About Company:
Biological E. Limited (BE), the first private sector biological products company in India and the first pharmaceuticals company in South India was established in 1953. Originally incorporated as Biological Products Private Limited, and launched by Dr. Vijay Kumar Datla, today, BE is a globally recognised vaccine manufacturer and has supplied over 2 Billion Doses of Vaccines till date all over the world. BE supplies several essential and lifesaving Vaccines and Pharmaceuticals to UN Agencies viz. UNICEF, PAHO, many global markets, and in India to the National Immunization Program, various State Governments, PSUs, Indian Armed Forces and the domestic retail market. With a mission to improve health and survival of people and contribute to the societies BE serves by providing equitable access to quality vaccines and therapeutics. BE has a long and richly textured history of supporting public health programs in India for over five decades. Our portfolio of WHO pre-qualified vaccines include the 5-in-1 Pentavalent and a Japanese Encephalitis vaccine and our future offerings promise to be even more exciting.
Vacancy Details:
Job Description:
WALK-IN INTERVIEW
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:
1.PRODUCTION-BULK MANUFACTURING(Drug Substance/Antigens)
Designation: 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
2.Perform upstream and downstream activities for bacterial or viral antigens
3.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
4.Execution of documentation activities in liaison with QA and QC in compliance with cGMP regulations
2.PRODUCTION FORMULATIONS(Injectables/Vaccines)
Designation: 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 VVM dot machines with an inspection system. Batch Coding through the use of Videojet and Control Printer. Operation of Track and Trace system, monitoring of cold room and deep freezer temperatures
3.ENGINEERING (Biologics/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)
4.QA:
Designation : Sr. Executive/Executive
Qualification: M.Pharmacy / M.Sc./B. Pharmacy
Experience: AQA:
1.Review of SOPs related to Quality Control and stability protocols
2.Responsible for the investigation and closure of OOL, OOT, and 005
3.Examine the log books of the equipment in QC
4.Follow up on the closure of deviations, change controls, and CAAPAS related to the QC area
5.Keep track of OOS, OOT, and OOLS and maintain the relevant databases and logbooks
6.Review the protocols, RORs, and reports for the analytical method validation/other studies
7.Checking the accuracy of Media Fill vials
8.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 IPOA 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, OOS investigations, and trend analysis
How to Apply?
Walk-in Details:
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
PS: 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 Careers@Biologicale.com
