- Full Time
- Hyderabad

Website Dr. Reddy’s Laboratories Ltd.
📍 Location: Hyderabad, India
📅 Application Deadline: 30th March 2025
Table of Contents
ToggleAbout Dr. Reddy’s Laboratories Ltd.
Dr. Reddy’s Laboratories Ltd. is a global leader in the pharmaceutical industry, dedicated to delivering high-quality, affordable, and innovative medicines. With over 24,000 employees worldwide, we are committed to our mission: “Good Health Can’t Wait.”
Role Overview
We are looking for a DQA Associate to ensure compliance in manufacturing and quality processes. This role involves reviewing real-time investigations, monitoring batch manufacturing and testing activities, and maintaining adherence to regulatory and global quality standards.
Key Responsibilities
- Oversee in-process activities during shifts, including line clearances, material verification, machine start-up, and sample collection.
- Ensure accurate documentation of batch records, log books, and quality assurance (QA) activities.
- Maintain compliance with the Quality Management System (QMS), including incident management, change control, and CAPA implementation.
- Monitor adherence to Good Manufacturing Practices (GMP) by ensuring facility upkeep, proper segregation of materials, and environmental conditions.
- Support investigations related to batch failures, complaints, Out-of-Specification (OOS) results, and deviations.
- Coordinate cross-functional teams for root cause analysis, CAPA implementation, and effectiveness monitoring.
- Assist in internal and external audits, provide required documentation, and track action item closures.
Candidate Profile
🎓 Qualification: B.Pharm or Post-Graduation (Life Sciences)
📅 Experience: Minimum 4 years in Manufacturing, Quality Assurance, Quality Control, or Engineering & Development.
Required Skills & Attributes
✅ Strong understanding of Quality Systems and regulatory requirements (FDA, EU, Indian Authorities).
✅ Knowledge of Bio Pharma and Pharma markets, including industry trends and product insights.
✅ Familiarity with cGMP regulations and compliance procedures.
✅ Proficiency in documentation, reporting, and audit handling.
✅ Excellent communication, analytical thinking, and problem-solving skills.
✅ Ability to work collaboratively in a team-oriented environment.
Industry & Functional Area
🏢 Industry: Pharma / Healthcare / Clinical Research
🔬 Functional Area: Biologics
If you are passionate about quality assurance and want to contribute to delivering high-quality medicines, we invite you to apply!
📩 Apply now and be part of our mission: “Good Health Can’t Wait.
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