- 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
π Dahej, Gujarat
Walk-in Interview Details
π
Date: 23rd March 2025 (Sunday)
β° Time: 9:00 AM β 4:00 PM
π Venue: The Competent Palace, Chakrata Road, Selaqui Industrial Area, Central Hope Town, Selaqui, Dehradun, Uttarakhand β 248197
Important Information for Candidates
βοΈ Candidates must have experience in regulatory documentation (cGMP/GDP) and prior work experience in regulated manufacturing plants.
βοΈ Only candidates working in USFDA / MHRA-approved facilities should apply.
βοΈ Those who have attended an interview with us in the last six months are not eligible.
βοΈ Carry an updated CV, CTC details, three recent salary slips, and educational & employment documents for the interview.
π Unable to attend? Send your CV to: π§ referral.dhj@ajantapharma.com
Join Ajanta Pharma and take your career to the next level! π
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To apply for this job email your details to referral.dhj@ajantapharma.com
