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!
Job Details:
- 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.