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Biological E. Limited Announces Walk-In Drive for Pharma Professionals in Hyderabad
In a significant recruitment drive, Biological E. Limited (BE), a leading name in the Indian pharmaceutical industry, has announced a walk-in interview for experienced professionals. The company is seeking to bolster its Speciality Injectables Business unit located at its facility in Shamirpet, Hyderabad.
This initiative aims to attract skilled talent across various critical departments, including Production, Engineering, Quality Control, and Microbiology. The walk-in presents a prime opportunity for qualified candidates to join a company renowned for its commitment to quality and innovation in healthcare.
A Deep Dive into the Open Positions
Biological E. is recruiting for multiple roles with a range of experience levels, from officers to managers. Here’s a detailed breakdown of the available positions:
1. Production (Injectables)
Designations: Officer, Sr. Officer, Executive, Sr. Executive
Qualification: Diploma, B.Sc., M. Pharmacy, B. Pharmacy, or M.Sc.
Experience: 2 to 10 years
Relevant Roles: Expertise in Filling, Autoclave, Compounding, and Lyophilization (Lyo) processes.
2. Engineering
Designations: Officer, Sr. Officer, Executive, Sr. Executive, DM, Manager
Qualification: Diploma or B.Tech.
Experience: 2 to 14 years
Relevant Roles: Process engineering, Instrumentation, Building Management Systems (BMS), Utilities, and HVAC Water systems.
3. Quality Control
Designations: Executive, Sr. Executive, Assistant Manager
Qualification: B. Pharmacy or M.Sc.
Experience: 2 to 6 years
Relevant Roles: Handling Raw Materials, Finished Goods testing, Stability studies, and Investigations under the Quality Management System (QMS).
4. Microbiology
Designations: Executive, Sr. Executive, Assistant Manager
Qualification: M.Sc. in Microbiology or Biotechnology
Experience: 2 to 9 years
Relevant Roles: Microbiology Testing, Environmental Monitoring, and QMS activities.
Walk-In Interview Details
Interested and eligible candidates are invited to attend the walk-in interview with the necessary documents.
Date: Sunday, November 2, 2025
Time: 9:00 AM to 2:00 PM
Venue: Sayaji Hotel, Near Bhimnath Bridge, Opposite Parsi Agyari, Parshuram Nagar, Sayajigani, Vadodara – 390020, India.
Mandatory Documents to Bring
Candidates must carry the following documents for the interview:
· An updated resume.
· The latest increment letter.
· Payslips for the last three months.
Key Eligibility and Instructions
· The company has explicitly stated that only candidates with relevant pharmaceutical experience are eligible to attend.
· Individuals who have been interviewed by Biological E. Limited in the last six months or have previously been offered a position are requested not to attend.
For those who are unable to be present at the walk-in venue but possess the requisite qualifications, the company has provided an alternative: they can email their CVs to Careers@biologicale.com.
About Biological E. Limited
Biological E. Limited is a pioneering pharmaceutical company with a robust portfolio that includes vaccines, injectables, and other therapeutic products. With a legacy of quality and a mission to “celebrate life,” the company has established itself as a trusted and innovative player in the global healthcare landscape. This recruitment drive for its speciality injectables division underscores its continued growth and dedication to strengthening its team with top-tier talent.
FAQ:
1. What are the critical parameters monitored during the Lyophilization (Lyo) process in injectables manufacturing?
Answer:
Key parameters include:
Shelf temperature (for primary and secondary drying stages)
Chamber pressure (vacuum level)
Product temperature (monitored using thermocouples or PAT tools)
Condenser temperature (for vapor trapping efficiency)
Drying time and cycle validation
These parameters ensure consistent moisture removal and product stability in sterile injectables.
2. What are common preventive maintenance (PM) activities for HVAC and BMS systems in sterile manufacturing areas?
Answer:
Regular filter integrity testing (HEPA/ULPA)
Differential pressure calibration across classified areas
Airflow velocity checks in LAFs and RLAFs
Temperature and humidity sensor calibration
Alarm and interlock validation through BMS
These activities ensure consistent cleanroom environmental conditions as per GMP and ISO Class 7/8 standards.
3. How is the sterility of injectable products ensured during the aseptic filling process?
Answer:
Sterility is maintained through:
Use of Grade A (ISO 5) laminar air flow zones
Validated sterilization cycles for components, equipment, and media
Environmental monitoring (viable & non-viable particles)
Media fill simulation to validate aseptic practices
Personnel gowning qualification and aseptic technique training
4. What are the typical tests performed in Quality Control for injectable products?
Answer:
Common QC tests include:
pH determination and assay of active ingredients
Sterility testing (as per pharmacopeial methods)
Particulate matter testing (light obscuration or microscopic method)
Endotoxin testing (LAL test)
Osmolality and clarity check
Stability studies under ICH conditions (real-time and accelerated)
5. What microbiological monitoring practices are followed in sterile manufacturing areas?
Answer:
Microbiology teams typically perform:
Environmental Monitoring (EM): Settle plates, active air sampling, surface swabs, and personnel monitoring
Water system monitoring: Total viable count (TVC) and endotoxin testing for WFI and purified water
Gown and glove fingertip tests for aseptic area personnel
Identification of isolates using biochemical or molecular methods
Trend analysis and CAPA for EM deviations
