Ajanta Pharma Walk-in Production Officers

B.Pharm/M.Pharm Production Jobs (3 Roles) – Pithampur

Ajanta Pharma hiring Production Officers in Pithampur. 3 roles. B.Pharm/M.Pharm with 4–10 years OSD experience. Walk-in on 24 Dec 2025.

Ajanta Pharma Limited has announced a dedicated walk-in interview drive for experienced pharmaceutical manufacturing professionals at its Pithampur formulation facility near Indore, Madhya Pradesh. This hiring initiative targets skilled candidates with hands-on exposure to oral solid dosage (OSD) manufacturing, packing operations, and production quality systems within regulated pharmaceutical environments. Professionals seeking long-term careers in formulation manufacturing, production compliance, and regulated plant operations will find this opportunity highly relevant.

The Pithampur plant is a key manufacturing site supporting Ajanta Pharma’s domestic and international product portfolio. The current openings are designed for professionals who can independently handle critical production activities, ensure documentation accuracy, and support compliance with global regulatory standards.

Company Overview

Ajanta Pharma Limited is a leading specialty pharmaceutical company with a strong presence across branded generics, formulations, and regulated markets worldwide. The company operates multiple manufacturing facilities approved by global regulatory authorities such as USFDA, MHRA, and other international agencies.

Known for its consistent quality standards and compliance-driven culture, Ajanta Pharma focuses on producing high-quality medicines across therapeutic segments including cardiology, dermatology, ophthalmology, pain management, and anti-infectives. Working at Ajanta Pharma offers professionals exposure to advanced manufacturing systems, electronic batch records, and globally regulated operations.

Job Role & Responsibilities

Production – Manufacturing Officer / Senior Officer

(Granulation, Blenders, Compression, Coating, Capsule Filling)

• Operate and supervise OSD manufacturing processes including granulation, blending, compression, coating, and capsule filling.
• Handle day-to-day production activities while ensuring adherence to cGMP and SOP requirements.
• Maintain accurate documentation including batch manufacturing records and electronic logbooks.
• Support smooth execution of production plans with minimal deviations.
• Ensure compliance with electronic batch manufacturing records (EBMR) and E-log systems.

Production – Primary & Secondary Packing Officer / Senior Officer

(Primary Packing, Secondary Packing, PM Dispensing)

• Manage primary and secondary packing operations for OSD products.
• Oversee packing material dispensing and reconciliation activities.
• Ensure compliance with packaging SOPs, cGMP, and data integrity requirements.
• Maintain packing documentation, batch records, and electronic logs.
• Coordinate with quality and production teams to meet dispatch timelines.

Production – QMS Executive / Officer / Senior Officer

• Handle production quality management system activities including change control, deviations, and CAPA.
• Prepare, review, and maintain SOPs, training records, and controlled documentation.
• Support internal audits, regulatory inspections, and compliance reviews.
• Ensure documentation accuracy and alignment with USFDA and MHRA regulatory expectations.
• Coordinate training and implementation of QMS processes across production teams.

Eligibility / Qualifications

Required Education

B.Pharmacy, M.Pharmacy

Experience Requirements

• Manufacturing & Packing Roles: 4 to 8 years of relevant OSD formulation experience.
• QMS Role: 5 to 10 years of experience in production QMS within pharmaceutical manufacturing.

Key Experience & Skills

• Mandatory exposure to OSD manufacturing operations.
• Hands-on experience with E-log and EBMR systems.
• Strong understanding of cGMP documentation and regulatory compliance.
• Experience working in USFDA and MHRA regulated manufacturing environments.
• Candidates from OSD or liquid oral manufacturing backgrounds are eligible.

Location & Salary

• Job Location: Pithampur, Indore, Madhya Pradesh
• Salary: Competitive and aligned with industry standards, based on experience and role level.

Walk-In Interview Details

• Date: Wednesday, 24 December 2025
• Time: 10:00 AM to 3:00 PM
• Venue: Ajanta Pharma Limited, Plot No. 55, 56, 57, ISEZ Phase II, Pithampur, District Dhar – 454775

Documents to Carry

• Updated resume
• Current compensation letter
• One passport-size photograph

Important Notes

• Ajanta Pharma does not charge any fee at any stage of recruitment.
• Candidates who have attended an interview at Ajanta Pharma in the last 6 months are not eligible.

Frequently Asked Questions (FAQs)

Who can attend this walk-in interview?
Candidates with B.Pharm or M.Pharm qualifications and relevant OSD manufacturing experience can attend.

Is freshers eligible?
No. This drive is strictly for experienced professionals.

Is regulatory exposure mandatory?
Yes. Experience in USFDA or MHRA regulated environments is required.

Is electronic documentation experience required?
Yes. Exposure to E-log and EBMR systems is mandatory.

Summary Table

Company	Ajanta Pharma Limited
Vacancies	3 Roles (Manufacturing, Packing, QMS)
Required Education	B.Pharm, M.Pharm
Experience	4–10 Years (OSD Manufacturing & QMS)