Ajanta Pharma is Hiring for Manufacturing, QA, QC, and Production Roles | Walk-in Interview on 14th Dec 2025

Discover top pharma jobs at Ajanta Pharma. Attend our walk-in for manufacturing, QA, QC, and production roles in Dahej. Elevate your pharmaceutical careers in India now!

About the Company

Ajanta Pharma Limited, a leading specialty pharmaceutical company founded in 1973, delivers high-quality, affordable medicines to over 30 countries worldwide. With a strong focus on ophthalmology, dermatology, and cardiology therapies, Ajanta holds leadership positions in multiple markets through its branded generics portfolio.

Its state-of-the-art manufacturing facilities in Dahej, Gujarat, adhere to global standards like USFDA, EU-GMP, and WHO certifications, emphasizing innovation, sustainability, and regulatory compliance.

Committed to growth, Ajanta invests in renewable energy—aiming for 70% solar sourcing by FY 2027—while fostering a certified Great Place to Work culture that drives employee excellence and global expansion.

Job Details

• Company Name: Ajanta Pharma Limited
• Experience: 2 to 10 years
• Qualification: 10th/12th+ITI, Diploma, D.Pharm, B.Sc./M.Sc., B.Pharm/M.Pharm, B.E (Electrical), Any Graduate
• Location: Dahej, Gujarat (Walk-in at Vapi)
• Work Type: On-site

Job Description

Ajanta Pharma is expanding its Dahej facility with walk-in opportunities across manufacturing, quality, production, and maintenance functions. These roles prioritize GMP-compliant operations in solid oral dosage (OSD) forms, offering hands-on impact in a global pharma leader.

Ideal for professionals seeking stable pharmaceutical careers in India with exposure to regulated markets.

Manufacturing/Packing Associate/Operator

• Department: Manufacturing/Packing
• Role: Execute OSD operations and packing
• Experience: 2 to 10 years
• Education/Qualification: 10th, 12th+ITI, Diploma, D.Pharm (Mandatory)

Quality Control – Sr. Officer/Officer

• Department: Quality Control
• Role: Analyze and validate OSD samples
• Experience: 2 to 8 years
• Education/Qualification: B.Sc./M.Sc./B.Pharm/M.Pharm

Manufacturing/Packing Sr. Officer/Officer

• Department: Manufacturing/Packing
• Role: Oversee OSD production and packing
• Experience: 2 to 8 years
• Education/Qualification: B.Pharm/M.Pharm

Quality Assurance Sr. Officer/Officer

• Department: Quality Assurance
• Role: Manage audits and validations
• Experience: 3 to 8 years
• Education/Qualification: B.Pharm/M.Pharm

Production (MES (PAS X) – Sr. Officer/Officer

• Department: Production – MES (PAS X)
• Role: Design and troubleshoot manufacturing systems
• Experience: 2 to 8 years
• Education/Qualification: B.Pharm/M.Pharm/B.E

Stores (Warehouse) – Sr. Officer/Officer

• Department: Stores/Warehouse
• Role: Handle raw and packing materials
• Experience: 3 to 10 years
• Education/Qualification: Any Graduate

Maintenance – Sr. Officer/Officer/Assistant (For Plant Maintenance/HVAC)

• Department: Maintenance
• Role: Maintain equipment and HVAC systems
• Experience: 3 to 10 years
• Education/Qualification: B.E (Electrical); For Assistant – ITI (Electrical)

Skills/Qualifications

• Exposure to OSD manufacturing: granulation, pellet coating, compression, capsule filling
• Proficiency in primary/secondary packing: blister, sachet, cartonator, labelling
• Analytical expertise in FP, RM, in-process, stability testing; PMQC and dissolution
• Knowledge of AQA, APQR preparation, validation, IPQA protocols
• Experience with MES (PAS X): MBR designing, troubleshooting, PCS integration
• Warehouse management in pharma formulations for raw/packing materials
• GMP documentation and maintenance of granulation, compression, coating machines
• e-BPR, e-log systems; method validation for regulated compliance

Key Responsibilities

• Operate and monitor OSD production lines
• Perform quality analysis and stability checks
• Execute packing and validation processes
• Design MBRs and integrate MES systems
• Manage warehouse inventory accurately
• Maintain equipment per GMP standards
• Conduct audits and prepare APQRs

Benefits/Perks

• Career growth in a Great Place to Work environment
• Continuous learning via skill enhancement programs
• Competitive salary with performance incentives
• Supportive culture fostering innovation
• Global exposure across 30+ countries

How to Apply

Attend the walk-in interview with your latest resume, CTC breakup, and passport-size photo. If unable to attend, email your updated CV to referral.dhj@ajantapharma.com. AC bus available from Bharuch, Ankleshwar, Vadodara.

For more pharma jobs, visit https://pharmarecruiter.in. Apply today—join Ajanta’s legacy of excellence!

Walk-in Interview Details

• Date: 14th December 2025 (Sunday)
• Time: 09:00 AM to 04:00 PM
• Venue: Hotel Silver Leaf, Plot No-CM-14 & 15, Raghuvir Complex, Opp. Vapi Industries, Vapi
• Contact/Email: referral.dhj@ajantapharma.com

Note: Candidates who appeared in the last 6 months are not eligible.

Why You Should Join

Joining Ajanta Pharma means embracing a certified Great Place to Work culture of recognition and innovation, where your skills in OSD manufacturing and quality drive medicines to 30+ countries.

With robust career stability from USFDA-approved facilities and sustainable growth initiatives, unlock endless learning opportunities in a compliance-focused ecosystem. Thrive in Dahej’s dynamic pharma hub, balancing professional advancement with collaborative excellence in India’s global pharmaceutical landscape.

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