About the Company
Ajanta Pharma Ltd. is a leading specialty pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality finished dosage formulations for domestic and international markets.
Recognized as a Great Place To Work® Certified 2026 organization, the company has established a strong reputation for innovation, quality, and regulatory excellence.
With seven state-of-the-art manufacturing facilities across India, Ajanta Pharma serves regulated and emerging global markets while maintaining strict compliance with international regulatory standards, including US FDA requirements.
The company continues to invest in advanced manufacturing technologies, digital systems, and employee development, making it one of the preferred employers in the Indian pharmaceutical industry.
Job Details
- Company Name: Ajanta Pharma Ltd.
- Departments: Production, Maintenance, Quality Assurance
- Experience: 1–8 years (varies by role)
- Qualification: B.Pharm, M.Pharm, BE, DEE (Diploma Engineering), Electrical Engineering, Mechanical Engineering
- Job Location: Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
- Interview Location: Vapi, Gujarat
- Work Type: On-site
- Industry: Pharmaceutical Manufacturing
- Facility: US FDA Approved OSD Formulation Plant
Job Description
Ajanta Pharma is hiring experienced professionals for its US FDA-approved Oral Solid Dosage (OSD) formulation manufacturing facility.
The recruitment drive covers Production, Maintenance, and Quality Assurance departments, offering excellent opportunities for professionals experienced in regulated pharmaceutical manufacturing.
Production Officer / Senior Officer
- Department: Production
- Role: Officer / Senior Officer
- Market: US FDA Regulated Manufacturing
- Experience: 1–3 years and 4–8 years
- Education/Qualification: B.Pharm / M.Pharm
Maintenance Officer / Senior Officer
- Department: Maintenance
- Role: Officer / Senior Officer
- Market: US FDA Regulated Manufacturing
- Experience: 2–3 years and 5–6 years
- Education/Qualification: BE / DEE in Electrical or Mechanical Engineering
Quality Assurance Officer / Senior Officer
- Department: Quality Assurance
- Role: Officer / Senior Officer
- Market: US FDA Regulated Manufacturing
- Experience: 4–8 years
- Education/Qualification: B.Pharm / M.Pharm
Skills & Qualifications
- B.Pharm or M.Pharm qualification for Production and QA roles.
- BE or Diploma Engineering in Mechanical/Electrical for Maintenance.
- Experience in OSD manufacturing operations.
- Knowledge of PAS-X, SCADA, and E-log systems.
- Understanding of cGMP and GDP documentation.
- Experience with equipment qualification and validation.
- Knowledge of QMS, CAPA, deviations, and change control.
- Familiarity with TRIMS, LIMS, OpenLab, and LC Solution.
- Experience in production planning and inventory management.
- Proficiency in Microsoft Excel, PowerPoint, and Power BI.
- Knowledge of HVAC, AHU, humidifier, and dehumidifier systems.
- Experience with PLC and electrical maintenance.
- Strong documentation and communication skills.
- Ability to work in regulated manufacturing environments.
- Exposure to US FDA or MHRA-approved facilities is preferred.
Key Responsibilities
- Perform OSD manufacturing operations.
- Handle granulation, compression, and coating activities.
- Operate capsule filling equipment.
- Maintain production documentation.
- Execute preventive maintenance activities.
- Resolve equipment breakdowns.
- Support utility equipment maintenance.
- Conduct equipment qualification activities.
- Review analytical and microbiological reports.
- Ensure compliance with QMS procedures.
- Manage deviations and CAPA.
- Support change control processes.
- Maintain cGMP and GDP compliance.
- Participate in production planning.
- Follow regulatory documentation standards.
Benefits/Perks
- Opportunity to work in a US FDA-approved facility.
- Career growth with a leading pharmaceutical company.
- Exposure to international regulatory standards.
- Modern manufacturing technologies.
- Learning and development opportunities.
- Collaborative work environment.
- Competitive compensation package.
- Long-term career stability.
- Global pharmaceutical exposure.
- Great Place To Work® certified organization.
How to Apply
Interested candidates currently working in US FDA or MHRA-approved manufacturing facilities are encouraged to attend the walk-in interview with the following documents:
- Updated resume/CV
- Current CTC structure
- Three recent salary slips
- Educational qualification certificates
- Previous employment documents
Candidates who cannot attend the walk-in interview may send their updated resume via email.
Official Email: [email protected]
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ajanta career page.
For more verified pharma jobs, walk-in interviews, and the latest QA jobs, QC jobs, and production jobs
Apply today and take the next step toward a rewarding pharmaceutical career with Ajanta Pharma.
Walk-in Interview Details
- Date: Sunday, 12 July 2026
- Time: 10:00 AM – 4:00 PM
- Venue: Hotel Woodland, NH No. 8, Near Desai Auto Mobiles, Balitha, Vapi, Gujarat – 396191
- Job Location: Paithan, District Chhatrapati Sambhajinagar (Aurangabad), Maharashtra
- Email: [email protected]
Why You Should Join Ajanta Pharma
Ajanta Pharma offers an excellent platform for professionals seeking long-term growth in the pharmaceutical industry. As a Great Place To Work® Certified company, it values innovation, quality, and employee development.
Employees gain hands-on experience with advanced manufacturing technologies while working in a highly regulated US FDA-compliant environment.
Continuous learning, structured career progression, and exposure to global pharmaceutical practices make Ajanta Pharma an ideal destination for ambitious professionals.
