Gowrie Research Pvt. Ltd. has announced a Walk-In Interview drive for experienced pharmaceutical professionals in the Analytical Development Laboratory (ADL) department. The recruitment drive will be conducted from 24th August to 26th August 2026 between 11:00 AM and 7:00 PM at Vadodara, Gujarat. Candidates with experience in formulation analytical development and expertise in oral solid dosage or liquid oral products are encouraged to attend.

Company Overview

Gowrie Research Pvt. Ltd. is a pharmaceutical research organization engaged in formulation research and development, analytical method development, product characterization, stability studies, and regulatory support activities. The company focuses on developing high-quality pharmaceutical formulations while maintaining compliance with global regulatory standards.

Walk-In Interview Details

Interview Dates: 24th August 2026 to 26th August 2026

Interview Time: 11:00 AM to 7:00 PM

Walk-In Venue:

B&S House, Ground & 1st Floor, N.H. No. 8,

Opposite GSFC University, Dashrath,

Vadodara, Gujarat – 391740

Department

Analytical Development Laboratory (ADL)

Candidates having experience in Liquid Oral and Solid Oral formulations will be given preference.

Available Positions

1. Research Associate – ADL

Number of Positions: 4

Experience Required: 2 to 4 Years

Qualification: M.Sc., B.Pharm, or M.Pharm

2. Assistant Manager – ADL

Number of Positions: 1

Experience Required: 8 to 10 Years

Qualification: M.Sc., B.Pharm, or M.Pharm

Educational Qualification

Candidates should possess any of the following qualifications:

Master of Science (M.Sc.)

Bachelor of Pharmacy (B.Pharm)

Master of Pharmacy (M.Pharm)

Preferred Experience

Applicants should have hands-on experience in:

Analytical method development and validation

HPLC and UV analytical techniques

Stability studies and data interpretation

Dissolution method development

Regulatory documentation

Analytical troubleshooting

Raw material and finished product analysis

Oral solid dosage formulation analysis

Liquid oral product characterization

Key Responsibilities

Research Associate

Perform analytical testing of formulation samples.

Execute method development and validation activities.

Conduct stability studies as per ICH guidelines.

Prepare analytical reports and documentation.

Support formulation development projects.

Operate and maintain analytical instruments.

Assistant Manager

Lead analytical development projects.

Review analytical data and reports.

Manage laboratory compliance activities.

Coordinate with formulation and regulatory teams.

Guide junior analysts and researchers.

Ensure adherence to quality and regulatory requirements.

Required Technical Skills

HPLC Operation and Troubleshooting

UV Spectrophotometry

Dissolution Testing

Method Validation

Stability Study Evaluation

Data Integrity Compliance

Regulatory Documentation

Good Laboratory Practices (GLP)

Analytical Method Transfer

Root Cause Investigation

Why Join Gowrie Research?

Opportunity to work in advanced formulation R&D projects.

Exposure to analytical development and regulatory activities.

Career growth in the pharmaceutical research sector.

Collaborative research environment.

Learning opportunities with experienced professionals.

Documents to Carry

Candidates attending the interview should carry:

Updated Resume/CV

Educational Certificates

Experience Certificates

Latest Salary Slip

Government Photo ID Proof

Passport Size Photographs

Technical FAQs

1. What is Analytical Development Laboratory (ADL) in the pharmaceutical industry?

ADL is responsible for developing, validating, and transferring analytical methods used to evaluate pharmaceutical products, raw materials, and stability samples to ensure quality and regulatory compliance.

2. Why is HPLC important in analytical development?

High-Performance Liquid Chromatography (HPLC) is widely used for assay determination, impurity profiling, degradation studies, and method validation, making it one of the most critical analytical tools in pharmaceutical R&D.

3. What is analytical method validation?

Analytical method validation is the process of demonstrating that an analytical procedure is suitable for its intended purpose by evaluating parameters such as accuracy, precision, specificity, linearity, robustness, and detection limits.

4. What are stability studies in pharmaceutical development?

Stability studies assess how a pharmaceutical product maintains its quality, safety, and efficacy under various environmental conditions such as temperature and humidity throughout its shelf life.

5. What is dissolution testing and why is it important?

Dissolution testing measures the rate and extent of drug release from a dosage form. It is essential for formulation development, bioequivalence assessment, quality control, and regulatory approval.

Conclusion

The Gowrie Research Pvt. Ltd. Walk-In Interview 2026 offers an excellent opportunity for experienced professionals in Analytical Development to build a rewarding career in pharmaceutical research and development. Candidates with expertise in oral solid and liquid oral formulations, analytical method development, and laboratory operations are encouraged to participate in this recruitment drive and explore growth opportunities within the organization.