Ajanta Pharma Walk-In Interview 2026 – Multiple Pharma Jobs
Looking for an experienced pharmaceutical manufacturing or quality assurance job?
Ajanta Pharma Limited is conducting a walk-in interview on 6 September 2026 for several positions connected with its Guwahati manufacturing operations.
The recruitment drive covers Quality Assurance, IPQA, Oral Solid Dosage (OSD) Manufacturing, OSD Packing, Liquid Dosage Manufacturing and Manufacturing/Packing Associate roles.
Candidates with experience ranging from 1 to 10 years, depending on the position, can explore these opportunities.
Important: The interview venue is in Baddi, Himachal Pradesh, while the stated work location is Guwahati, Assam. Candidates should confirm the final posting location with HR before attending.
Ajanta Pharma Recruitment 2026 – Job Overview
| Details | Information |
|---|---|
| Company | Ajanta Pharma Limited |
| Hiring Areas | QA, IPQA, Manufacturing & Packing |
| Experience | 1–10 Years, role dependent |
| Location | Guwahati, Assam |
| Interview Venue | Lemon Tree Hotel, Baddi |
| Interview Date | 6 September 2026 |
| Interview Time | 9:00 AM – 5:00 PM |
| Mode | Walk-In Interview |
| Preferred Candidates | Assam residents preferred |
About Ajanta Pharma
Ajanta Pharma Limited is an Indian pharmaceutical company involved in the development, manufacturing and marketing of finished dosage products.
The company operates across multiple therapeutic segments and markets, with manufacturing operations that require strong systems for quality, documentation, production control and regulatory compliance.
For experienced professionals, these openings offer opportunities to work across different areas of pharmaceutical manufacturing and quality operations.
Ajanta Pharma Job Openings
1. Officer / Senior Officer – Quality Assurance (Lab QA)
Qualification: B.Pharm / M.Pharm
Experience: 2–8 Years
Key Responsibilities
The Lab QA professional will be involved in laboratory quality oversight, including:
- Verification of QC instruments and usage logbooks
- Electronic data reconciliation
- Audit trail verification
- Online review of analytical reports
- Review of laboratory logbooks
- Test plan review and approval through LIMS
- Monitoring QC laboratory activities
- Handling laboratory deviations
- OOS and OOT investigation support
- Root cause analysis
- Quality documentation and compliance
Candidates should have a good understanding of QC laboratory systems, data integrity and pharmaceutical quality practices.
2. Officer / Senior Officer – IPQA (OSD)
Qualification: B.Pharm / M.Pharm
Experience: 2–8 Years
This role focuses on in-process quality assurance for Oral Solid Dosage manufacturing and packing operations.
Key Responsibilities
- Perform line clearance activities
- Monitor dispensing and manufacturing operations
- Conduct IPQA checks in warehouse and production areas
- Monitor packaging activities
- Review BMR and BPR documentation
- Review labels and logbooks
- Check SOP and cGMP compliance on the shop floor
- Support process validation activities
- Conduct hold-time studies according to approved protocols
- Identify and report quality-related observations
Experience with OSD manufacturing and IPQA operations will be useful for this position.
3. Officer / Senior Officer – OSD Manufacturing
Qualification: B.Pharm
Experience: 3–7 Years
Candidates with practical experience in tablet and capsule manufacturing can apply.
Preferred Manufacturing Experience
- Granulation
- Compression
- Coating
- Capsule filling
- eBMR/eBPR systems
- eLog systems
- SAP
- QMS
- TRIMS
- 21 CFR-compliant equipment
Experience with paperless manufacturing systems can be an added advantage.
4. Officer / Senior Officer – OSD Packing
Qualification: B.Pharm / B.Sc
Experience: 3–7 Years
The position involves primary and secondary pharmaceutical packing operations.
Key Skills
- Primary packing
- Secondary packing
- eBPR
- eLog
- Packaging documentation
- 21 CFR-compliant machinery
- Production and quality coordination
Candidates with hands-on experience in pharmaceutical packaging operations can consider this opening.
5. Associate – OSD Manufacturing & Packing
Qualification: 10th / 12th / ITI
Experience: 4–10 Years
This opening is suitable for experienced operators and technicians who have worked with OSD manufacturing or packing equipment.
Equipment Experience
Candidates with experience in equipment such as the following may be considered:
- Glatt
- ACG
- Fette
- Sejong
- IMA-PG
- BQS
- 230 XTS
- Satellite Strip Machine
- A300 Cartonator
- Track & Trace systems
Experience with 21 CFR-compliant machinery is also preferred.
6. Officer / Senior Officer / Executive – Liquid Dosage Manufacturing
Qualification: B.Pharm
Experience: 1–9 Years
Candidates with experience in liquid dosage manufacturing and filling operations can apply.
Relevant Experience
- Liquid dosage manufacturing
- Filling operations
- Sachet filling equipment
- Manufacturing documentation
- Process monitoring
- 21 CFR-compliant machinery
7. Associate – Liquid Dosage Manufacturing & Filling
Qualification: 10th / 12th / ITI
Experience: 4–10 Years
This position is intended for experienced operators familiar with liquid manufacturing and filling equipment.
Preferred Equipment Knowledge
- Manufacturing tanks
- Colloidal mills
- Filling machines
- Sachet filling systems
- Process equipment
- 21 CFR-compliant machinery
Who Can Apply?
The recruitment drive is suitable for candidates with backgrounds in:
- B.Pharm
- M.Pharm
- B.Sc
- ITI
- 10th / 12th with relevant industrial experience
Experience requirements vary significantly by position, from 1 year to 10 years.
Important Preference
Residents of Assam will be given preference for the Guwahati manufacturing requirement.
However, candidates from outside Assam may also consider attending if their profile matches the requirements.
Important Skills & Experience
Depending on the position, candidates should have experience with:
- cGMP
- IPQA
- Quality Assurance
- QC laboratory operations
- OSD manufacturing
- Tablet compression
- Granulation
- Coating
- Capsule filling
- Pharmaceutical packaging
- Liquid dosage manufacturing
- Filling operations
- eBMR / eBPR
- eLog
- SAP / QMS
- LIMS
- 21 CFR-compliant systems
- Deviation and OOS investigations
- Data integrity
- Process validation
- Hold-time studies
Ajanta Pharma Walk-In Interview Details
Date
6 September 2026 (Sunday)
Time
9:00 AM to 5:00 PM
Interview Venue
Lemon Tree Hotel
Baddi-Nalagarh Highway
Baddi, Himachal Pradesh
Work Location
Guwahati, Assam
Candidates should verify the final job location and department with the recruitment team before accepting an offer.
Documents to Carry
Candidates attending the walk-in should carry:
- Updated resume/CV
- Educational certificates
- Experience documents
- Latest salary information
- Relevant employment documents
- Government-issued ID proof
- Passport-size photographs
Experienced candidates should also keep recent salary slips and current CTC details available if requested during the selection process.
How to Apply
Walk-In Interview
Eligible candidates can attend the interview directly at the stated venue on 6 September 2026.
Email Application
Candidates who cannot attend the walk-in can send their updated CV to:
When emailing, mention the position and department clearly in the subject line.
Important Note for Candidates
The recruitment information states a Baddi interview venue for positions associated with the Guwahati work location.
Before travelling, candidates should confirm:
- Exact position being considered
- Final work location
- Interview eligibility
- Required documents
- Any role-specific requirements
This is especially important for candidates travelling from outside Gujarat/Himachal/Assam.
Why Consider Ajanta Pharma?
For professionals already working in pharmaceutical manufacturing or quality operations, these openings provide opportunities to strengthen experience in:
- OSD manufacturing
- Pharmaceutical packing
- IPQA
- Laboratory QA
- Liquid dosage manufacturing
- Electronic manufacturing documentation
- Regulatory compliance
- 21 CFR-related systems
The variety of positions also makes the drive relevant to candidates at different experience levels.
Interview Preparation Tips
Before attending the interview, revise the areas most relevant to your target position.
For QA/IPQA Candidates
Focus on:
- cGMP
- OOS/OOT
- Deviations
- CAPA
- Root cause analysis
- Audit trails
- Data integrity
- BMR/BPR review
- Process validation
For Production Candidates
Revise:
- Granulation
- Compression
- Coating
- Capsule filling
- Manufacturing documentation
- Equipment operation
- eBMR/eBPR
- GMP practices
For Packing Candidates
Prepare around:
- Primary and secondary packing
- Packaging line clearance
- eBPR/eLog
- Track & Trace
- 21 CFR compliance
- Packaging equipment
Frequently Asked Questions
1. When is the Ajanta Pharma walk-in interview?
The walk-in interview is scheduled for 6 September 2026, from 9:00 AM to 5:00 PM.
2. Where is the interview venue?
The interview will take place at Lemon Tree Hotel, Baddi-Nalagarh Highway, Baddi.
3. Where is the job location?
The stated work location for this recruitment is Guwahati, Assam.
4. What departments are hiring?
Openings include Lab QA, IPQA, OSD Manufacturing, OSD Packing, Liquid Dosage Manufacturing, and Manufacturing/Packing Associate positions.
5. Are freshers eligible?
The listed positions are primarily for candidates with relevant experience. The minimum requirement varies from 1 to 4+ years, depending on the position. Candidates should check the specific role before attending.
6. What qualifications are accepted?
Qualifications include B.Pharm, M.Pharm, B.Sc, ITI, 10th and 12th, depending on the position.
