Ajanta Pharma Limited is conducting a Walk-In Interview in Guwahati, Assam, on 13 September 2026 for experienced candidates across Quality Assurance, Manufacturing, Packing, Liquid Dosage and Maintenance departments.
This Ajanta Pharma Guwahati recruitment 2026 drive offers opportunities for candidates with B.Pharm, M.Pharm, B.Sc, Diploma, B.E., ITI, 10th and 12th qualifications, depending on the position. Open designations include Associate, Officer, Senior Officer and Executive.
Ajanta Pharma Limited is a specialty pharmaceutical company engaged in the development, manufacturing and marketing of finished dosage forms for domestic and international markets. The openings are associated with its formulation facility in Guwahati, Assam.
Ajanta Pharma Walk-In Interview 2026 – Overview
| Particular | Details |
|---|---|
| Company | Ajanta Pharma Limited |
| Departments | Quality Assurance, Manufacturing, Packing, Liquid Dosage, Maintenance |
| Positions | Associate, Officer, Sr. Officer, Executive |
| Qualifications | B.Pharm, M.Pharm, B.Sc, Diploma, B.E., ITI, 10th, 12th |
| Experience | Role-dependent, up to 10 years |
| Facility | Guwahati, Assam |
| Walk-In Date | 13 September 2026 (Sunday) |
| Interview Time | 10:00 AM to 5:00 PM |
| Interview Venue | Hotel Hashtag Inn, Lokhra, Guwahati, Assam |
| Resume Email | ghthr@ajantapharma.com |
| Preference | Local candidates from Assam |
1. Quality Assurance – Lab QA
Position: Officer / Senior Officer
Qualification: B.Pharm / M.Pharm
Experience: 2–8 years
Key Responsibilities
Candidates selected for Ajanta Pharma Quality Assurance jobs in Lab QA may be responsible for:
- Verification of QC instruments and instrument usage logbooks.
- Electronic data reconciliation and audit-trail verification for QC instruments.
- Online review of analytical reports and laboratory logbooks.
- Reviewing and approving test plans in LIMS.
- Online review of Quality Control laboratory activities.
- Handling laboratory deviations, OOS and OOT investigations.
- Supporting root-cause investigations and laboratory compliance activities.
Candidates with pharmaceutical QA, data-integrity, LIMS, OOS/OOT and QC laboratory compliance experience will be particularly relevant for this opening.
2. Quality Assurance – IPQA OSD
Position: Officer / Senior Officer
Qualification: B.Pharm / M.Pharm
Experience: 2–8 years
Key Responsibilities
- Perform line clearance for dispensing, manufacturing and packaging activities.
- Conduct in-process checks.
- Perform IPQA activities in warehouse, manufacturing and packaging areas.
- Review BMR, BPR, labels and logbooks online.
- Check SOP and cGMP compliance on the shop floor.
- Carry out process validation and hold-time studies according to approved protocols.
This role is suitable for professionals with hands-on experience in IPQA, oral solid dosage manufacturing, cGMP compliance, validation and pharmaceutical documentation.
3. Manufacturing – Oral Solid Dosage
Position: Officer / Senior Officer
Qualification: B.Pharm
Experience: Experienced candidates; the source notice indicates an upper limit of 7 years.
Key Responsibilities
Applicants should have exposure to OSD manufacturing operations including:
- Granulation
- Compression
- Coating
- Capsule filling
- eBMR/eBPR
- Electronic logs
- SAP
- QMS
- 21 CFR-compliant manufacturing equipment
Candidates with practical experience in regulated pharmaceutical formulation manufacturing will be preferred.
4. Packing – Oral Solid Dosage
Position: Officer / Senior Officer
Qualification: B.Pharm / B.Sc
Experience: 3–7 years
Key Responsibilities
- Primary packing operations.
- Secondary packing operations.
- Handling 21 CFR-compliant equipment.
- Pharmaceutical packing documentation.
- Experience with eBPR and electronic logs will be an added advantage.
5. Manufacturing & Packing – Associate
Position: Associate
Qualification: 10th / 12th / ITI
Experience: 4–10 years
Required Experience
Candidates should have exposure to OSD manufacturing and packing equipment such as:
- Glatt
- ACG
- Fette
- Sejong
- IMA-PG
- BQS
- 230 XTS
- Satellite strip machines
- A300 Cartonator
- Track & Trace systems
Knowledge of handling 21 CFR-compliant pharmaceutical equipment is required.
6. Liquid Dosage (Jelly) – Manufacturing/Filling
Position: Officer / Senior Officer / Executive
Qualification: B.Pharm
Experience: 1–9 years
Key Responsibilities
Candidates should have relevant liquid dosage manufacturing experience, including:
- Liquid manufacturing operations.
- Filling operations.
- Sachet filling machinery.
- Handling of 21 CFR-compliant machines.
- Compliance with regulated pharmaceutical manufacturing practices.
7. Liquid Manufacturing/Filling – Associate
Position: Associate
Qualification: 10th / 12th / ITI
Experience: 1–10 years
Key Responsibilities
Applicants should have knowledge of liquid manufacturing and filling equipment, including:
- Manufacturing tanks.
- Colloidal mills.
- Sachet filling machines.
- Other liquid manufacturing/filling equipment.
- 21 CFR-compliant machinery.
8. Maintenance
Position: Officer
Qualification: Diploma / B.E.
Experience: 2–6 years
Key Responsibilities
The Maintenance Officer position involves responsibilities related to plant machinery and utilities across OSD, sterile and ointment blocks.
Responsibilities include:
- Plant machinery and utility maintenance.
- Preventive and routine maintenance planning.
- Tracking and maintaining critical spare parts.
- Supporting engineering and maintenance projects.
- Maintenance of shop-floor machinery.
- Handling equipment in accordance with 21 CFR requirements.
- Supporting GMP-compliant utility operations.
- Electrical work involving plant HT/LT lines.
Candidates from pharmaceutical or FMCG manufacturing backgrounds are preferred.
Who Can Apply for Ajanta Pharma Jobs?
Candidates may apply based on the qualification specified for each department:
- B.Pharm / M.Pharm: Quality Assurance roles.
- B.Pharm: OSD Manufacturing and Liquid Dosage roles.
- B.Pharm / B.Sc: OSD Packing positions.
- 10th / 12th / ITI: Associate-level Manufacturing, Packing and Liquid Manufacturing/Filling positions.
- Diploma / B.E.: Maintenance Officer role.
Applicants should ensure that their qualification and relevant work experience match the specific Ajanta Pharma vacancy before attending the interview.
Why Consider Ajanta Pharma Recruitment?
The recruitment drive provides candidates an opportunity to work in a regulated pharmaceutical formulation manufacturing environment with exposure to areas such as cGMP, 21 CFR compliance, electronic batch records, QMS, LIMS, IPQA, OSD manufacturing, packing, liquid dosage manufacturing and pharmaceutical engineering.
The recruitment notice also highlights Ajanta Pharma’s Great Place to Work certification for the stated certification period.
Ajanta Pharma Walk-In Interview Date and Venue
Walk-In Date: 13 September 2026 (Sunday)
Time: 10:00 AM to 5:00 PM
Venue: Hotel Hashtag Inn, Lokhra, Guwahati, Assam
Candidates attending the Ajanta Pharma Walk-In Interview in Guwahati should carry:
- Updated resume/CV.
- One passport-size photograph.
- Latest salary slip.
The company has stated that preference will be given to local candidates from Assam.
How to Apply for Ajanta Pharma Guwahati Jobs
Eligible candidates can directly attend the walk-in interview at the specified venue on 13 September 2026 between 10:00 AM and 5:00 PM.
Candidates who are unable to attend the Ajanta Pharma walk-in interview may send their updated resume to:
Email: ghthr@ajantapharma.com
