Senior Research Associate - Product Analytics

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.

Roles & Responsibilities

• Routine analysis support, method development and qualification.
• Execution of critical experiments for specific deliverables.
• Error free analysis and documentation.
• Involve in report preparations, report closures and technology transfer of assays.
• Prepare protocol / report / manuscript as needed, including contributions to writing and reviewing content.
• Collaborate with cross-functional teams to support development projects.
• Stability charging and analysis on time.
• Monitoring of timely and effective execution of HPLC/UPLC calibration and maintenance of equipment/ instruments/columns.
• Participation in Quality and Safety related initiatives, activities and their timely closures.
  

Qualifications

Qualifications

Educational qualification and Experience:

Ph.D.

0 to 1 years of Industrial experience

Masters

Technical Skills

• Basic knowledge of protein structure, characterization, stability, therapeutic proteins like monoclonal antibodies.
• Basic understanding of relevant techniques like HPLC, Electrophoresis, Spectroscopy, Basic Chromatographic techniques (affinity, SEC, IEX, RP etc). Method development and qualification.
• Basic understanding of protein-protein interactions, encompassing principles of ELISA (Enzyme-Linked Immunosorbent Assay) and western blotting techniques.

Behavioural skills

• Learning orientation, seeking opportunities for personal and professional development.
• Stakeholder orientation, focusing on understanding and meeting the needs of various stakeholders involved.
• Ability to build relationships, fostering positive connections with colleagues, clients, and other stakeholders.
  

Additional Information

About the DepartmentBiologics