Ajanta Walk-In Production, QA, QC, Maintenance & Warehouse

Ajanta Pharma Walk-In 2026 | QA QC Production Jobs

Ajanta Pharma hiring for Production, QA, QC, Maintenance & Warehouse roles in Dahej. ITI, B.Pharm, MSc candidates can apply.

Ajanta Pharma has announced a large-scale walk-in interview drive for experienced pharmaceutical professionals for its Dahej manufacturing facility in Gujarat. The company is hiring candidates for Manufacturing, Packing, Maintenance, Warehouse, Quality Control, and Quality Assurance departments.

This pharma recruitment drive is scheduled for 24 May 2026 in Daman and offers strong career opportunities for candidates looking for pharmaceutical manufacturing jobs, QA QC pharma jobs, maintenance engineering roles, warehouse positions, and regulated plant opportunities in India.

Candidates with experience in OSD manufacturing operations, pharmaceutical production, packing line maintenance, analytical quality control, validation, GMP documentation, and USFDA-regulated plant operations are encouraged to attend the interview.

Ajanta Pharma is one of the recognized pharmaceutical companies operating globally and continues expanding its workforce across regulated manufacturing facilities. Professionals searching for pharma jobs in Gujarat, production jobs in pharmaceutical companies, QC analyst roles, engineering jobs in pharma industry, and warehouse operator positions can explore these openings.

Company Overview

Ajanta Pharma is a specialty pharmaceutical company known for manufacturing and supplying quality medicines across more than 30 countries worldwide. The organization has built a strong presence in branded generics, specialty formulations, and regulated pharmaceutical manufacturing.

The company operates advanced pharmaceutical manufacturing facilities that focus on:

• OSD manufacturing operations
• Pharmaceutical packing systems
• Quality assurance and quality control
• Engineering maintenance
• Warehouse and inventory management
• Regulatory compliance
• GMP manufacturing systems
• USFDA-compliant operations

Ajanta Pharma continues investing in manufacturing excellence, pharmaceutical technology, and skilled workforce development.

Professionals working in regulated pharmaceutical plants gain exposure to:

• GMP compliance systems
• Validation and qualification activities
• Pharmaceutical documentation practices
• Regulatory audits
• Analytical quality systems
• Manufacturing process optimization
• Engineering maintenance systems
• Packaging line operations

This experience significantly improves long-term career opportunities in the pharmaceutical and healthcare manufacturing industry.

Job Role & Responsibilities

Ajanta Pharma is hiring for multiple departments and technical positions.

Manufacturing and Packing – Associate/Operator

The company is hiring Manufacturing and Packing Associates/Operators for OSD manufacturing operations.

Key Responsibilities

• Handling granulation operations
• Managing pellet coating activities
• Compression machine operations
• Coating process monitoring
• Capsule filling operations
• Blister packing operations
• Sachet filling activities
• Secondary packing and cartonator operations
• Maintaining GMP documentation
• Monitoring batch manufacturing processes
• Following SOPs and quality procedures

Candidates with experience in pharmaceutical formulation plants and OSD operations will have an advantage.

Manufacturing/Packing – Senior Officer/Officer

Experienced pharmaceutical professionals are also being hired for officer-level production roles.

Responsibilities Include

• Supervising production activities
• Monitoring pharmaceutical manufacturing operations
• Managing primary and secondary packing
• Coordinating with QA and QC departments
• Ensuring compliance with GMP standards
• Reviewing manufacturing records
• Handling process troubleshooting
• Maintaining production efficiency
• Supporting audit compliance activities

Candidates currently working in USFDA-approved plants are preferred.

Maintenance (Plant Maintenance)

Ajanta Pharma is hiring maintenance professionals for pharmaceutical plant maintenance operations.

Key Responsibilities

• Preventive maintenance of pharmaceutical equipment
• Troubleshooting manufacturing machines
• Handling packing line maintenance
• Supporting utility systems
• Equipment servicing and repair
• Managing electrical maintenance systems
• Supporting engineering documentation
• Maintaining compliance records

Equipment Experience Preferred

• Granulation equipment
• Compression machines
• Coating machines
• Pellet coating systems
• Blister packing machines
• Strip packing lines
• Powder packing systems
• Bulk packing lines

Strong technical understanding of pharmaceutical machinery is essential for these roles.

Maintenance (Utility) – Executive

The utility maintenance team will manage critical pharmaceutical utility systems.

Key Responsibilities

• Handling air compressors
• Managing chiller systems
• Monitoring boiler operations
• Supporting purified water systems
• Managing engineering qualification activities
• Maintaining GMP engineering documentation
• Handling CAPA, deviations, and change control
• Supporting URS, DQ, IQ, OQ, and PQ activities

Candidates with pharmaceutical utility maintenance experience are preferred.

Stores (Warehouse) – Associate/Operator

Warehouse professionals will manage pharmaceutical inventory and material operations.

Responsibilities Include

• Handling raw material inventory
• Managing packing material stock
• Supporting finished goods operations
• Maintaining warehouse documentation
• Coordinating inventory movement
• Following GMP storage practices
• Supporting dispatch and material tracking

Candidates currently working in pharmaceutical formulation warehouses are preferred.

Quality Control – Senior Officer/Officer

The Quality Control department is hiring experienced analytical professionals.

QC Responsibilities

• Analysis of solid oral formulations
• Handling analytical instrumentation
• In-process testing
• Stability sample analysis
• Analytical method validation
• PMQC operations
• Dissolution testing
• Laboratory documentation
• GMP and GLP compliance

Candidates with strong analytical chemistry and pharmaceutical laboratory experience will find good growth opportunities.

Quality Assurance – Senior Officer/Officer

The QA department will focus on pharmaceutical quality systems and compliance.

QA Responsibilities

• Validation activities
• Qualification protocols
• Investigation handling
• Engineering QA support
• Documentation review
• GMP compliance monitoring
• Audit preparation support
• Quality management system activities

Candidates with exposure to regulated manufacturing environments are preferred.

Eligibility / Qualifications

Educational Qualifications

Candidates with the following qualifications are eligible:

Manufacturing/Packing

• 10th Pass
• 12th Pass
• ITI
• Diploma
• D.Pharm
• B.Pharm
• M.Pharm

Maintenance

• B.E Electrical
• B.E Mechanical
• ITI Electrical
• Diploma Electrical

Quality Control

• B.Sc
• M.Sc
• D.Pharm
• B.Pharm

Quality Assurance

• B.Pharm
• M.Pharm

Relevant Courses

Pharmacy, Pharmaceutical Sciences, Industrial Pharmacy, Analytical Chemistry, Organic Chemistry, Electrical Engineering, Mechanical Engineering, Industrial Engineering, Chemical Engineering, Instrumentation, Life Sciences, Pharmaceutical Manufacturing Technology

Experience Required

• 2 to 10 years for most positions
• 10 to 12 years for Utility Executive role

Preferred Skills

Ajanta Pharma prefers candidates with:

• OSD manufacturing experience
• USFDA plant exposure
• GMP documentation knowledge
• Pharmaceutical packing experience
• Validation and qualification exposure
• Analytical instrumentation knowledge
• Utility maintenance expertise
• Warehouse operations experience

Location & Salary

Job Location

Dahej, Gujarat

Walk-In Venue

Hotel Reevanta, Teen Batti, Devka Road, Nani Daman

Approximate Salary Range

Based on current pharmaceutical industry standards in Gujarat, approximate salary ranges may include:

• Associate/Operator: ₹2.5 LPA – ₹4.5 LPA
• Officer/Sr. Officer: ₹4.5 LPA – ₹8 LPA
• Executive Roles: ₹8 LPA – ₹12 LPA

Final salary depends on:

• Experience level
• Technical expertise
• USFDA plant exposure
• Current CTC
• Department specialization

Professionals with regulated plant experience and strong pharmaceutical compliance knowledge often receive better compensation packages.

Application Process

Interested candidates can directly attend the walk-in interview.

Interview Details

• Date: 24 May 2026 (Sunday)
• Time: 09:00 AM to 04:00 PM

Documents Required

Candidates should carry:

• Updated Resume
• Latest CTC Breakup
• Passport Size Photograph
• Educational Certificates
• Experience Documents
• ID Proof

Email for Resume Submission

Candidates unable to attend the interview can send their updated CV to:

referral.dhj@ajantapharma.com

Additional Facility

AC Bus facility is available from:

• Bharuch
• Ankleshwar
• Vadodara

for candidates joining the Dahej location.

Why Pharma Manufacturing Jobs Are Growing in India

India continues to remain one of the world’s largest pharmaceutical manufacturing hubs.

Pharmaceutical companies are actively expanding hiring across:

• OSD manufacturing
• API manufacturing
• Pharmaceutical engineering
• Validation and compliance
• Quality assurance
• Quality control laboratories
• Warehouse and logistics operations
• Packaging and serialization systems

Professionals with regulated plant exposure and GMP knowledge are in high demand because companies serving regulated global markets require experienced manufacturing and compliance teams.

Pharma professionals working in USFDA-approved facilities also gain valuable experience that supports long-term career growth in:

• Pharmaceutical operations management
• Regulatory affairs
• Validation and compliance
• Manufacturing leadership
• Technical services
• Engineering management

FAQs

1. Which company is conducting this walk-in interview?

Ajanta Pharma is conducting the walk-in drive for its Dahej manufacturing facility.

2. Which departments are hiring?

Manufacturing, Packing, Maintenance, Warehouse, Quality Control, and Quality Assurance departments are hiring.

3. What experience is required?

Most positions require 2 to 10 years of pharmaceutical industry experience.

4. Is USFDA plant experience preferred?

Yes, candidates currently working in USFDA-approved plants are preferred for several roles.

5. What is the work location?

The job location is Dahej, Gujarat.

6. Can candidates send resumes by email?

Yes, candidates unable to attend the interview can email their resumes to referral.dhj@ajantapharma.com.

Summary Table

Company	Ajanta Pharma
Department Vacancies	Manufacturing, Packing, Maintenance, QC, QA, Warehouse
Qualification	10th, 12th, ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, B.Sc, M.Sc
Experience	2–12 Years
Location	Dahej, Gujarat