QC associate

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, color 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 an associate for the Quality control -Analytical team responsible for conducting  analysis of  Biosimilar products ( drug substance , drug products and their in-process samples and stability samples). The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety.

" Roles & Responsibilities

• To perform analysis in Quality control analytical laboratory for the Biosimilar /Biologics Products as per the planning allotted by Team lead
• To perform chromatography techniques like RP-HPLC, Glycan, SEC, IEX, pep map for Biosimilar Molecules
• Having 2 to 6 years of experience
• Method Validations on RP-HPLC, Glycan, SEC, IEX, pep map
• To Perform Biochemical, Physico chemical and chromatographic analysis
• Adhering to GMP practices
• Adhering to Good documentation practices
• Adhering to Good Analytical Practices
• Adhering to Regulatory Requirements including Internal or External audits, Audit readiness and Query response drafting.
• Adhering to compliance of systems in Quality Control, by working with relevant stake holders
• To adhere and follow the safety practices and procedures.
• To adhere to various cGMP procedures and internal SOPs

Educational qualification:

A Masters' degree in Biotechnology/ BE Biotechnology/B Tech Biotechnology or in Biochemistry domain.

Minimum work experience:

2 to 6 years of experience in QC analytical testing in Biosimilar products

Skills & attributes: Technical Skills

• Proficient in handling SEC/RP/IEX/Peptide Mapping/Glycan analysis of Biosimilar Products
• Proficient in handling of Gel electrophoresis/CE/HCP/HCD analysis of Biosimilar products
• Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications.
• 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.
• Method Validations on HCP/HCD/CZE/SDS PAGE

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.

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...

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