Cronus Pharma Specialities India Pvt. Ltd. is conducting a Walk-in Drive on 29 August 2026 for experienced professionals across Production (OSD), Quality Control (QC), and Injectables functions. The company is looking for candidates with 2–6 years of relevant pharmaceutical experience, with openings covering granulation, blending, compression, analytical QC, injectable QA validation, and IPQA. Candidates with qualifications including ITI, Diploma, B.Sc., B.Pharm, M.Pharm and M.Sc. in Chemistry can apply depending on the role.
📅 Walk-in Interview Details
- Date: 29 August 2026, Saturday
- Time: 9:30 AM – 12:30 PM
- Company: Cronus Pharma Specialities India Pvt. Ltd.
- Venue: Sy. No. 99/11, GMR Hyderabad Aviation SEZ,
Mamidipally Village, Shamshabad, Ranga Reddy, Telangana – 500108 - Contact Person: Ms. Suchitra
- Contact: 7337445157
💼 Open Positions
| Department | Qualification | Experience |
|---|---|---|
| Production – OSD | ITI / Diploma / B.Sc. | 2–4 Years |
| Quality Control (QC) | B.Pharm / M.Pharm / M.Sc. Chemistry | 2–6 Years |
| QA Validation – Injectables | B.Pharm / M.Pharm / M.Sc. Chemistry | 2–6 Years |
| IPQA – Injectables | B.Pharm / M.Pharm / M.Sc. Chemistry | 2–6 Years |
🏭 Production – OSD
Area: Granulation, blending and compression machine operation.
Key responsibilities:
- Operate and monitor granulation, blending and compression machines
- Ensure optimal machine performance and adherence to batch manufacturing records
- Perform line clearance, equipment cleaning and changeover activities
- Follow cGMP guidelines and SOPs
- Troubleshoot machine issues and support process improvement
🔬 Quality Control – QC
Candidates should have hands-on experience with:
- HPLC
- Dissolution
- IR
- Other analytical instruments
Responsibilities:
- Analysis of raw materials, in-process samples and finished products
- Follow pharmacopoeial guidelines
- Maintain accuracy of results
- Instrument maintenance and performance validation
- Ensure laboratory compliance with cGMP and data-integrity requirements
💉 QA Validation – Injectables
Experience in qualification and validation of injectable manufacturing facilities, including:
- Vial washing
- Tunnel
- Filling
- Sealing
- Autoclave
- Vessels
- Area qualification
Additional responsibilities include:
- Execute DQ, IQ, OQ, PQ and PV as per validation protocols
- Prepare and review validation documents and reports
- Ensure compliance with regulatory and cGMP requirements
🧪 IPQA – Injectables
Key responsibilities:
- Conduct in-process quality checks at various stages of injectable manufacturing
- Ensure adherence to SOP, BMR/BPR and cGMP guidelines
- Monitor and review critical process parameters and documentation
- Coordinate with Production and QA teams for timely issue resolution
🎓 Who Can Apply?
This walk-in is particularly suitable for professionals with experience in:
- OSD manufacturing
- Granulation / blending / compression
- Pharmaceutical QC and analytical testing
- Injectable manufacturing
- QA validation
- IPQA
- GMP-regulated pharmaceutical operations
Candidates should carry an updated CV and relevant educational/experience documents to the interview
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