Ajanta Pharma has announced a walk-in interview for experienced pharmaceutical professionals at its US FDA-approved OSD formulation manufacturing facility located in Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra. The interview will be conducted in Vapi, Gujarat for multiple departments including Production, Maintenance, and Quality Assurance.
Candidates with relevant pharmaceutical manufacturing experience and the required educational qualifications are encouraged to attend the walk-in drive with all necessary documents.
Company Name: Ajanta Pharma Ltd.
Job Type: Walk-In Interview
Interview Date: 12 July 2026 (Sunday)
Interview Time: 10:00 AM to 4:00 PM
Interview Venue:
Hotel Woodland
N.H. No. 8, Near Desai Auto Mobiles, Balitha, Vapi, Gujarat – 396191
Manufacturing Location: Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
Production Officer / Sr. Officer
Qualification:
Experience:
Maintenance Officer / Sr. Officer
Qualification:
- BE / Diploma – Electrical
- BE / Diploma – Mechanical
Experience:
Quality Assurance Officer / Sr. Officer
Qualification:
Experience:
Production
- Handle OSD manufacturing operations including granulation, compression, coating, pellet coating, capsule filling and related activities.
- Work in primary and secondary packing sections.
- Maintain GMP documentation and production records.
- Operate and maintain systems including PAS, SCADA, E-Log and related manufacturing software.
- Participate in production planning, inventory control and qualification activities.
- Utilize tools such as Microsoft Excel, Power BI and AI-based production applications.
Maintenance
- Perform preventive and breakdown maintenance of pharmaceutical equipment.
- Handle PLC, SCADA and electrical control systems.
- Maintain utilities including HVAC, Humidifier and Dehumidifier AHU systems.
- Troubleshoot equipment and utility-related issues efficiently.
Quality Assurance
- Review batch manufacturing records and documentation.
- Perform IPQA activities during manufacturing and packing.
- Review analytical reports and laboratory records.
- Handle change control, CAPA, deviations, investigations and market complaints.
- Work with LIMS, eBMR, QMS and related quality systems.
Eligible candidates should possess any of the following qualifications:
- B.Pharm
- M.Pharm
- BE Electrical
- BE Mechanical
- Diploma Electrical
- Diploma Mechanical
Relevant experience in pharmaceutical manufacturing, especially in US FDA/MHRA-approved facilities, will be preferred.
- Knowledge of GMP and documentation practices
- Experience with PAS, SCADA, QMS, eBMR and LIMS
- Strong communication and teamwork skills
- Understanding of pharmaceutical manufacturing processes
- Good analytical and problem-solving abilities
Ajanta Pharma has not officially disclosed the salary.
Expected Salary Range: ₹3.5 LPA – ₹8.5 LPA (Approx.), depending on qualification, experience and interview performance.
- Opportunity to work in a US FDA-approved manufacturing facility
- Career growth in a leading pharmaceutical organization
- Learning and development opportunities
- Competitive compensation package
- Professional work environment
Candidates should bring:
- Updated CV/Resume
- Passport-size photographs
- Educational certificates
- Experience certificates
- Latest salary slips
- Government ID proof
Candidates currently working with USFDA/MHRA-approved pharmaceutical facilities are preferred. Applicants should carry copies of documents for interview verification.
Interested and eligible candidates can directly attend the walk-in interview on the scheduled date and venue.
Walk-In Date: 12 July 2026
Time: 10:00 AM – 4:00 PM
Candidates who are unable to attend the interview may send their updated CV to:
Email: CV.ptno@ajantapharma.com
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