Pharma QA Job at Dr. Reddy’s Laboratories
Looking for Pharma QA Jobs with a leading pharmaceutical company? Dr. Reddy Careers is hiring a Quality Assurance Specialist – Analytical Compliance for professionals with a background in Pharmacy, Chemistry, or Analytical Chemistry. The role focuses on QC laboratory compliance, analytical data integrity, OOS/OOT investigations, CAPA, change control, method validation, and regulatory compliance.
- Position: Quality Assurance Specialist – Analytical Compliance
- Function: Quality Assurance / Analytical Compliance
About the company
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company operating in the global healthcare space. With over 24,000 employees, the organization is dedicated to accelerating access to affordable and innovative medicines. The company has a presence in 66 countries and is committed to sustainability, aiming to reach over 1.5 billion patients worldwide by 2030. As a strong advocate for diversity and inclusion, Dr. Reddy’s fosters a work environment free from discrimination, ensuring equal opportunities for all.
Job Description
The Quality Assurance Specialist will play a crucial role in maintaining compliance within the QC laboratory. Responsibilities include participating in investigations of Quality Management System (QMS) documents, preparing trending reports, evaluating Change Controls and CAPA action plans, and reviewing all analytical data generated in the laboratory. This position is essential for ensuring that Dr. Reddy’s Laboratories upholds its commitment to quality and regulatory compliance in all its operations.
Key Responsibilities
- Participate in investigations of QMS documents such as OOS, OOT, and laboratory deviations, ensuring timely closures.
- Prepare trending reports for OOS, OOT, and laboratory incidents to support CAPA identification and process improvements.
- Evaluate Change Controls and CAPA action plans, verifying their effectiveness to resolve root causes.
- Review all analytical data generated in the Quality Control laboratory for accuracy and compliance.
- Review instrument and equipment calibration records to confirm reliability and GMP adherence.
- Prepare and review documentation related to stability samples and ensure proper maintenance of related records.
- Perform and verify SAP transactions related to laboratory workflows and data entries.
- Review and approve method validation and transfer protocols and reports to ensure analytical consistency.
Eligibility Criteria
- Educational Qualification: Graduation in Chemistry/Analytical Chemistry or Pharmacy is mandatory; a Master’s degree is preferred.
- Minimum Work Experience: 2+ years in a relevant field.
Required Skills
- Regulatory Compliance
- Technical Documentation
- Change Control
- Laboratory Information Management
- Risk Management
- Chromatography
- Good Manufacturing Practices (cGMP)
- Quality Management Systems (QMS)
Why Join Dr. Reddy’s Laboratories?
Dr. Reddy’s Laboratories is dedicated to fostering a culture of empathy and dynamism, where employees are encouraged to grow and develop professionally. The organization’s commitment to sustainability and innovation makes it a leader in the pharmaceutical industry. Employees enjoy a supportive work environment, comprehensive benefits, and opportunities for personal and professional growth. The company’s motto, “Good Health Can’t Wait,” reflects its mission to empower people and improve lives globally.
In summary, the pharma QA job at Dr. Reddy’s careers offers an exceptional opportunity for qualified candidates to contribute to quality assurance in the pharmaceutical sector. With a focus on compliance and analytical integrity, this role is pivotal in supporting the company’s mission. Interested candidates are encouraged to apply before the deadline to be part of this esteemed organization.
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