India's DMPLOI - Jobs & Networking AppAjanta Pharma, one of India’s leading specialty pharmaceutical companies with a presence in more than 30 countries, has announced a Walk-In Interview for multiple positions at its Dahej, Gujarat manufacturing facility. This recruitment drive offers excellent career opportunities for experienced professionals in Manufacturing, Packing, Quality Assurance, Quality Control, Maintenance, Stores, and Information Technology.
Candidates meeting the eligibility criteria are invited to attend the walk-in interview with their updated resume and required documents.
Company Overview
Company Name: Ajanta Pharma Ltd.
Industry: Pharmaceutical (Formulation Manufacturing)
Job Type: Walk-In Interview
Work Location: Dahej, Gujarat
Ajanta Pharma is recognized for manufacturing high-quality pharmaceutical products and operates globally with advanced manufacturing facilities that comply with international regulatory standards.
Walk-In Interview Details
Interview Date: 19th July 2026 (Sunday)
Time: 09:00 AM to 04:00 PM
Venue: Ginger Bharuch, Hotel Sethna Plaza Annex, 01 Station Road, Bharuch, Gujarat
Documents Required
Updated Resume
Recent Passport Size Photograph
Latest CTC Breakup
Educational Certificates
Experience Documents
Government ID Proof
Department-wise Vacancy Details
1. Manufacturing / Packing – Associate / Operator
Qualification
10th / 12th
ITI
Diploma
D.Pharm (Mandatory)
Experience
2–10 Years
Required Skills
OSD Manufacturing
Granulation
Pellet Coating
Compression
Coating
Capsule Manufacturing
Blister Packing
Sachet Filling
Secondary Packing
Cartonator
Labelling Operations
2. Maintenance (Plant Maintenance) – Sr. Officer / Officer
Qualification
B.E. (Electrical / Mechanical)
Experience
2–10 Years
Skills
Preventive Maintenance
Breakdown Maintenance
Equipment Troubleshooting
Plant Inspection
Condition Monitoring
Documentation Compliance
Spare Parts Management
Regulatory Audit Exposure
3. Maintenance (Plant Maintenance) – Assistant
Qualification
ITI / Diploma (Fitter / Electrical / Mechanical)
Experience
2–10 Years
Skills
Preventive & Breakdown Maintenance
Troubleshooting
Equipment Inspection
Condition Monitoring
Spare Parts Management
Documentation Compliance
4. Stores (Warehouse) – Officer / Associate (Operator)
Qualification
Any Graduate (Officer)
ITI / D.Pharm (Associate/Operator)
Experience
4–10 Years
Skills
Raw Material Handling
Packing Material Management
Finished Goods (FG)
Pharma Warehouse Operations
Inventory Control
5. Information Technology – Officer / Executive
Qualification
BCA
MCA
BE (IT)
BE (Instrumentation)
Experience
2–10 Years
Skills
IPC & SCADA
Documentation
CSV Support
Data Backup
Server Management
GxP Systems
Network Management
QMS Activities
6. Quality Control – Sr. Officer / Officer
Qualification
B.Sc.
M.Sc.
B.Pharm
Experience
3–8 Years
Skills
Solid Oral Analysis
Instrumentation
In-process Testing
Stability Studies
Analytical Method Validation
PMQC
Dissolution Testing
7. Quality Assurance – Sr. Officer / Officer
Qualification
B.Pharm
M.Pharm
Experience
3–5 Years
Skills
Validation
Qualification
DRA
ITQA
Investigation
Engineering QA
USFDA Regulatory Compliance
Employee Benefits
Opportunity to work with a leading pharmaceutical company.
Exposure to regulated manufacturing facilities.
Professional career growth.
AC bus facility available from Bharuch, Ankleshwar, and Vadodara to the Dahej plant.
Why Join Ajanta Pharma?
Global pharmaceutical organization with operations in 30+ countries.
Modern manufacturing facilities.
Regulatory-compliant work environment.
Excellent learning and career development opportunities.
Exposure to USFDA and international quality systems.
Technical FAQs
1. What is OSD manufacturing in the pharmaceutical industry?
OSD (Oral Solid Dosage) manufacturing involves producing tablets, capsules, and related oral medicines through processes such as granulation, blending, compression, coating, and packing.
2. What is Analytical Method Validation (AMV)?
Analytical Method Validation is the documented process of proving that an analytical test method consistently produces accurate, precise, specific, and reliable results according to regulatory guidelines.
3. What is the role of QMS in pharmaceutical manufacturing?
A Quality Management System (QMS) ensures compliance with GMP regulations by controlling documentation, deviations, CAPA, change control, training, and quality audits.
4. What is preventive maintenance in pharmaceutical plants?
Preventive maintenance is the scheduled servicing and inspection of equipment to reduce unexpected breakdowns, improve machine reliability, and ensure uninterrupted production.
5. What is CSV (Computer System Validation)?
Computer System Validation (CSV) is the process of verifying that computerized systems used in pharmaceutical manufacturing consistently perform as intended and comply with regulatory requirements such as GxP and FDA guidelines.
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