Quality Control Associate- Material analytics

SmartRecruiters, Inc.; Hyderabad; On-site; INR 500,000 - 750,000; Full time

Benefits offered by this job

Joining & relocation support

Medical coverage

Life coverage

Job summary

Dr. Reddy’s Laboratories Ltd. seeks a detail-oriented Raw Material Testing Specialist for its DS manufacturing facility. You will perform sampling, chemical testing, and batch release activities to ensure quality and regulatory compliance of raw materials used in production.

The role requires a Master’s degree in Chemistry or Life Sciences and 2–5 years in a lab setting, preferably in pharma. Expect collaboration with QA/Production, meticulous record-keeping, and strict GDP/GMP adherence.

Qualifications

• Master’s degree in Chemistry or Life Sciences or related field.
• 2–5 years’ experience in a laboratory setting, preferably pharma.
• Knowledge of GMP, GDP, and regulatory requirements.

Responsibilities

• Sampling of raw materials according to 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.

Skills

Sampling

Chemical testing

Batch release testing

GMP compliance

LIMS handling

GDP documentation

cGMP knowledge

Analytical troubleshooting

Education

Master’s degree in Chemistry or Life Sciences

Job description

Quality Control Associate- Material analytics

• Full-time
• Job Family: Quality
• Sub Job Family: Quality Control
• Business unit: Biologics

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).

‘TheNextand 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: Technical Skills

• 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.

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.

Biologics

Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.

With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.

With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.

Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.

We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure

Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.

Benefits Offered

At Dr. Reddy’s we actively help to catalise your career growth and professional development through personalised learning programs.

The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.

Our Work Culture

Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.

For more details, please visit our career website at https://careers.drreddys.com/#!/

We believe in the power of unity, where diverse skills, a common purpose, and shared values spark magic

Who we are We accelerate access to affordable and innovative medicines because...