Ajanta Pharma Limited has announced a Walk-In Interview in Vapi, Gujarat, for experienced pharmaceutical professionals. The recruitment drive is being conducted for its US FDA-approved OSD formulation manufacturing facility located at Paithan, District Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.

Candidates with relevant experience in Production, Maintenance, and Quality Assurance departments can attend the walk-in interview. Professionals having experience in regulated pharmaceutical manufacturing facilities and knowledge of cGMP, GDP, QMS, SCADA, PAS-X, equipment qualification, CAPA, deviations, and other regulatory systems will be preferred.

Ajanta Pharma Walk-In Interview – Overview

Particulars Details

Company Name

Ajanta Pharma Limited

Industry

Pharmaceutical Industry

Facility

US FDA Approved OSD Formulation Facility

Departments

Production, Maintenance & Quality Assurance

Positions

Officer / Senior Officer

Experience Required

1 to 8 Years, depending on the position

Job Location

Paithan, Chhatrapati Sambhajinagar, Maharashtra

Walk-In Location

Vapi, Gujarat

Walk-In Date

Sunday, 12 July 2026

Interview Time

10:00 AM to 4:00 PM

Selection Mode

Walk-In Interview

About Ajanta Pharma Limited

Ajanta Pharma Limited is a specialty pharmaceutical company engaged in the development, manufacturing, and marketing of quality finished dosage formulations for domestic and international markets.

The company operates seven state-of-the-art manufacturing facilities in India. This recruitment drive offers experienced pharmaceutical professionals an opportunity to work at Ajanta Pharma’s US FDA-approved Oral Solid Dosage (OSD) formulation facility at Paithan, Maharashtra.

Ajanta Pharma Vacancy Details

Production Department

Position: Officer / Senior Officer

Qualification: B.Pharm / M.Pharm

Experience: 1 to 3 Years and 4 to 8 Years, depending on the job responsibilities.

Candidates with 1 to 3 years of experience should have exposure to OSD manufacturing operations such as granulation, compression, coating, pellet coating, and capsule filling.

Knowledge of PAS-X, SCADA, and Electronic Logbooks (E-Log) is preferred.

Candidates having experience in primary and secondary pharmaceutical packing operations should possess knowledge of PAS-X, E-Log, Track and Trace systems, and Electronic Batch Manufacturing Records (e-BMR).

Candidates with 4 to 8 years of experience should have experience in OSD manufacturing QMS, employee training activities, and equipment qualification.

Knowledge of PAS-X, QMS, and TRIMS is desirable.

Professionals involved in production planning and inventory control should be proficient in Advanced Microsoft Excel, PowerPoint presentations, Power BI, and related AI tools.

Maintenance Department

Position: Officer / Senior Officer

Qualification: BE / DEE in Electrical or Mechanical Engineering

Experience: 4 to 8 Years

Candidates should have practical experience in mechanical or electrical preventive maintenance and breakdown maintenance of pharmaceutical process equipment.

Applicants should possess knowledge of:

PLC and SCADA systems

Electrical panels

Electronic Logbooks

Process equipment maintenance

Software-related breakdown handling

Utility equipment breakdown maintenance

Effluent Treatment Plant (ETP)

Sewage Treatment Plant (STP)

HVAC systems

Humidifiers and dehumidifiers

Air Handling Units (AHU)

Experience in handling software-related breakdowns will be considered an added advantage.

Quality Assurance Department

Position: Officer / Senior Officer

Qualification: B.Pharm / M.Pharm

Experience: 2 to 3 Years and 5 to 6 Years, depending on the job responsibilities.

Candidates with 2 to 3 years of experience should have experience in In-Process Quality Assurance (IPQA) activities related to pharmaceutical manufacturing and packing sections.

Required technical knowledge includes SCADA equipment, PAS-X batch records, equipment qualification, facility qualification, utility qualification, and validation activities.

Candidates with 5 to 6 years of experience should have exposure to Analytical Quality Assurance activities, including:

Analytical report review, online review of chemical and microbiological testing, GLP functions, software qualification of QC instruments, laboratory investigations, and hands-on experience with LIMS, OpenLab, and LC Solution software.

Candidates should also possess working knowledge of pharmaceutical Quality Management Systems and Production Quality Assurance activities, including Change Control, CAPA, Incidents, Deviations, and Market Complaints.

Walk-In Interview Date, Time and Venue

Walk-In Date: Sunday, 12 July 2026

Interview Time: 10:00 AM to 4:00 PM

Venue:

Hotel Woodland

N.H. No. 8, Near Desai Auto Mobiles, Balitha

Vapi, Gujarat – 396191

Documents Required for the Interview

Interested candidates should attend the interview with an updated CV and supporting employment and educational documents.

Candidates are advised to carry their updated CV, current CTC structure, three recent salary slips, educational qualification documents, and previous employment documents.

Important Instructions for Candidates

Candidates applying for all positions should have exposure to regulatory documentation requirements, cGMP and GDP, and preferably experience working in regulated pharmaceutical manufacturing plants.

Interested candidates currently working in US FDA or MHRA-approved facilities are preferred for this recruitment drive.

Candidates should verify their eligibility, experience requirements, interview schedule, and venue details before attending the walk-in interview.

Unable to Attend the Walk-In Interview?

Candidates who are unable to attend the interview can forward their updated CV to:

Email Address: CV.ptn@ajantapharma.com

Applicants should mention the appropriate department and position in the email subject line for better identification of their application.

Why Join Ajanta Pharma?

Ajanta Pharma provides experienced professionals with opportunities to work in regulated pharmaceutical manufacturing operations and gain exposure to advanced systems such as PAS-X, SCADA, e-BMR, QMS, LIMS, Power BI, equipment qualification, validation, and regulatory compliance processes.

Professionals seeking career growth in OSD formulation manufacturing, pharmaceutical engineering, maintenance, and quality assurance can consider this recruitment opportunity.

5 Technical FAQs for Ajanta Pharma Walk-In Interview

1. What are the critical process parameters monitored during OSD granulation and compression?

During granulation, critical parameters include binder addition rate, granulation time, impeller speed, chopper speed, moisture content, and drying temperature. During compression, professionals monitor tablet weight, hardness, thickness, friability, disintegration time, compression force, and machine speed to ensure consistent product quality and compliance with specifications.

2. What is PAS-X, and how is it used in pharmaceutical manufacturing?

PAS-X is a Manufacturing Execution System (MES) widely used in regulated pharmaceutical manufacturing facilities. It supports electronic batch records, production execution, material management, process control, electronic documentation, data integrity, and regulatory compliance while reducing dependence on paper-based manufacturing records.

3. What is the difference between preventive maintenance and breakdown maintenance?

Preventive maintenance is performed according to a predefined schedule to reduce equipment failures and maintain equipment reliability. Breakdown maintenance is performed after equipment failure occurs to restore normal operations. Pharmaceutical maintenance professionals must properly document maintenance activities and assess any potential impact on product quality.

4. What is the role of IPQA in pharmaceutical manufacturing?

IPQA monitors manufacturing and packing activities to ensure compliance with approved procedures, Batch Manufacturing Records, Batch Packing Records, cGMP requirements, and established quality standards. IPQA personnel perform line clearance, in-process checks, sampling, documentation review, deviation reporting, and verification of manufacturing controls.

5. What are CAPA, Change Control, Deviations, and Incidents in pharmaceutical QMS?

CAPA (Corrective and Preventive Action) is used to identify root causes, correct existing problems, and prevent recurrence. Change Control provides a documented system for evaluating and approving proposed changes. A Deviation refers to departure from an approved procedure, specification, or established instruction. An Incident is an unexpected event that may require investigation and assessment of its impact on product quality, patient safety, or regulatory compliance.

Conclusion

The Ajanta Pharma Walk-In Interview 2026 is a valuable opportunity for experienced candidates seeking pharmaceutical jobs in Production, Maintenance, and Quality Assurance departments. Eligible professionals with 1 to 8 years of relevant experience can attend the walk-in interview in Vapi on 12 July 2026.

Candidates should carefully review the eligibility criteria, technical requirements, required documents, and interview venue before attending. Those unable to participate in the walk-in drive can submit their updated CV through the official email address mentioned in the recruitment advertisement.