Quality Control Associate- Material analytics

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.

We are seeking a detail-oriented and motivated Raw Material Testing Specialist to join our Drug Substance (DS) manufacturing facility. This role is critical to ensuring the quality, safety, and compliance of raw materials used in production. The candidate will be responsible for sampling, chemical testing, and batch release activities in accordance with GMP standards

Educational qualification: A Master’s degree in Chemistry/ Life Sciences, or a related field

Minimum work experience : 2 to 5 years of experience in the area laboratory setting, preferably in the pharmaceutical or related industry

Skills & attributes

Behavioural Skills

- Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks.
- Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates.
- Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities.
- Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations.
- Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities.

Requirements

Sampling of raw materials according to established SOPs and regulatory guidelines.; Conducting chemical testing using validated analytical methods (e.g., titration, spectroscopy, chromatography).; Performing batch release testing and documenting results to support manufacturing timelines.; Maintaining accurate records in compliance with GMP and regulatory requirements.; Collaborating with QA/Production teams to ensure timely approval and release of materials.; Troubleshooting analytical issues and supporting continuous improvement initiatives.; Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications.; Handle LIMS for sample login, data entry, and reporting.; Ensure all activities are documented contemporaneously in line with Good Documentation Practices (GDP); Maintain test records, equipment logs, and environmental data trends.; Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment).; Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents.