- Full Time
- Dahej, Gujarat

Website Ajanta Pharma
Table of Contents
ToggleAbout Ajanta Pharma:
Ajanta Pharma is a specialty pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality finished dosage forms. With a commitment to addressing global healthcare needs, we produce a comprehensive range of first-to-market products across specialty therapeutic segments.
We are seeking talented professionals to join our Formulation Facility for multiple roles.
1. Production Department
Production Officer / Senior Officer
- Qualification: B.Pharm / M.Pharm
- Experience: 2 to 8 years
- Job Responsibilities:
- Hands-on experience in OSD Manufacturing Operations, including Granulation, Compression, Pellet Coating, Capsule Filling, and both Primary & Secondary Packing.
- Familiarity with electronic Batch Production Records (e-BPR) and electronic logbooks (e-log) is an added advantage.
Production Associate / Operator
- Qualification: 10th, 12th + ITI / Diploma / D.Pharm
- Experience: 2 to 10 years
- Job Responsibilities:
- Experience in OSD Manufacturing processes such as Granulation, Compression, Pellet Coating, Capsule Filling, and Packaging (Blister Packing, Sachet Filling, Bottle & Bulk Packing).
- Expertise in Cartoning, Labelling, Track & Trace operations.
- Knowledge of e-BPR and e-log preferred.
2. Quality Control Department
Quality Control Officer / Senior Officer
- Qualification: B.Pharm / B.Sc. / M.Sc.
- Experience: 2 to 8 years
- Job Responsibilities:
- Experience in analysis of Solid Oral Dosage Forms (Finished Products, In-process, and Stability samples).
- Hands-on expertise in HPLC, UV Spectrophotometer, and Dissolution Tester.
- Knowledge of Analytical Method Validation/Transfer (Solid Oral), GC, ICPMS, and/or LCMS is a plus.
Job Location
📍 Dahej, Gujarat
Walk-in Interview Details
📅 Date: 23rd March 2025 (Sunday)
⏰ Time: 9:00 AM – 4:00 PM
📍 Venue: The Competent Palace, Chakrata Road, Selaqui Industrial Area, Central Hope Town, Selaqui, Dehradun, Uttarakhand – 248197
Important Information for Candidates
✔️ Candidates must have experience in regulatory documentation (cGMP/GDP) and prior work experience in regulated manufacturing plants.
✔️ Only candidates working in USFDA / MHRA-approved facilities should apply.
✔️ Those who have attended an interview with us in the last six months are not eligible.
✔️ Carry an updated CV, CTC details, three recent salary slips, and educational & employment documents for the interview.
🚀 Unable to attend? Send your CV to: 📧 referral.dhj@ajantapharma.com
Join Ajanta Pharma and take your career to the next level! 🚀
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To apply for this job email your details to referral.dhj@ajantapharma.com