducting a Walk-In Interview Drive on 14th June 2026 (Sunday) for experienced professionals in Formulation Development and Analytical Development. This recruitment initiative is aimed at candidates with expertise in developing pharmaceutical formulations across OSD, Semisolids, Ophthalmic, Oral Liquids, and Nasal dosage forms.
This is an excellent opportunity for talented pharmaceutical professionals looking to advance their careers in a reputed R&D environment focused on innovation, product development, and regulatory excellence.
Job Overview
Particulars Details
Company
JAMP India Pharmaceuticals Pvt. Ltd.
Department
Formulation Development & Analytical Development
Qualification
M.Sc / M.Pharm
Experience
3–6 Years
Designation Level
Executive
Number of Positions
25
Location
Hyderabad
Interview Date
14th June 2026 (Sunday)
Interview Time
10:00 AM – 02:30 PM
Key Skills Required
Candidates should possess hands-on experience in:
Formulation Development for OSD, Semisolids, Ophthalmic, Oral Liquids, and Nasal products
Analytical method development and validation
LCMS/MS and GCMS/MS techniques
IVRT (In Vitro Release Testing)
Q3 characterization studies
Stability studies and regulatory documentation
Pharmaceutical R&D processes and troubleshooting
Walk-In Venue
JAMP India Pharmaceutical Pvt. Ltd. (R&D Center)
Plot No. 40 & 41 (Part), Phase 3, Biotech Park,
Karkapatla Village, Hyderabad, Telangana, India.
Date: 14th June 2026 (Sunday)
Time: 10:00 AM to 02:30 PM
Why Join JAMP India?
JAMP India Pharmaceuticals provides professionals with an opportunity to work on advanced pharmaceutical development projects and global product portfolios. Employees gain exposure to innovative technologies, regulatory requirements, analytical techniques, and cross-functional collaboration within a research-driven environment.
The company emphasizes scientific excellence, continuous learning, and career growth, making it an attractive destination for experienced pharmaceutical professionals.
Technical FAQs
1. What is the role of LCMS/MS in pharmaceutical analytical development?
LCMS/MS (Liquid Chromatography-Mass Spectrometry/Mass Spectrometry) is used for impurity profiling, bioanalysis, trace-level quantification, degradation studies, and method development. It provides high sensitivity and specificity for complex pharmaceutical samples.
2. Why are stability studies important during formulation development?
Stability studies evaluate how a drug product maintains its quality, safety, and efficacy over time under different environmental conditions. These studies help establish shelf life, storage conditions, and packaging requirements.
3. What is IVRT and why is it used for semisolid formulations?
In Vitro Release Testing (IVRT) measures the rate and extent of drug release from semisolid dosage forms such as creams, gels, and ointments. It is essential for formulation optimization, quality control, and regulatory submissions.
4. What are Q3 characterization studies in pharmaceutical development?
Q3 studies focus on the physical and structural characterization of drug products, including particle size distribution, rheology, viscosity, morphology, and microstructure. These studies are particularly important for demonstrating equivalence in complex generic products.
5. What is the difference between method development and method validation?
Method development involves creating an analytical procedure suitable for testing a product, while method validation confirms that the developed method consistently produces accurate, precise, specific, and reliable results according to regulatory guidelines such as ICH Q2.
Final Thoughts
The JAMP India Pharmaceuticals Walk-In Interview 2026 presents a valuable opportunity for experienced M.Sc and M.Pharm professionals seeking careers in Formulation Development and Analytical Development. Candidates with expertise in advanced analytical techniques, stability studies, and pharmaceutical product development are encouraged to attend the interview and explore growth opportunities within a globally connected pharmaceutical organization.


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