Bharat Biotech Hiring QC & QA

QC & QA Jobs for Graduates at Bharat Biotech Hyderabad

Bharat Biotech hiring QC & QA professionals with graduation or post graduation for injectable and vaccine manufacturing at Hyderabad Genome Valley.

Bharat Biotech International Limited is conducting a walk-in interview for experienced professionals in Quality Control and Quality Assurance at its world-class vaccine and injectable manufacturing facility in Genome Valley, Hyderabad. This hiring drive is aimed at professionals with strong technical expertise in injectable and vaccine manufacturing who are looking to build long-term careers with one of India’s most respected biotechnology organizations.

Company Overview

Bharat Biotech International Limited is a globally recognized biotechnology company known for its leadership in vaccine research, development, and manufacturing. With innovation-driven facilities and approvals from major global regulatory authorities, Bharat Biotech plays a critical role in advancing public health through safe, effective, and affordable vaccines and biologics. The company’s Genome Valley campus in Hyderabad is a hub for cutting-edge pharmaceutical manufacturing, quality systems, and regulatory excellence.

Job Role & Responsibilities

Quality Control – Chemical

Professionals in Quality Control (Chemical) will be responsible for analytical testing and quality evaluation of raw materials, intermediates, and finished products in injectable and vaccine manufacturing.

Key responsibilities include:

• Raw material and finished product analysis as per approved specifications
• Operation and troubleshooting of HPLC, GC, UV, IR, and dissolution instruments
• Stability sample testing and validation sample analysis
• Handling and documentation of OOS and OOT investigations
• Compliance with GMP, GLP, and data integrity requirements

Quality Control – Virology

The Virology QC role involves advanced testing and analysis related to viral vaccines and biologics.

Key responsibilities include:

• PCR, qPCR, and RT-PCR testing
• Cell culture-based virology assays
• Handling mammalian and viro cell lines
• Viral infectivity assays such as plaque assay, TCID50, and focus assays
• ELISA and immunoassays for viral characterization

Quality Control – Microbiology

Microbiology professionals will support sterility assurance and microbial quality monitoring activities.

Key responsibilities include:

• Sterility testing using membrane filtration and direct inoculation methods
• Bioburden and microbial enumeration testing
• Endotoxin testing using LAL/BET methods (gel clot, kinetic, chromogenic)
• Media preparation, qualification, and growth promotion testing
• Environmental monitoring and microbiological documentation

Quality Assurance – QMS

Quality Assurance professionals in QMS will oversee compliance and quality system activities across manufacturing operations.

Key responsibilities include:

• Handling deviations, OOS, OOT, and CAPA
• Change control management and risk assessments
• Annual Product Quality Review (APQR) activities
• Ensuring compliance with regulatory guidelines and internal SOPs

Quality Assurance – QAO / IPQA

This role focuses on on-floor quality assurance and documentation compliance.

Key responsibilities include:

• GMP documentation and data integrity compliance
• Line clearance and in-process quality checks
• Review of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
• Sterility assurance activities and audit support

Quality Assurance – Validation & Qualification

Validation professionals will support equipment, process, and utility qualification.

Key responsibilities include:

• Process validation and cleaning validation activities
• Equipment and utility qualification
• Preparation and review of validation protocols and reports
• Regulatory compliance support during audits

Eligibility / Qualifications

• Qualification: Graduation or Post Graduation
• Relevant degrees include B.Sc, M.Sc, B.Pharm, M.Pharm, and related life sciences disciplines
• Experience: 2 to 12 years of experience in injectable and vaccine manufacturing
• Willingness to work in shifts is mandatory

Relevant courses include: B.Sc Chemistry, B.Sc Microbiology, M.Sc Microbiology, B.Pharm, M.Pharm, M.Sc Biotechnology, M.Sc Virology, Pharmaceutical Sciences, Life Sciences

Location & Work Environment

• Job Location: Genome Valley, Shamirpet, Hyderabad
• Facility Type: Injectable and vaccine manufacturing unit
• Work Schedule: Shift-based operations

Walk-in Interview Details

• Date: 07 February 2026 (Saturday)
• Time: 10:00 AM to 03:00 PM
• Venue: Bharat Biotech International Limited, Genome Valley, Turkapally, Shamirpet, Hyderabad

Documents to Carry

• Updated resume (hard copy)
• Soft copy of resume (PDF or Word) for online registration
• ID Proof (Aadhaar Card and PAN Card)

Application Process

Eligible and interested candidates can attend the walk-in interview directly at the venue on the scheduled date and time. Candidates are advised to carry all required documents and arrive early for registration.

Why Join Bharat Biotech?

• Opportunity to work with a globally respected vaccine manufacturer
• Exposure to advanced injectable and vaccine technologies
• Strong focus on quality, compliance, and innovation
• Long-term career growth in regulated pharmaceutical manufacturing

Frequently Asked Questions (FAQs)

Who can attend this walk-in interview?
Experienced professionals with 2–12 years of experience in injectable or vaccine manufacturing in QC or QA roles.

Are freshers eligible for this drive?
No. This hiring drive is strictly for experienced professionals only.

Is shift work mandatory?
Yes. Candidates must be willing to work in rotational shifts.

Do I need prior vaccine manufacturing experience?
Yes. Experience in injectable and vaccine manufacturing is required.

Can I apply without attending the walk-in?
This recruitment is primarily through walk-in interview. Candidates are encouraged to attend in person.

Company	Bharat Biotech International Limited
Vacancies	Quality Control – Chemical, Virology, Microbiology; Quality Assurance – QMS, QAO/IPQA, Validation
Required Education	Graduation / Post Graduation (B.Sc, M.Sc, B.Pharm, M.Pharm)
Experience	2–12 Years in Injectable & Vaccine Manufacturing