India's DMPLOI - Jobs & Networking AppAjanta Pharma Limited has announced a Walk-In Interview for experienced professionals in the Production and Maintenance departments. The recruitment is for its US FDA-approved OSD (Oral Solid Dosage) Formulation Manufacturing Facility located at Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra. The interview will be conducted in Indore on 05 July 2026 (Sunday).
This is an excellent opportunity for candidates with pharmaceutical manufacturing experience to join one of India’s leading pharmaceutical companies.
Job Overview
Particular Details
Company
Ajanta Pharma Ltd.
Job Type
Walk-In Interview
Interview Date
05 July 2026 (Sunday)
Time
10:00 AM – 4:00 PM
Interview Location
Papaya Tree Hotel, Rau-Indore, Indore, Madhya Pradesh
Work Location
Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
Facility
US FDA Approved OSD Formulation Plant
Departments & Eligibility
1. Production Department
Position
Officer
Senior Officer
Qualification
B.Pharm
M.Pharm
M.Pharm + MBA
Experience: 1–3 Years
Candidates should have experience in:
Granulation
Compression
Coating
Pellet Coating
Capsule Filling
PAS-X
SCADA
Primary & Secondary Packing
e-Log
Track & Trace
e-BMR
Experience: 4–8 Years
Candidates should have knowledge of:
OSD Manufacturing
QMS
Training Activities
Equipment Qualification
PAS-X
TRIMS
Production Planning
Inventory Control
Advanced Microsoft Excel
PowerPoint
Power BI
AI-based productivity tools
2. Maintenance Department
Position
Officer
Senior Officer
Qualification
BE
Diploma in Electrical Engineering (DEE)
Specialization
Mechanical
Electrical
Experience
4–8 Years
Required Skills
Candidates should have experience in:
Preventive Maintenance
Breakdown Maintenance
PLC
SCADA
Electrical Panels
e-Log
Utility Equipment
HVAC System
AHU
Humidifier & Dehumidifier
ETP
STP
Software troubleshooting will be an added advantage.
Documents Required
Carry the following documents:
Updated Resume/CV
Educational Certificates
Experience Certificates
Latest CTC Proof
Passport Size Photograph
Unable to Attend?
Candidates who cannot attend the walk-in interview can send their updated CV to:
Email: cv.ptn@ajantapharma.com
Important Notes
Candidates having exposure to cGMP/GDP documentation and working in regulated pharmaceutical plants will be preferred.
Professionals currently working in USFDA/MHRA approved facilities are encouraged to attend.
Carry your latest CV, educational certificates, recent CTC structure, last three salary slips, and previous employment documents.
Why Join Ajanta Pharma?
Great Place to Work Certified (2026)
US FDA Approved Manufacturing Facility
Modern OSD Manufacturing Environment
Career Growth Opportunities
Exposure to Global Regulatory Standards
Learning & Development Programs
Technical FAQs
1. What is OSD manufacturing in the pharmaceutical industry?
OSD (Oral Solid Dosage) manufacturing involves the production of tablets, capsules, pellets, and other solid oral medicines through processes such as granulation, compression, coating, capsule filling, and packaging.
2. What is PAS-X and why is it important?
PAS-X is a Manufacturing Execution System (MES) widely used in pharmaceutical plants for electronic batch records (eBMR), production monitoring, and ensuring compliance with regulatory requirements like US FDA 21 CFR Part 11.
3. What is SCADA used for in pharmaceutical manufacturing?
SCADA (Supervisory Control and Data Acquisition) is an industrial automation system used to monitor and control manufacturing equipment, collect production data, and improve operational efficiency.
4. What is Equipment Qualification (EQ)?
Equipment Qualification is the documented process of verifying that pharmaceutical equipment is installed, operated, and performs consistently according to predefined specifications through IQ, OQ, and PQ protocols.
5. Why are HVAC, AHU, ETP, and STP systems important in pharma plants?
These systems help maintain controlled environmental conditions, ensure clean manufacturing areas, manage wastewater treatment, and support GMP compliance to protect product quality and patient safety.
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