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

Production – Bulk Manufacturing (Drug Substance / Antigens)
Post : Sr. Executive / Executive / Sr. Officer / Officer
Qualification : M.Sc. (Life Sciences) / B.Pharmacy / Diploma / B.Sc. / ITI
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 for both upstream and downstream operations. 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 / Vaccines)
Post : Sr. Executive / Executive / Sr. Officer / Officer
Qualification : M.Sc. (Life Sciences) / B.Pharmacy / Diploma / B.Sc. / ITI
Experience : BLENDING : Ability to manage shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels, CIP and SIP skids
FILLING: Able 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 WM dot machines with an inspection system. Batch Coding through the use of Video jet and Control Printer. Operation of Track and Trace system, monitoring of cold room and deep freezer temperatures

QA
Designation : Sr. Executive/Executive
Qualification : M.Pharmacy / M.Sc. / B.Pharm
Experience : AQA :
• Review of SOPs related to Quality Control and stability protocols
• Responsible for the investigation and closure of 00L, 00T, and 00S
• Examine the log books of the equipment in QC
• Follow up on the closure of deviations, change controls, and CAAPAs related to the QC area
• Keep track of 00S, 00T, and OOLs and maintain the relevant databases and logbooks
• Review the protocols, RORs, and reports for the analytical method validation/other studies
• Checking the accuracy of Media Fill vials
• Review of EMP, water trends, specifications, and testing standards for materials/products
• Prepare and review the Quality Risk assessment documents

QMS : Overseeing QMS activities, including change control, deviations, 00S, OOT, CAPA, and self-inspections, as well as conducting compliance walkthroughs and Gemba walks. Responsibilities also include trending and reviewing QMS metrics, supporting regulatory inspection management, and managing the Site Master File, gap assessments, and quality risk assessments.
IPQA – DRUG SUBSTANCE : Perform IPQA tasks for the production of Bulk Viral Antigens, which includes ensuring GMP compliance on the shop floor, line clearing, dispensing, and preparation processes. 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
IPQA – DRUG PRODUCT : Execute the Fill-Finish activities for IPQA, including reviewing SOPs, batch records, executed validations, and media fills. Line clearance for formulation and filling operations, as well as managing change controls, deviations, QOS investigations, and trend analysis

ENGINEERING (Biologies / Injectables)
Designation : Sr. Executive / Executive / Sr. Officer / Officer
Qualification : B.Tech. / Diploma
Experience : 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. Review the completion status of breakdowns, calibrations, and PM works. Handle basic troubleshooting for Programmable Logic Controllers (PLCs) and Supervisory Control and Data Acquisition (SCADA)

Interested candidates may walk-in with an updated CV, the latest increment letter, and the last 3 months’ payslips on Saturday & Sunday, July 19 & 20,2025 from 09:00 am to 03:00 pm at The Fern Kesarval Hotel & Spa Kesarval Gardens, Bus Stand, Edapally – Panvel Hwy, Cortalim, Quelossim, Verna, Goa 403710

Please refrain from sharing profiles of candidates who have either participated in an interview with us in the last 6 months or have already been offered a job by our organisation. Candidates who are unable to attend the interview may send their CVs to [email protected]