Aizant Drug Research Solutions Pvt. Ltd., a leading integrated pharmaceutical and life sciences organization, has announced a Walk-In Interview for Quality Control professionals. This recruitment drive is aimed at candidates with 1–3 years of experience in analytical testing, stability studies, and raw material sampling. The opportunity is based at Aizant’s facility in Dulapally, Hyderabad.

Candidates with experience in HPLC, GC, UV Spectroscopy, Dissolution Testing, Stability Sample Management, and Raw Material Analysis are encouraged to attend the interview.

Interview Details

Details

Company

Aizant Drug Research Solutions Pvt. Ltd.

Department

Quality Control

Interview Date

19th June 2026

Time

9:00 AM Onwards

Experience

1–3 Years

Job Location

Dulapally, Hyderabad

Venue

Aizant Drug Research Solutions Pvt. Ltd. (Clinical Block), EMC Maithrivihar Complex, Ameerpet, Hyderabad

Open Positions

1. IPFP (In-Process Finished Product)

Experience Required: 1–3 Years

Technical Skills:

HPLC Analysis

UV Spectroscopy

Gas Chromatography (GC)

Dissolution Testing

Related Substances Analysis

GMP Documentation Practices

2. Stability

Experience Required: 1–3 Years

Technical Skills:

Dissolution Analysis

HPLC Testing

Stability Sample Management

Related Substances Testing

Stability Study Documentation

Data Integrity Compliance

3. Raw Materials

Experience Required: 1–3 Years

Technical Skills:

Sampling of Raw Materials

Packing Material Sampling

Material Identification

GMP Documentation

Warehouse Sampling Procedures

Quality Compliance Practices

Why Join Aizant?

Aizant is recognized for its strong presence in pharmaceutical research, development, manufacturing, and clinical services. Employees gain exposure to advanced analytical instruments, regulated environments, and international quality standards. The company offers opportunities to work with modern laboratories while building expertise in pharmaceutical quality systems.

Documents Required

Candidates attending the walk-in interview should carry:

Updated Resume/CV

Educational Certificates

Experience Letters

Latest Salary Slips

Government Photo ID Proof

Passport-Size Photographs

Candidates unable to attend the interview may share their resumes through the email address mentioned in the official notification.

Selection Process

The selection process may include:

Resume Screening

Technical Discussion

Analytical Skill Assessment

HR Interview

Final Selection and Offer Discussion

5 Technical Interview FAQs for Quality Control

1. What is the purpose of system suitability in HPLC?

Answer:

System suitability verifies that the HPLC system is performing correctly before sample analysis. Parameters such as theoretical plates, tailing factor, resolution, and %RSD are evaluated to ensure reliable analytical results.

2. What is the difference between assay and related substances testing?

Answer:

Assay determines the amount of active pharmaceutical ingredient (API) present in a sample, while related substances testing identifies and quantifies impurities, degradation products, and process-related contaminants.

3. Why is dissolution testing important in pharmaceuticals?

Answer:

Dissolution testing measures the rate and extent of drug release from a dosage form. It helps predict product performance, ensures batch consistency, and supports regulatory compliance.

4. What precautions should be followed during raw material sampling?

Answer:

Sampling should be performed in designated areas using clean tools and approved procedures. Proper labeling, contamination control, and representative sample collection are essential to maintain material integrity.

5. What is the significance of stability studies?

Answer:

Stability studies evaluate how a pharmaceutical product maintains its quality, safety, and efficacy over time under various environmental conditions. These studies help establish shelf life and storage requirements.

Conclusion

The Aizant Walk-In Interview 2026 presents an excellent opportunity for Quality Control professionals looking to advance their careers in the pharmaceutical industry. Candidates with hands-on experience in HPLC, GC, Dissolution, Stability Studies, and Raw Material Sampling should take advantage of this opportunity and attend the interview on 19th June 2026 in Hyderabad.