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.

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A Quality Control Analyst is responsible for performing analytical testing of raw materials, in-process samples, finished products, and stability samples in compliance with GMP, regulatory guidelines, and company SOPs. The role ensures accurate, reliable, and timely reporting of results to support product quality and batch release.

Key Responsibilities:

1. Analytical Testing

• Perform analysis of RM, PM, in-process, finished products, and stability samples.
• Operate analytical instruments such as:
  • HPLC, GC, UV, IR, KF, Dissolution Apparatus
• Ensure proper documentation of analytical data.

2. Data Handling & Documentation

• Record results in LIMS / worksheets / logbooks as per GDP practices.
• Review data for accuracy and completeness before submission.
• Maintain raw data traceability and integrity.

3. Instrument Handling

• Perform routine calibration and system suitability checks.
• Ensure proper maintenance and cleaning of instruments.
• Report any instrument malfunction to the supervisor.

4. Compliance & GMP

• Follow cGMP, GLP, and data integrity requirements (ALCOA principles).
• Adhere to SOPs, STPs, and safety guidelines.
• Participate in audits and provide required data/documents.

B.Sc / M.Sc (Chemistry / Analytical Chemistry) or B.Pharm 

Required Skills:

• Knowledge of analytical techniques and instrumentation
• Understanding of GMP, GLP, and regulatory requirements
• Familiarity with Empower / LIMS systems
• Good documentation and data integrity practices
• Attention to detail and accuracy
• Basic investigation and problem-solving skills

Key Competencies:

• Strong analytical mindset
• Accountability and ownership
• Time management (meeting batch timelines)
• Team coordination
• Compliance-focused approach