Exciting Career Opportunities at Biological E. Limited 🚀
Biological E. Limited is on the lookout for experienced, dynamic & self-motivated professionals with 2 to 8 years of experience to join our Vaccine Business at Shamirpet, Hyderabad. If you’re ready to grow and contribute to cutting-edge vaccine manufacturing, this is your chance!
- ✨Positions Offered: Sr. Executive / Executive / Sr. Officer / Officer
- 🎓Qualifications Required: M.Sc. (Life Sciences) / B. Pharmacy / Diploma / B.Sc. / ITI
🧫 Production – Bulk Manufacturing (Drug Substance / Antigens)
- 🔹 Relevant experience in vaccine, biosimilars, or injectable manufacturing
- Perform upstream & downstream processing of bacterial/viral antigens
- 🔹 Execute production batches with strict cGMP compliance & timelines
- 🔹 Coordinate with QA & QC teams for accurate documentation
💉 Production Formulations (Vaccines)
Blending:
🔹 Manage shift plans for formulation activities
🔹 Operate autoclaves, blending vessels, CIP & SIP skids
Filling:
🔹 Manage filling shift plans
🔹 Operate vacuum cleaners, tunnel sterilizers, filling & capping machines
Packing & Labelling:
🔹 Manage vial labeling & VVM dot machines with inspection system
🔹 Operate Videojet & Control Print printers for batch coding
🔹 Handle Track & Trace system and cold room/freezer temperature monitoring

🛠️ Engineering (Biologics)
Process Equipment:
🔹 Breakdown & preventive maintenance of vial washing, filling, capping, autoclave, labeling machines, jacketed vessels, lyophilization
🔹 Efficiently handle shift operations
Instrumentation:
🔹 Shift handling of BMS, breakdown maintenance, calibration, AMC & interim projects
🔹 Troubleshooting in PLC & SCADA systems
🔬 Quality Control (Biologics / Vaccines)
Biochemical & Immunochemical Assays:
Total & free component estimation in polysaccharides, proteins, nucleic acids, aluminum content
🔹 Analytical method validation & ALCOA compliance
🔹 OOS & OOT investigations management
🔹 Molecular techniques (SDS-PAGE, Western Blot, PCR, ELISA)
Virology:
🔹 In-vitro viral testing of raw materials, in-process, bulk & final lots
🔹 Review QC release testing and stability studies
✅ Quality Assurance (IPQA – Drug Substance / Drug Product)
🔹 Ensure GMP compliance on shop floor, line clearance, dispensing & preparation
🔹 Review & approve batch records, SOPs, PV, CV, APS documents
🔹 Manage QMS, trending, batch release activities
🔹 Control & reconcile Master & Working Cell Banks
🔹 Perform fill-&-finish IPQA activities including media fills, validations, change controls, deviations, investigations
Walk-in Interview Details:
🗓️ 12th Oct’25 (Sunday)
⏰ 09:00AM – 02:00PM
📍 Sai Vishram Hotel, Hebbagodi, 144-C/1 Kirloskar Road, Opp. MTR, Bommasandra Industrial Area, Bengaluru, Karnataka
Please bring: Updated CV, latest increment letter, last 3 months pay Slips.
ABAC
