Dr Reddy’s walk-in QA & QC

Dr Reddy’s Biologics QA QC Hiring Walk-in 2026
Dr Reddy’s Biologics hiring QA & QC Associates. Life Sciences graduates with 3–10 yrs exp. Walk-in Bangalore April 19.

Looking for high-growth biotech and pharmaceutical jobs in Quality Assurance and Quality Control? Dr. Reddy’s Biologics is conducting a career expo with multiple vacancies for QA and QC Associates across specialized domains. This hiring drive is open for experienced professionals with 3 to 10 years of experience in life sciences, offering roles in Analytical QA, Drug Product QA, Microbiology QC, Molecular Biology, Bioassay, and more.

The walk-in interview is scheduled for 19th April 2026 in Bangalore, with job location at Bachupally, Hyderabad. Multiple openings across QA and QC departments make this a strong opportunity for candidates aiming to work in biologics and biosimilar manufacturing environments.

Company Overview

Dr. Reddy’s Biologics is a leading division of Dr. Reddy’s Laboratories, focused on developing and manufacturing high-quality biosimilars and biologics for global markets. The organization operates with strict adherence to international regulatory standards such as cGMP, USFDA, EMA, and data integrity frameworks.

With advanced R&D capabilities and cutting-edge biologics manufacturing facilities, Dr. Reddy’s Biologics plays a critical role in improving access to affordable biologic therapies worldwide. Professionals joining the company gain exposure to complex biologics processes, regulatory audits, and high-impact healthcare innovation.

Job Role & Responsibilities

Quality Assurance (QA) Associates

• Oversee analytical QA activities including batch record review and QC compliance
• Ensure adherence to QMS, cGMP, and ALCOA data integrity principles
• Handle investigations such as OOS, OOT, and CAPA implementation
• Support audit readiness and regulatory inspections

Drug Product QA

• Monitor formulation, filling, inspection, and packaging operations
• Ensure GMP compliance on shop floor and documentation accuracy

Development QA

• Review SOPs, manage document control, and support risk assessments
• Handle specification reviews and QbD-based process improvements

Drug Substance QA

• Support upstream and downstream manufacturing QA activities
• Ensure in-process compliance and documentation integrity

IT Quality Assurance

• Manage CSV validation, IT compliance, and data integrity systems
• Support audit readiness and regulatory expectations

AUM & SIT QA

• Conduct environmental monitoring and microbiological compliance activities
• Perform root cause analysis and CAPA for quality investigations

Quality Control (QC) Associates

Microbiology

• Perform sterility testing, BET, and microbial limit testing (MLT)
• Ensure GLP/GMP compliance and documentation accuracy

Analytical & In-Process QC

• Perform chromatography techniques such as HPLC, SEC, IEX, and Glycan analysis
• Execute in-process testing aligned with manufacturing timelines

Molecular Biology & Bioassay

• Conduct assays like PCR, ELISA, SDS-PAGE, CE-SDS, western blot, and FACS
• Perform cell-based bioassays and analytical testing for biologics

QC Compliance & LIMS

• Manage documentation, deviation handling, CAPA, and compliance monitoring
• Support LIMS operations and audit readiness

Lab Support

• Manage sample handling, calibration coordination, and inventory control
• Ensure uninterrupted QC laboratory operations

These roles are essential in ensuring product quality, regulatory compliance, and safe biologics manufacturing processes that directly impact patient outcomes.

Eligibility / Qualifications

Required Education:

Bachelor’s or Master’s degree in Life Sciences

Relevant Courses:

Biotechnology, Microbiology, Biochemistry, Molecular Biology, Pharmaceutical Sciences, Life Sciences, Bioinformatics

Experience:

• 3 to 10 years of experience in QA or QC roles within pharma/biologics industry
• Strong knowledge of GMP, GLP, and regulatory compliance
• Hands-on experience in analytical techniques, microbiology, or biologics testing

Location & Salary

• Job Location: Bachupally, Hyderabad
• Interview Location: Aurigene Oncology Limited, Electronic City, Bangalore
• Salary: Competitive salary package based on experience and industry standards

Application Process

Candidates can attend the walk-in interview directly:

Date: 19 April 2026
Time: 9:00 AM onwards
Venue: Aurigene Oncology Limited, KIADB Industrial Area, Phase II, Electronic City, Bangalore

Candidates may also apply via the official application process using QR code shared in the job advertisement.

This is a premium opportunity for professionals seeking biotech jobs, pharma QA jobs, QC analyst roles, and biologics careers with a globally recognized organization.

Why Join Dr. Reddy’s Biologics?

• Work in a globally recognized biologics and biosimilars organization
• Exposure to advanced analytical techniques and regulatory systems
• Strong career growth in biologics, QA, and QC domains
• Opportunity to work on cutting-edge healthcare solutions

Frequently Asked Questions (FAQs)

Who can apply for these roles?

Candidates with Bachelor’s or Master’s degrees in life sciences and 3–10 years experience can apply.

What departments are hiring?

Quality Assurance and Quality Control across multiple specialized domains.

Is biologics experience required?

Preferred but candidates with strong pharma QA/QC experience may also be considered.

What skills are important for selection?

Knowledge of GMP, analytical techniques, regulatory compliance, and investigation handling is essential.

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Summary Table

Company	Dr. Reddy’s Biologics
Vacancies	QA Associate, QC Associate (Analytical, Microbiology, Bioassay, Molecular Biology, Compliance)
Required Education	Bachelors/Masters in Life Sciences
Experience	3–10 Years