Established during the Swadeshi Movement of India, Biological E. Limited (BE) started during a time when the nation sought access to critical healthcare products. Founded and led by Dr. DVK Raju, Biological E. Limited commenced its operations in 1953 as a biological products company manufacturing liver extracts and anti-coagulants. With an objective of transitioning from treating diseases to preventing them, Biological E. Limited launched its Biotechnology Division (now Vaccines and Biologics Division) and commenced large-scale production of DPT vaccines as early as 1962.
Biological E. limited (BE) invites experienced, dynamic and self-motivated candidates with 2 to 10 years of experience for the below positions at its Vaccine Business, Shamirpet Hyderabad
Production - Bulk Manufacturing (Drug Substance / Antigens)
Designation : Assistant Manager / Sr. Executive / Executive / Sr. Officer /Officer
Qualification : MSc (life Science) / B. Pharmacy / Diploma / B. Sc / ITI
Desired Experience : Applicants with relevant experience in vaccine, biosimilars, or injectable manufacturing will be considered a Execute both upstream and downstream activities for bacterial or viral antigens a Execution of production batches for both upstream and downstream. Make sure to execute the process in a timely manner to meet cGMP compliance and batch timelines a Execution of documentation activities for liaison with QA and QC in accordance with cGMP compliance
Production Formulations (Injectables)
Designation : Sr. Executive / Executive / Sr. Officer / Officer
Qualification : Msc (Life science) / B. Pharmacy / Diploma / B. Sc / ITI
Desired Experience :
BLENDING : Able to handle shift plans for formulation activities. Operate and maintain equipment such as autoclaves and blending vessels. Ability to handle and maintain equipment such as autoclaves, blending vessels. CIP and SIP skids a FILLING: Ability to manage shift plans for filling activities. Operate and maintain equipment such as a vacuum cleaner, tunnel steriizer, filling, and capping a PACKING & LABELLING: Ability to handle shift plans for Vial labeling machines and WM dot machines with an inspection system. Managing the Videojet and Control print Printer for batch coding. Operation of Track & Trace System, monitoring of temperature in the told room and deep freezers
Quality Control (Biologics / Vaccines)
Designation : Asst. Manager / Sr. Executive / Executive
Qualification : M.Sc (Life science) /B.Tech/M. Tech (Biotechnology)
Desired Experience :
BIOCHEMICAL ASSAYS : Responsible for estimating the total and free components in polyacrylamide, and conducting biochemical analyses such as protein, nucleic acid, aluminium content, and composition analysis. Experience in verifying analytical methods, adhering to ALCOA principles, and handling 00S and 00T investigations
INSTRUMENTATION TESTING : Expenence in handling analytical instruments such as HPLC and 1C, as well as performing instrument-based assays including molecular size, aggregates, punty, and composition analysis. Basic troubleshooting, 21CFR Part 11, audit trial review practices, ALCOA principles, 00S, 00T systems, and investigations
VIROLOGY : Experience in in-vitro viral testing of starting materials, raw materials, in-process samples, final bulk samples, final lots, and stability samples for viral vaccines. Examine the testing for QC release of products, RM/stability studies of Viral Vaccines, and New projects/Products
QA - IN PROCESS
Designation : Deputy Manager /Asst. Manager /Sr. Executive/ Executive
Qualification : M. Pharmacy /M.Sc/B. Pharmacy
Desired Experience : DRUG SUBSTANCE: Perform IPQA tasks for Bulk Viral Antigen production, which involve maintaining GMP com pliance on the shop floor, clearing lines, dispense and preparing materials Review and approve batch records, SOPs, PV, CV, and APS documents; manage QMS; trend and release batch activities; control and reconcile Master and Working Cell Banks
DRUG PRODUCT : Execute the Fill-finish activities for IPQA. including reviewing SOPs, batch records, executed validations* media fills, line clearance for formulation and filling operations, as well as managing change controls, deviations, 00S investigations, and trend analysis
QMS: Supervising QMS operations, which involve change control, deviations, 00S, 001, CAPA, and self-inspection. 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.
If you're unable to walk-in, you can send your CV to careers@biologicale.com with the subject 'Applying for Department Name'.
PS : If you have already had an interview or been offered a job with us in the past 6 months, please refrain from sharing your profile.
Interested candidates may walk-in with an updated CV, the latest increment letter, and the last 3 months' payslips on Saturday, June 14,2025 from 09:00 a.m. to 02:30 p.m. at
Elite Hotel,
NH 44, Hyderabad, Bangalore Highway,
Macharam, Jadcherla, Telangana.
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