High-Growth Pharma QC Job at Dr Reddy’s Laboratories | B Pharm Graduates | Apply Now
Looking for a Pharma QC Job with a leading pharmaceutical company? Dr Reddy’s Careers offers an exciting opportunity for B.Pharm professionals to join as Team Member – Quality Control in Hyderabad. This Pharma QC Job provides hands-on experience with advanced analytical instruments while building a rewarding career through Dr Reddy’s Careers in a globally recognised pharmaceutical organisation.
- Position: Team Member – Quality Control
- Location: Hyderabad
About the Company
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company committed to accelerating access to affordable and innovative medicines worldwide. Founded in 1984, the company has grown into a global healthcare organization with research and development centres, manufacturing facilities, and a commercial presence in 66 countries. Through its purpose-driven approach, strong scientific foundation, and commitment to sustainability, Dr. Reddy’s continues to improve the lives of millions of patients across the globe.
Job Description
Quality Control Analyst will be responsible for performing analysis of raw materials, in-process samples, finished products, and stability samples in compliance with approved specifications, SOPs, and regulatory requirements (cGMP, USFDA, ICH). The role involves handling analytical instruments, ensuring data integrity, and maintaining documentation as per audit standards.
Key Responsibilities
- Perform analysis of API, excipients, in-process, finished products, and stability samples.
- Execute testing using instruments such as HPLC, GC, UV-Visible Spectrophotometer, Dissolution, KF, IR, etc.
- Ensure adherence to approved STPs, specifications, and SOPs.
- Operate and maintain analytical instruments like HPLC, GC, Dissolution apparatus, FTIR, KF, etc.
- Perform routine checks, system suitability, and troubleshooting.
Qualifications
- B.Pharm
Required Skills
- Strong knowledge of analytical techniques (HPLC, GC, etc.)
- Good understanding of cGMP, data integrity, and regulatory expectations
- Familiarity with LIMS and electronic data management systems
- Good documentation and communication skills
- Must have experience in Empower and LIMS software.
Additional Information
- Record all raw data in notebooks / LIMS systems as per ALCOA+ principles.
- Ensure proper documentation with no overwriting, no loose sheets, and traceability.
- Review analytical data for accuracy and compliance.
- Follow cGMP, GLP, Data Integrity (DI), and regulatory guidelines.
- Assist in OOS, OOT, deviation, and incident investigations.
- Support root cause analysis and implementation of CAPA.
- Perform stability sample analysis and trending.
- Ensure timely completion of assigned samples.
