Team Member - Quality Control

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

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.

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 maintain analytical instruments like HPLC, GC, Dissolution apparatus, FTIR, KF, etc.
Perform routine checks, system suitability, and troubleshooting.
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.

M.Sc (Chemistry), B.Pharm

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.