Walk In Interviews- Bangalore

Biological E. Limited invites experienced, dynamic and self-motivated candidates with 2 to 8 years of experience for the below positions at its Vaccine Business, Shamirpet, Hyderabad:

Designation:

Qualification:

PRODUCTION BULK MANUFACTURING (DRUG SUBSTANCE / ANTIGENS)

Desired Experience: Applicants with relevant experience in vaccine, biosimilars, or injectable manufacturing will be considered.

• Perform upstream and downstream activities for bacterial or viral antigens.
• Execution of production batches in both upstream and downstream areas. Focus on timely execution to ensure that the process is carried out according to cGMP compliance and batch timelines.
• Execution of documentation activities in liaison with QA and QC in compliance with cGMP regulations.

PRODUCTION FORMULATIONS (INJECTABLES)

BLENDING:

Ability to manage shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels, CIP and SIP skids

FILLING:

Ability to manage shift plans for filling activities. Operate and maintain equipment such as a vacuum cleaner, tunnel sterilizer, filling, and capping

PACKING & LABELLING:

Ability to handle shift plans for Vial labeling machines and VVM dot machines with an inspection system. Using the Videojet and Control print Printer for Batch Coding. Operation of Track & Trace System, monitoring of temperature in the cold room and deep freezers.

ENGINEERING (BIOLOGICS/INJECTABLES):

Process Equipment:

Experience in breakdowns and preventive maintenance of Vial Washing, Filling, Capping, Autoclave and Labelling Machines, Jacketed Vessels, lyophilization, and ability to handle shift operations.

Instrumentation:

Ability to handle shift operations for Instrumentation activities such as BMS, Breakdown maintenance, Preventive Maintenance, Calibration, AMC, and interim projects. Reviewing the completion of breakdown status, calibration, and PM works. Handling basic troubleshooting in PLC (Programmable Logic Controllers) and SCADA (Supervisory Control & Data Acquisition).

QUALITY CONTROL (BIOLOGICS / VACCINES):

Biochemical Assays & Immunochemical:

Involved in the estimation of total and free components in polysaccharides, along with biochemical analyses such as protein, nucleic acid, aluminium content, and composition analysis. Experience in analytical method validation, adherence to ALCOA principles, and management of OOS and OOT investigations. Molecular techniques such as SDS: PAGE, Western Blot, Slot blot, PCR and ELISA is preferred.

Virology:

Experience in in-vitro viral testing of starting materials, raw materials, in-process, final bulk, final lot, and stability samples for viral vaccines. Review testing for the QC release of products, RM, stability studies of viral vaccines, and new projects/products.

QA

IPQA

• Ensure that Bulk Viral Antigen production adheres to GMP on the shop floor, line clearance, dispensing, and preparation processes are executed as part of IPQA activities. Reviewing and approving batch records, SOPs, PV, CV, and APS documents; managing QMS; trending and batch release activities; controlling and reconciling Master and Working Cell Banks.
• Perform fill-and-finish tasks for IPQA, which include reviewing SOPs, batch records, executed validations, and media fills, as well as managing change controls, deviations, OOS investigations, and trend analysis.

Sunday, Oct 12, 2025