Biological E. Walk-In (Shamirpet, Hyderabad) – Multiple Quality & Engineering Roles

Biological E. Limited, a leading and globally recognized vaccine and pharmaceutical company, is conducting a Walk-In Interview for experienced and dynamic professionals to join our teams in Quality Assurance, Quality Control (Biologics/Vaccines), and Engineering (Injectables/Biologics). This is an excellent opportunity to be part of a company dedicated to providing innovative healthcare solutions. The walk-in drive will be held in Shamirpet, Hyderabad.

Career Opportunities at Biological E. Limited – Walk-In Drive

Join Biological E. Limited and contribute to our mission of “Biological E: Enabling Life, Celebrating Every Day.” We are seeking motivated individuals with relevant experience in the pharmaceutical and biotech sectors to strengthen our quality and engineering departments. This walk-in interview is your chance to explore exciting career paths with a growing organization.

About Biological E. Limited

Biological E. Limited (BE) is a Hyderabad-based global biopharmaceutical company focused on developing and manufacturing vaccines and therapeutics. With a rich history of contributing to public health, BE is committed to innovation, quality, and making a significant impact on global healthcare.

Walk-In Interview Details

Date

Saturday, April 19, 2025

Time

09:30 AM to 03:00 PM

Venue

Biological E. Limited,
Kirloskar (Lebbegauda), Opp. MTR, Bommasandra Industrial Area,
Bengaluru – 560 099. [**Note:** Please confirm the venue as the image mentions Shamirpet, Hyderabad in the introductory text but Bengaluru in the venue section. Prioritize the information that seems most consistent or recent if further clarification is available.]

Open Positions & Requirements

1. Quality Assurance (Designation: Dy. Manager/Asst. Manager/Sr. Executive)

**Qualification:** B. Pharmacy / M. Pharmacy / M. Sc. (Life Science) / B. Tech (Biotechnology)
**Job Roles:**
- **QA – In Process Drug Substance:** Ensure bulk viral antigen production adheres to GMP standards, including line clearance, dispensing, and preparation processes. Examine and approve batch records, standard operating procedures (SOPs), project plans, customer verification (CV), and APS documents. Manage the requirements of trends and batch releases, as well as the control and reconciliation of Master and Working Cell Banks.
- **Drug Product:** Perform IPQA/Fill-Finish tasks, which involve reviewing SOPs, batch records, executed validations, and media fills. Clearing lines for formulation, filling operations, and managing change controls, deviations, OOS investigations, and trend analysis.
- **QMS:** Handle various QMS operations, including changes, deviations, OOS, OOT, 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.
- **Training:** Responsible for preparing, reviewing, and revising employee training processes to ensure that best practices are consistently updated and implemented. Skilled in speaking, reading, and writing Telugu and English, and capable of conducting training sessions in Telugu. Responsible for providing the first GMP training for new recruits, including both technical and casual staff.

2. Quality Control (Biologics/Vaccines) (Designation: Asst. Manager/Sr. Executive)

**Qualification:** M. Sc. (Life Science) / B. Tech (Biotechnology)
**Job Roles:**
- **Biochemical Assays:** Involved in estimating the total and free components of polysaccharides, along with biochemical analyses such as protein, nucleic acid, aluminum content, and composition analysis. Experience in validating analytical methods, adhering to ALCOA principles, and managing OOS and OOT investigations.
- **Instrumentation Testing:** Experience in handling analytical instruments such as HPLC and IC, as well as performing instrument-based assays including molecular size, aggregates, purity, and composition analysis. Basic troubleshooting, 21 CFR Part 11, audit trail review practices, ALCOA principles, OOS, OOT 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. Evaluate testing for the QC release of products, RM/Stability studies of Viral Vaccines, and new projects/products.

3. Engineering (Injectables/Biologics) (Designation: Sr. Executive/Executive/Officer/Jr. Officer)

**Qualification:** B. Tech / Diploma (Mechanical / Instrumentation / Fitter)
**Required Skills:**
- **Instrumentation Maintenance:** Experience in BMS, Breakdown Maintenance, Preventive Maintenance, Calibration, SCADA, PLC.
- **Process Equipment Maintenance:** Experience in handling breakdowns and preventive maintenance of Vial Washing, Filling, Capping, Autoclave and Labelling Machines, Jacketed Vessels, Lyophilization, and ability to handle shift operations.

How to Apply

Interested and eligible candidates are requested to walk-in to the venue on the specified date and time with their updated resume, latest increment letter, and payslips for the last 3 months. Please also carry all relevant original documents for verification.

**Note:** Candidates who have already attended the interview in the past 6 months are requested not to attend again.

Candidates unable to attend the interview may send their CVs to [email protected].