Ajanta Pharma, a globally recognized pharmaceutical company operating in more than 30 countries, has announced a Walk-In Interview for its Dahej, Gujarat manufacturing facility. The company is inviting experienced professionals from Manufacturing, Packing, Quality Control (QC), Quality Assurance (QA), and Maintenance departments to join its growing team.

This recruitment drive offers excellent opportunities for candidates with experience in OSD (Oral Solid Dosage) manufacturing, quality systems, analytical testing, engineering maintenance, and regulatory compliance.

Company Details

• Company Name: Ajanta Pharma Ltd.
• Location: Dahej, Gujarat
• Interview Venue: Hotel Legend Sarovar Portico, Industrial Town of Baddi, Himachal Pradesh
• Interview Date: 11th October 2026 (Sunday)
• Interview Time: 09:00 AM to 04:00 PM

Open Positions

1. Manufacturing / Packing – Sr. Officer / Officer

Qualification:

• B.Pharm
• M.Pharm

Experience:

• 2 to 8 Years

Required Skills:

• Granulation
• Pellet Coating
• Capsule Filling
• Primary Packing
• Secondary Packing
• OOS/OOT Investigation
• Deviation Management
• Incident Investigation
• QMS Documentation

2. Manufacturing / Packing – Associate / Operator

Qualification:

• 10th / 12th Pass
• ITI
• Diploma
• D.Pharm
• B.A
• B.Com

Experience:

• 2 to 10 Years

Required Skills:

• Granulation
• Pellet Coating
• Capsule Manufacturing
• Blister Packing
• Sachet Filling
• Bottle Line Operations
• Cartoning & Labelling
• Secondary Packing Activities

3. Quality Control (QC) – Sr. Officer / Officer / Executive

Qualification:

• D.Pharm
• B.Sc
• M.Sc
• B.Pharm

Experience:

• 3 to 12 Years

Required Skills:

• Solid Oral Dosage Analysis
• FP Testing
• Instrumentation Handling
• Stability Studies
• Method Validation
• Dissolution Testing
• PMQC Activities
• QMS Compliance

4. Quality Assurance (QA) – Executive / Sr. Executive

Department:

• Production
• Quality Control
• Quality Assurance

Qualification:

• M.Sc
• B.Pharm
• M.Pharm

Experience:

• 8 to 13 Years

Required Skills:

• OOS Investigation
• OOT Investigation
• Deviation Handling
• Incident Management
• Risk Assessment
• Impact Assessment
• Quality System Compliance

5. Maintenance (QMS / Qualification) – Sr. Officer / Officer

Qualification:

• B.E. Mechanical
• B.E. Instrumentation

Experience:

• 4 to 10 Years

Required Skills:

• SOP Preparation
• Change Control
• Deviation Management
• CAPA Handling
• URS, DQ, IQ, OQ & PQ Documentation
• e-Log Systems
• Qualification Activities

6. Maintenance (HVAC) – Sr. Officer / Officer

Qualification:

• B.E. Electrical

Experience:

• 2 to 10 Years

Required Skills:

• HVAC Maintenance
• Preventive Maintenance
• Breakdown Maintenance
• Troubleshooting
• Plant Equipment Inspection
• Condition Monitoring
• Spare Parts Management
• Regulatory Audit Support

Interview Documents Required

Candidates should carry:

• Updated Resume/CV
• Recent Passport Size Photograph
• Current CTC Details
• Salary Breakup Documents
• Educational Certificates
• Experience Certificates
• Government ID Proof

Email for CV Submission

Candidates unable to attend the interview can send their updated CV to:

referral.dhj@ajantapharma.com

Why Join Ajanta Pharma?

• Great Place to Work Certified Organization
• Global Pharmaceutical Presence
• Advanced Manufacturing Facility
• Career Growth Opportunities
• Exposure to International Regulatory Standards
• Learning-Oriented Work Environment

Technical FAQs

1. What is OOS and OOT in pharmaceutical manufacturing?

OOS (Out of Specification) occurs when a test result falls outside approved specifications, while OOT (Out of Trend) refers to unusual results that are within limits but differ significantly from historical trends.

2. What is the purpose of IQ, OQ, and PQ in equipment qualification?

• IQ (Installation Qualification): Confirms correct installation.
• OQ (Operational Qualification): Verifies operational performance.
• PQ (Performance Qualification): Confirms consistent performance under actual production conditions.

3. Why is method validation important in Quality Control?

Method validation ensures analytical methods are accurate, precise, specific, robust, and suitable for their intended purpose, ensuring reliable test results.

4. What is CAPA in pharmaceutical quality systems?

CAPA (Corrective and Preventive Action) is a systematic approach used to identify root causes of deviations, implement corrective actions, and prevent recurrence.

5. What are the key responsibilities of HVAC systems in pharmaceutical plants?

HVAC systems maintain temperature, humidity, air cleanliness, differential pressure, and contamination control to ensure GMP compliance and product quality.