Dr. Reddy’s Careers Hiring for Quality Assurance Jobs | Apply Now
Searching for rewarding Quality Assurance Jobs in the pharmaceutical industry? Dr. Reddy’s Careers is hiring for the Team Member – Analytical Quality Assurance role in Andhra Pradesh. This Chemistry Jobs opportunity is ideal for professionals with experience in QA/QC laboratory operations, analytical compliance, GMP, GLP, documentation review, and regulatory standards. Candidates passionate about pharmaceutical quality systems and analytical excellence should not miss this opportunity.
- Job Title: Team Member – Analytical Quality Assurance
- Location: Andhra Pradesh
About the Company:
Dr. Reddy’s Laboratories is a globally recognized multinational pharmaceutical company dedicated to accelerating access to affordable and innovative medicines. Established in 1984, the company operates across 66 countries with a strong focus on research, sustainability, quality, and scientific innovation. Through Dr. Reddy’s Careers, professionals gain opportunities to work in a future-ready environment driven by integrity, compliance, and continuous learning.
Job Overview:
The Team Member – Analytical Quality Assurance role focuses on ensuring compliance within Quality Control laboratory operations and analytical systems. Professionals will participate in investigations related to OOS, OOT, deviations, CAPA, and change controls while ensuring adherence to GMP, GLP, and regulatory guidelines. The role includes reviewing analytical data, calibration
records, audit trails, stability study documentation, and LIMS protocols. Candidates will also manage SAP transactions, monitor QMS notifications, and support data integrity practices within pharmaceutical laboratory operations.Roles & Responsibilities:
- You will be responsible for participating in investigations of Quality Management System (QMS) documents such as OOS, OOT, and laboratory deviations, and ensuring timely closures as per SOP timelines.
- You will be responsible for preparing trending reports for OOS, OOT, and laboratory incidents, using analytical insights to support CAPA identification and process improvements.
- You will be responsible for evaluating Change Controls and CAPA action plans, verifying their effectiveness to ensure resolution of root causes and prevention of recurrence.
- You will be responsible for reviewing all analytical data generated in the Quality Control laboratory—including electronic and raw data—ensuring accuracy and compliance with relevant SOPs.
- You will be responsible for reviewing instrument and equipment calibration records and audit trails to confirm reliability, data integrity, and GMP adherence.
- You will be responsible for preparing and reviewing documentation related to stability samples and ensuring that reference standards, impurity standards, working standards, and related records are maintained per applicable procedures.
- You will be responsible for performing and verifying SAP transactions related to laboratory workflows and data entries as outlined in SOPs, ensuring traceability and accuracy.
- Management of QMS notifications through DCMS.
- Monitor and ensure cGLP (current Good Laboratory Practices) in Quality control and Micro Lab, and implementation of standard operating procedures.
- Verification of audit trails for all the GxP computer systems at Quality Control Laboratory.
- Preparation, Review, and approval of stability study protocols on LIMS.
- You will be responsible for reviewing and approving method validation and method transfer protocols and reports, as well as LIMS master data and control limit updates, ensuring analytical consistency across platforms.
Educational qualification:
- Graduation in Chemistry/Analytical Chemistry
- A Master’s in Chemistry/Analytical Chemistry is preferred
Minimum work experience:
- 2-4 years of experience
Skills Required:
- Knowledge of GMP, GLP, and QMS systems
- Experience with analytical compliance and documentation
- Understanding of regulatory standards and data integrity
- Familiarity with HPLC, GC, FTIR, and UV-Vis techniques
- Strong analytical and troubleshooting skills
- Knowledge of CAPA, OOS, OOT, and change controls
- Excellent communication and teamwork abilities
- Ability to manage technical documentation accurately
This Quality Assurance Jobs opportunity at Dr. Reddy’s Careers offers chemistry professionals an excellent platform to grow in pharmaceutical quality systems and analytical compliance. With exposure to advanced laboratory operations, GMP standards, regulatory practices, and analytical technologies, this Chemistry Jobs role can help candidates build a strong and rewarding career in the global pharmaceutical industry.
