India's DMPLOI - Jobs & Networking AppAjanta Pharma Ltd. is inviting applications from talented and experienced professionals for its US FDA-approved OSD Formulation Manufacturing Facility located at Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra. The company is conducting a Walk-In Interview at Vapi, Gujarat for multiple positions in Production, Maintenance, and Quality Assurance departments.
If you are looking to build your career with one of India’s leading pharmaceutical companies, this is an excellent opportunity to join a globally recognized organization certified as a Great Place to Work 2026.
Job Details
Company Name: Ajanta Pharma Ltd.
Interview Type: Walk-In Interview
Manufacturing Facility: US FDA Approved OSD Formulation Plant, Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
Interview Location: Hotel Woodland, NH-8, Near Desai Auto Mobiles, Balitha, Vapi, Gujarat – 396191
Interview Date: Sunday, 12 July 2026
Interview Time: 10:00 AM to 4:00 PM
Departments & Vacancies
1. Production
Position: Officer / Sr. Officer
Qualification:
- B.Pharm / M.Pharm
Experience:
- 1–3 Years
- 4–8 Years
Key Responsibilities
- OSD manufacturing operations including granulation, compression, coating, pellet coating and capsule filling.
- Primary & secondary packing operations.
- Knowledge of PAS-X, SCADA, E-Log, Track & Trace and eBMR.
- Production planning and inventory control.
- Equipment qualification.
- QMS documentation.
- Good knowledge of MS Excel, PowerPoint, Power BI and AI tools.
2. Maintenance
Position: Officer / Sr. Officer
Qualification:
- BE / DEE (Electrical / Mechanical)
Experience:
- 4–8 Years
Key Responsibilities
- Preventive and breakdown maintenance of process equipment.
- Knowledge of PLC, SCADA, electrical panels and E-Log.
- Utility equipment maintenance including ETP & STP.
- HVAC, Humidifier and Dehumidifier AHU maintenance.
- Software troubleshooting experience will be an added advantage.
3. Quality Assurance (QA)
Position: Officer / Sr. Officer
Qualification:
- B.Pharm / M.Pharm
Experience:
- 2–3 Years
- 5–6 Years
Key Responsibilities
- IPQA activities in manufacturing and packing.
- Equipment qualification and validation.
- Analytical QA and review of analytical reports.
- GLP compliance and QC instrument software qualification.
- LIMS/OpenLab/LC solution handling.
- QMS activities including CAPA, Change Control, Deviations, Incidents and Market Complaints.
Preferred Candidates
- Candidates with exposure to cGMP/ GDP documentation and regulated pharmaceutical manufacturing plants.
- Professionals currently working in USFDA/MHRA-approved facilities will be preferred.
Documents Required
Candidates should carry:
- Updated CV/Resume
- Current CTC details
- Last 3 Salary Slips
- Educational Certificates
- Previous Employment Documents
Unable to Attend?
Candidates who cannot attend the walk-in interview can send their updated CV to:
Why Join Ajanta Pharma?
- US FDA-approved OSD manufacturing facility
- Excellent career growth opportunities
- Exposure to international regulatory standards
- Work with advanced pharmaceutical manufacturing technologies
- Certified Great Place to Work 2026
Interview Date & Time
Sunday, 12 July 2026 | 10:00 AM – 4:00 PM | Hotel Woodland, Vapi, Gujarat
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