**Cronus Pharma Specialities India Pvt. Ltd. Walk-in Drive for Experienced Professionals**
Cronus Pharma Specialities India Pvt. Ltd. is conducting a Walk-in Drive for seasoned pharmaceutical professionals. We invite dynamic individuals with 2-6 years of relevant experience to join our growing team across **Production (OSD), Quality Control (QC), QA Validation (Injectables), and IPQA (Injectables)** functions.
**About Cronus Pharma Specialities:**
We are a rapidly growing pharmaceutical company dedicated to delivering high-quality healthcare solutions. Our commitment to innovation and excellence provides a challenging yet rewarding environment for career growth in a cGMP-compliant setting.
**Opportunities Available:**
**1. Production – OSD**
* **Experience:** 2-4 Years
* **Qualification:** ITI / Diploma / B.Sc.
* **Key Responsibilities:** Operate and monitor granulation, blending, and compression machines. Ensure optimal performance, adhere to Batch Manufacturing Records (BMRs), perform line clearance, equipment cleaning, changeover activities, and strictly follow cGMP guidelines and SOPs. Troubleshoot and support process improvements.
**2. Quality Control (QC)**
* **Experience:** 2-6 Years
* **Qualification:** B.Pharm / M.Pharm / M.Sc. Chemistry
* **Key Responsibilities:** Conduct analysis of raw materials, in-process samples, and finished products. Must have hands-on experience with analytical instruments such as HPLC, Dissolution, and IR. Ensure pharmacopoeial guideline adherence, data accuracy, instrument maintenance, and laboratory compliance with cGMP and data integrity.
**3. QA Validation – Injectables**
* **Experience:** 2-6 Years
* **Qualification:** B.Pharm / M.Pharm / M.Sc. Chemistry
* **Key Responsibilities:** Expertise in qualification and validation of injectable manufacturing facilities, including vial washing, tunnel, filling, sealing, autoclave, vessels, and area qualification. Execute DQ, IQ, OQ, PQ, and PV as per protocols. Prepare and review validation documents, ensuring regulatory and cGMP compliance.
**4. IPQA – Injectables**
* **Experience:** 2-6 Years
* **Qualification:** B.Pharm / M.Pharm / M.Sc. Chemistry
* **Key Responsibilities:** Perform in-process quality checks throughout injectable manufacturing. Ensure adherence to SOPs, BMR/BPRs, and cGMP guidelines. Monitor critical process parameters, review documentation, and coordinate with Production and QA for issue resolution.
**General Requirements:**
We are seeking professionals with proven experience in GMP-regulated pharmaceutical operations.
**Walk-in Interview Details:**
* **Date:** Saturday, 29 August 2026
* **Time:** 9:30 AM – 12:30 PM
* **Venue:** Sy. No. 99/11, GMR Hyderabad Aviation SEZ, Mamidipally Village, Shamshabad, Ranga Reddy, Telangana – 500108
* **Contact Person:** Ms. Suchitra
* **Contact Number:** 7337445157
**Don't forget to bring your updated CV and all relevant educational and experience documents.**
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