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Ajanta Pharma Limited is conducting a large-scale walk-in interview at its Pithampur manufacturing facility, offering strong career opportunities for experienced professionals in Quality Assurance, Quality Control, and Warehouse functions. This hiring drive is aimed at strengthening regulated manufacturing operations and provides exposure to advanced quality systems, compliance-driven processes, and a stable pharmaceutical work environment. Candidates with relevant experience in OSD manufacturing and regulatory plants are encouraged to attend this on-site walk-in interview.
About the Company
Ajanta Pharma Limited is a well-established Indian pharmaceutical company known for delivering high-quality finished dosage formulations across domestic and international markets. The company operates multiple manufacturing facilities approved by global regulatory authorities such as USFDA and MHRA, reflecting its strong compliance culture and commitment to quality. Ajanta Pharma specializes in branded generics and formulations across therapeutic segments and follows stringent GMP practices, robust documentation systems, and continuous improvement through quality management systems. Its manufacturing sites are supported by advanced laboratories, trained professionals, and a strong regulatory mindset aligned with global pharmaceutical standards.
Job Details
• Company Name: Ajanta Pharma Limited
• Job Type: Walk-in Interview, On-site
• Experience Required: 2 to 12 years depending on department and role
• Qualification: BPharm/MPharm/BSc/MSc/Any Graduate
• Location: Pithampur Unit, Indore District, Madhya Pradesh
• Work Profile: Quality Assurance/Quality Control/Warehouse
Job Description
Quality Assurance
• Experience: 3 to 12 years depending on section
• Qualification: BPharm/MPharm/BSc/MSc
• Work Areas/Sections: Lab QA pre-checks, online review, data review, control sample management, investigations, IPQA line clearance, manufacturing and packing process checks, batch record review, deviation and incident handling, validation activities, cleaning validation, hold time studies, QMS documentation, change control, CAPA, qualification and requalification
✔ Strong exposure to regulated environments such as USFDA and MHRA
✔ Experience in OSD manufacturing preferred
Quality Control
• Experience: 3 to 12 years depending on section
• Qualification: BPharm/MPharm/BSc/MSc
• Work Areas/Sections: GLP operations, stability studies, raw material analysis, finished product and packing material testing, water sampling and analysis, environmental monitoring, microbiological testing, HPLC, UV, dissolution, DT, GC, KF, IR, ICPMS, method transfer, LIMS and Chromeleon handling
✔ Stability experience of minimum 3 years required for SEZ units
✔ Experience in OSD manufacturing environment preferred
Warehouse
• Experience: 2 to 4 years
• Qualification: Any Graduate (BCom/BSc/BA or equivalent)
• Work Areas/Sections: Raw material receipt, dispensing operations, SAP transactions, documentation handling, inventory coordination
✔ Knowledge of RM handling and dispensing processes
✔ Good communication and coordination skills required
Skills/Qualifications
• Strong understanding of OSD manufacturing and quality operations
• Practical knowledge of GMP, GLP, data integrity, and regulatory documentation
• Hands-on exposure to analytical instruments, validation protocols, and quality systems
• Awareness of cleanroom practices, safety standards, and compliance requirements
• Good communication skills and ability to work in cross-functional teams
Key Responsibilities
• Performing and reviewing quality checks across manufacturing and laboratory operations
• Ensuring compliance with GMP, safety, and regulatory guidelines
• Executing validation, qualification, and stability activities as per protocols
• Handling deviations, investigations, CAPA, and change management processes
• Supporting audits, inspections, and regulatory submissions
• Coordinating with QA, QC, production, and warehouse teams for smooth operations
How to Apply
Eligible candidates should attend the walk-in interview in person. Candidates must carry an updated resume, current compensation letter, educational certificates, experience documents, and one passport-size photograph. Only candidates meeting experience criteria should attend the interview.
Walk-in Interview Details
• Date: Friday, 30 January 2026 (Quality Control) and Saturday, 31 January 2026 (Quality Assurance and Warehouse)
• Time: 10:00 AM to 03:00 PM
• Venue: Ajanta Pharma Limited, Plot No. 55, 56, 57 ISEZ, Phase II, Pithampur, District Dhar, Madhya Pradesh – 454775
Why You Should Join
• Opportunity to work in a globally regulated pharmaceutical environment
• Exposure to advanced quality systems and compliance-driven operations
• Strong learning and professional development culture
• Stable career growth in a reputed pharmaceutical organization
• Collaborative work environment with experienced technical teams
FAQs
What departments are hiring in this walk-in interview?
Quality Assurance, Quality Control, and Warehouse departments are hiring.
What is the experience range required for these roles?
Experience ranges from 2 to 12 years depending on department and section.
Which qualifications are eligible for these jobs?
BPharm, MPharm, BSc, MSc are required for QA and QC roles, while any graduate is eligible for Warehouse roles.
Is experience in regulated plants mandatory?
Yes, working exposure in USFDA and MHRA regulated environments is required.
Are freshers eligible for this walk-in interview?
No, these openings are for experienced candidates only.
Is stability experience mandatory for Quality Control roles?
Yes, a minimum of 3 years stability experience is required for SEZ Pithampur units.
What type of manufacturing experience is preferred?
Candidates with experience in OSD manufacturing will be preferred.
What documents should be carried for the interview?
Updated resume, current compensation letter, educational and experience certificates, and a passport-size photograph.
Can candidates who appeared recently attend again?
Candidates who appeared for an interview in the last 6 months are not eligible.
What is the work location for selected candidates?
The work location will be Ajanta Pharma Limited’s Pithampur manufacturing unit in Madhya Pradesh.