Ajanta Pharma Ltd., one of India’s leading pharmaceutical companies with a US FDA-approved formulation manufacturing facility, has announced a recruitment drive for experienced professionals at its Paithan plant in Chhatrapati Sambhajinagar (Aurangabad), Maharashtra. The company is inviting applications for EHS, PPIC, and IT departments.

This opportunity is ideal for candidates with experience in pharmaceutical manufacturing, production planning, environmental health & safety, and IT support who are looking to build their careers in a globally recognized pharmaceutical organization.

About Ajanta Pharma

Ajanta Pharma Ltd. is a multinational pharmaceutical company engaged in the development, manufacturing, and marketing of quality specialty pharmaceutical products. The company operates US FDA, WHO-GMP, and other internationally approved manufacturing facilities and exports medicines to more than 30 countries worldwide.

Job Details

Company Name: Ajanta Pharma Ltd.

Industry: Pharmaceutical Manufacturing

Facility: US FDA Approved Formulation Plant

Job Location: Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra

Employment Type: Full-Time

Application Mode: Email

Last Date to Apply: 15 August 2026

Available Departments

1. EHS (Environment, Health & Safety)

Designation

Executive

Senior Executive

Qualification

B.Sc.

M.Sc.

B.E.

ADIS Certification

Experience

8–10 Years

Key Responsibilities

EHS Compliance

HIRA/JSA

Risk Assessment

Incident Investigation

RCA & CAPA

Fire & Emergency Safety

Environmental Compliance

Work Permit System

EHS Audits

2. PPIC (Production Planning & Inventory Control)

Designation

Executive

Senior Executive

Qualification

B.Pharm

M.Pharm

Experience

8–10 Years

Key Responsibilities

Production Planning

Scheduling

Material Planning

Inventory Control

OSD Manufacturing Experience Preferred

cGMP Compliance

PAS-X Knowledge

Advanced Excel

Cross-functional coordination with Production, QA, QC, Warehouse & Procurement teams

3. IT Department

Designation

Officer

Senior Officer

Qualification

BCA

B.Sc. (Computer Science/IT)

Experience

2–3 Years

Key Responsibilities

IT Support

Hardware & Networking

Pharma Application Support

System Security

Troubleshooting

Knowledge of GMP

Data Integrity

21 CFR Part 11 (Preferred)

Eligibility Criteria

Candidates should possess:

Relevant educational qualification for the applied department.

Required years of pharmaceutical industry experience.

Good communication and analytical skills.

Knowledge of cGMP and regulatory requirements (where applicable).

Ability to work in a cross-functional manufacturing environment.

Selection Process

The selection process may include:

Resume Screening

Technical Interview

HR Interview

Final Selection

Document Verification

How to Apply

Interested and eligible candidates should send their updated resume via email before the application deadline.

Email ID: cv.ptn@ajantapharma.com

Last Date: 15 August 2026

Job Location

Ajanta Pharma Ltd.

B-4/5/6 MIDC Area,

Paithan,

District: Chhatrapati Sambhajinagar,

Maharashtra – 431148

Why Join Ajanta Pharma?

US FDA-approved manufacturing facility

Excellent career growth opportunities

Professional work environment

Exposure to international regulatory standards

Competitive salary and employee benefits

Opportunity to work with advanced pharmaceutical manufacturing technologies

Technical FAQs

1. What is HIRA/JSA in EHS?

HIRA (Hazard Identification and Risk Assessment) and JSA (Job Safety Analysis) are systematic methods used to identify workplace hazards, evaluate risks, and implement preventive safety measures to reduce accidents.

2. What is PPIC in pharmaceutical manufacturing?

PPIC stands for Production Planning and Inventory Control. It ensures efficient production scheduling, raw material availability, inventory management, and timely product delivery while maintaining cGMP compliance.

3. Why is 21 CFR Part 11 important in pharmaceutical IT?

21 CFR Part 11 is a US FDA regulation governing electronic records and electronic signatures. It ensures data integrity, security, traceability, and regulatory compliance in computerized systems.

4. What is RCA & CAPA in pharmaceutical manufacturing?

RCA (Root Cause Analysis) identifies the underlying cause of deviations or incidents, while CAPA (Corrective and Preventive Action) eliminates existing issues and prevents their recurrence to improve product quality and compliance.

5. Why is cGMP knowledge essential for pharmaceutical professionals?

Current Good Manufacturing Practices (cGMP) ensure medicines are consistently produced and controlled according to quality standards. Compliance helps maintain product safety, efficacy, regulatory approval, and patient confidence.