Ajanta Pharma Limited, a leading specialty pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality finished dosage formulations for domestic and international markets, has announced a Walk-In Interview Drive for its formulation manufacturing facility at Guwahati, Assam.

The company is inviting qualified and experienced pharmaceutical professionals from Quality Control, Oral Solid Dosage (OSD), and Liquid Dosage Manufacturing & Packing departments to participate in the recruitment drive.

Walk-In Interview Details

Interview Date: 14 June 2026 (Sunday)

Time: 09:00 AM to 05:00 PM

Venue: Sunder Resort, Majithar, Sikkim

Candidates unable to attend the walk-in interview may send their updated resumes to the company’s recruitment email.

Departments Hiring

1. Quality Control (QC)

Position: Officer / Senior Officer

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

Experience: 2–8 Years

Key Responsibilities

Analysis of raw materials, packaging materials, water samples, in-process and finished products

Operation and calibration of analytical instruments such as HPLC, GC, and Autotitrator

Stability sample analysis and documentation

Preparation and standardization of volumetric solutions and reagents

Handling of reference standards and working standards

Knowledge of OOS, OOT, LIMS, QMS, and laboratory investigations

2. Oral Solid Dosage (OSD) – Manufacturing

Position: Officer / Senior Officer

Qualification: B.Pharm

Experience: 3–7 Years

Key Responsibilities

Granulation, Compression, Coating, and Capsule Filling operations

Compliance with cGMP requirements

Handling eBMR, eBPR, and electronic logbooks

SAP/QMS operations and SCADA monitoring

3. Oral Solid Dosage (OSD) – Packing

Position: Officer / Senior Officer

Qualification: B.Pharm / B.Sc

Experience: 3–7 Years

Key Responsibilities

Primary and secondary packaging activities

Operation of automated packaging equipment

Documentation through eBPR and electronic log systems

Packaging process monitoring and compliance

4. OSD Manufacturing & Packing

Position: Associate

Qualification: 10th / 12th / ITI

Experience: 4–10 Years

Equipment Exposure Preferred

Glatt

ACG

Fette

Sejong

IMA-PG

BQ

Satellite Strip Machines

A300 Cartonator

Track & Trace Systems

5. Liquid Dosage Manufacturing

Position: Officer / Senior Officer / Executive

Qualification: B.Pharm

Experience: 1–9 Years

Key Responsibilities

Liquid manufacturing operations

Filling process management

Batch documentation and GMP compliance

Process monitoring and equipment handling

6. Liquid Dosage Manufacturing/Filling

Position: Associate

Qualification: 10th / 12th / ITI

Experience: 4–10 Years

Equipment Exposure Preferred

Autoclave operations

Filter Integrity Tester

Eye Drop Filling Machines

Ophthalmic Manufacturing Equipment

Sterile process handling

Documents Required

Candidates should carry:

Updated Resume/CV

Passport Size Photograph

Latest Salary Slip

Educational Certificates

Experience Documents

Why Join Ajanta Pharma?

Ajanta Pharma is recognized globally for its commitment to quality, innovation, and patient-focused healthcare solutions. The company offers excellent career growth opportunities, advanced manufacturing facilities, and exposure to international regulatory standards.

Professionals seeking opportunities in pharmaceutical manufacturing, quality control, packaging, and liquid dosage production can leverage this walk-in drive to advance their careers with a reputed pharmaceutical organization.

Technical FAQs

1. What is the difference between OOS and OOT in Quality Control?

OOS (Out of Specification) occurs when test results fall outside predefined acceptance criteria, while OOT (Out of Trend) refers to results that remain within specifications but deviate significantly from historical trends, requiring investigation.

2. Why is HPLC widely used in pharmaceutical Quality Control?

HPLC (High Performance Liquid Chromatography) provides accurate identification, quantification, and purity analysis of pharmaceutical compounds, making it essential for raw material, in-process, and finished product testing.

3. What is the role of SCADA in pharmaceutical manufacturing?

SCADA (Supervisory Control and Data Acquisition) enables real-time monitoring and control of manufacturing equipment, improving process consistency, data integrity, and regulatory compliance.

4. What is a Filter Integrity Test in sterile liquid manufacturing?

A Filter Integrity Test verifies that sterilizing-grade filters remain intact and effective before and after filtration, ensuring product sterility and compliance with GMP requirements.

5. Why are eBMR and eBPR important in pharmaceutical production?

Electronic Batch Manufacturing Records (eBMR) and Electronic Batch Packing Records (eBPR) improve data accuracy, reduce documentation errors, enhance traceability, and support compliance with regulatory guidelines such as FDA and EU GMP standards.