Ajanta walk-in Warehouse, QC & QA.

Ajanta Pharma Walk In Interview 2026 – B.Pharm, M.Pharm, B.Sc Jobs Pithampur

Ajanta Pharma walk-in interview at Pithampur for B.Pharm, M.Pharm, B.Sc candidates. Multiple Officer vacancies in Warehouse, QC & QA.

Ajanta Pharma Limited is conducting a large-scale walk-in interview drive at its Pithampur (Indore, Madhya Pradesh) manufacturing facility for experienced professionals across Warehouse, Quality Control, and Quality Assurance departments. This hiring initiative targets candidates with hands-on exposure to regulated pharma environments and offers long-term career growth in a globally reputed pharmaceutical organization.

With strong compliance to USFDA and MHRA standards, Ajanta Pharma continues to expand its regulated market operations. These openings are ideal for candidates seeking stable, high-paying pharma jobs with exposure to international regulatory audits, advanced analytical systems, and structured quality systems.

Company Overview

Ajanta Pharma Limited is a leading Indian pharmaceutical company with a strong presence in branded generics across emerging markets and regulated territories. The company operates multiple WHO-GMP compliant manufacturing facilities and has a consistent track record of regulatory approvals from USFDA, MHRA, and other global agencies.

Ajanta is known for its ethical practices, robust R&D pipeline, and employee-centric culture. Working at Ajanta offers direct involvement in high-quality medicine production, compliance-driven operations, and continuous learning in pharmaceutical manufacturing, quality control, and assurance systems.

Job Role & Responsibilities

Warehouse – Officer / Senior Officer (RM Receipt & Dispensing)

Key responsibilities include handling raw material receipt, sampling coordination, and dispensing activities as per SOPs. The role demands strong SAP exposure, inventory control, and documentation accuracy within a regulated manufacturing setup.

Core duties:

• Raw material receipt, verification, and dispensing
• SAP inventory transactions and batch traceability
• Coordination with QC for sampling and release
• Compliance with GDP and GMP requirements
• Documentation as per USFDA and MHRA norms

Quality Control – Officer / Senior Officer

Finished Product / Packing Material QC

• Analysis using HPLC, UV, Dissolution, DT, GC, KF Autotitrator
• Content uniformity, blend uniformity, and finished product testing
• Cleaning validation and hold time study analysis
• LIMS and Chromeleon 7.2 data processing

Stability Section (QC-2)

• Stability sample analysis and trending
• Operation and maintenance of stability chambers
• Regulatory stability data generation
• RS/Assay processing using Chromeleon

Raw Material Section (QC-2)

• Raw material and excipient analysis
• Residual solvent testing and chromatogram review
• Advanced instrument handling: ICP-MS, Malvern PSA, IR

GLP – Quality Control

GLP roles involve independent handling of reference standards, working standards, and impurity standards. Responsibilities also include analytical method transfer, SOP harmonization, stability chamber qualification, and audit-ready documentation.

Microbiology QC roles focus on environmental monitoring, water system analysis, media preparation, and microbiological testing of RM, PM, and finished goods.

Quality Assurance – Lab QA, IPQA & QMS

QA professionals will manage batch record review, line clearance, deviation handling, CAPA closure, and qualification/validation activities.

Key QA responsibilities:

• Online batch review and pre-checks
• In-process quality assurance during manufacturing and packing
• Process, cleaning, and hold time validation
• HVAC qualification and requalification
• APQR preparation and e-logbook implementation
• QMS documentation, audits, and compliance reviews

Eligibility / Qualifications

Required education includes:
B.Pharmacy, M.Pharmacy, B.Sc, M.Sc, D.Pharmacy, B.Com

Relevant specializations:
Pharmaceutical Sciences, Analytical Chemistry, Microbiology, Biotechnology, Life Sciences, Quality Assurance, Quality Control

Experience requirements range from 2 to 12 years depending on role and department. Candidates must have prior exposure to regulated OSD manufacturing environments.

Location & Salary

Location:
Ajanta Pharma Limited
Plot No. 55, 56, 57, ISEZ, Phase II,
Pithampur, Dist. Dhar – 454775
Madhya Pradesh

Salary:
Compensation will be industry-aligned and based on experience, technical expertise, and interview performance. Ajanta Pharma offers competitive CTC packages, performance incentives, and long-term career stability.

Walk-In Interview Details

Quality Control Walk-In

Date: Friday, 30 January 2026
Time: 10:00 AM to 3:00 PM

Warehouse, GLP, Micro & QA Walk-In

Date: Saturday, 31 January 2026
Time: 10:00 AM to 3:00 PM

Venue:
Ajanta Pharma Limited, Pithampur Unit (Address above)

Application Process

This is a direct walk-in interview. Eligible candidates should report to the venue on the scheduled date and time.

Mandatory documents:

• Updated resume
• Current CTC proof / salary slip
• One passport-size photograph

Candidates who appeared for any Ajanta Pharma interview in the last 6 months are not eligible.

Ajanta Pharma does not charge any recruitment fees. Candidates are advised to avoid fraudulent agencies.

Why Join Ajanta Pharma?

• Strong USFDA & MHRA regulatory exposure
• High-paying pharma jobs with long-term stability
• Advanced analytical instruments and digital QMS systems
• Ethical, transparent hiring practices
• Career growth in regulated pharma manufacturing

Frequently Asked Questions (FAQs)

Q1. Is this walk-in open for freshers?
No. These roles require relevant pharma industry experience.

Q2. Is SAP or LIMS experience mandatory?
Yes. Most roles require hands-on experience with SAP, LIMS, or Chromeleon.

Q3. Are candidates from OSD manufacturing eligible?
Yes. OSD manufacturing experience is preferred.

Q4. Is there any application fee?
No. Ajanta Pharma does not charge any fee.

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Ajanta Pharma Walk-In Interview – Vacancy Summary

Company	Ajanta Pharma Limited
Vacancies	Officer / Senior Officer – Warehouse, QC (Finished Product, Stability, Raw Material), GLP QC, Micro QC, Lab QA, IPQA, QMS
Required Education	B.Pharm, M.Pharm, B.Sc, M.Sc, D.Pharm, B.Com
Experience	2 to 12 Years