Website Ajanta Pharma
About Ajanta Pharma:
Ajanta Pharma, a specialty pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality finished dosage formulations, is looking for skilled professionals to join its Formulation Facility. With a commitment to serving healthcare needs globally, we provide first-to-market products across specialty therapeutic segments.
Walk-in Interview Details
📅 Date: Sunday, February 16, 2025
🕘 Time: 09:00 AM – 04:00 PM
📍 Venue: Hotel Novotel, Iscon Cross Road, Sarkhej – Gandhinagar Highway, next to Wide Angle Cinema, Ahmedabad, Gujarat 380015
Open Positions
Production Department
1. Officer / Senior Officer
- Qualification: B.Pharm / M.Pharm
- Experience: 2 to 8 years
- Key Responsibilities:
- Hands-on experience in OSD (Oral Solid Dosage) Manufacturing operations, including:
- Granulation
- Compression
- Pellet Coating
- Capsule Filling
- Primary & Secondary Packing
- Familiarity with e-BPR and e-log will be an added advantage.
- Hands-on experience in OSD (Oral Solid Dosage) Manufacturing operations, including:
2. Associate / Operator
- Qualification: 10th / 12th + ITI / Diploma / D.Pharm
- Experience: 2 to 10 years
- Key Responsibilities:
- Involvement in OSD Manufacturing processes similar to Officer/Sr. Officer roles.
- Knowledge of cGMP compliance and regulatory documentation preferred.
Quality Control Department
3. Officer / Senior Officer
- Qualification: B.Pharm / B.Sc. / M.Sc.
- Experience: 2 to 8 years
- Key Responsibilities:
- Experience in Solid Oral analysis, including:
- Finished Products (FP)
- In-process & Stability samples
- Hands-on experience with:
- HPLC, UV Spectrophotometer, Dissolution Tester
- Analytical Method Validation/Transfer (Solid Oral)
- GC, ICPMS, LCMS operation
- Experience in Solid Oral analysis, including:
Quality Assurance Department
4. Officer / Senior Officer
- Qualification: B.Pharm / B.Sc. / M.Sc.
- Experience: 2 to 8 years
- Key Responsibilities:
- Expertise in:
- DRA (Drug Regulatory Affairs)
- IPQA (In-Process Quality Assurance)
- Validation & AQA (Analytical Quality Assurance)
- Preference for candidates currently working in USFDA-approved facilities.
- Expertise in:
Job Location
📍 Dahej, Gujarat
Additional Information
✅ Preferred Candidates:
- Experience in regulatory documentation (cGMP / GDP)
- Background in regulated plants with compliance exposure
- Candidates from USFDA/MHRA-approved facilities
✅ Documents Required:
- Updated CV
- Current CTC structure
- Three recent salary slips
- Educational qualification certificates
- Previous employment documents
🚫 Note: Candidates who have attended an interview with Ajanta Pharma in the past six months are not eligible.
📧 Can’t attend the interview? Send your updated CV to resume.dahej@ajantapharma.com
Join Ajanta Pharma and be a part of our commitment to innovation and healthcare excellence!
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To apply for this job email your details to resume.dahej@ajantapharma.com