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Job Type

Full Time

Job Description

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.

Job Summary

  • You will be responsible to employ advanced analytical techniques such as Gas Chromatography with Mass Detector( GCMS/MS), Inductively coupled Plasma Mass Spectrometry (ICPMS) , Inductively coupled Optical emission spectroscopy (ICP-OES), Atomic Absorption Spectroscopy (AAS), Ion Chromatography (IC) and other specialized techniques to analyse and characterize materials.
  • You will be responsible to design and execution of experiments and the analysis of data. Also find the critical parameters and develop innovative solutions to complex problems in pharmaceutical research and development
  • You will be responsible to deduce the chemical structure and composition of complex molecules, compounds, and materials, elucidating their atomic and molecular arrangements using advanced analytical methods.
  • You will be responsible to develop and optimize analytical methods and protocols to facilitate the accurate and efficient characterization of diverse materials, ensuring the reliability and reproducibility of results.
  • You will be responsible to perform comprehensive data analysis and interpretation of experimental results, employing statistical tools and software to extract meaningful insights into the structure, composition, and properties of the materials under investigation.
  • You will be responsible to actively contribute to research projects aimed at developing novel methods for the characterization and elucidation of complex structures and stay updated with the latest advancements in analytical techniques and technologies
  • You will be responsible to Collaborate with cross-functional teams, including chemists, material scientists, and engineers, to provide analytical support and contribute insights to research and development projects. Effectively communicate findings and recommendations to the team and stakeholders.
  • You will be responsible to ensure adherence to quality control standards and regulatory requirements in all analytical processes, maintaining high standards of accuracy, precision, and reliability in data generation and analysis.
  • You will be responsible to troubleshoot instrument-related issues and perform routine maintenance and calibration of analytical equipment to guarantee the accuracy and performance of instruments used in structural elucidation.
  • You will be responsible to maintain comprehensive records of all experimental procedures, results, and observations. Prepare detailed reports and presentations summarizing analytical findings, methodologies, and conclusions for internal and external stakeholders.
  • You will be responsible to adhere to strict safety protocols and guidelines while handling hazardous materials and operating complex analytical instruments. Ensure compliance with all relevant safety regulations and best laboratory practices.

Qualifications

Educational qualification:

  • Hands on experience on Elemental analysis techniques such as Inductively coupled Plasma Mass Spectrometry (ICPMS) , Inductively coupled Optical emission spectroscopy (ICP-OES), Atomic Absorption Spectroscopy (AAS).
  • Through understanding on ICHQ3D studies, Delamination studies, Extractable & Leachable studies and its analytical methods.
  • Understanding and experience on Gas chromatography with Mass Detector(GC-MS/MS) for method development and method validations for Nitrosamines analysis.
  • Expertise in method development and validation of Ion Chromatography (IC) methods in critical projects.
  • Experience in Instrument Calibration & trouble shooting.
  • Familiar with Current Good Laboratory Practices (CGLP).

Behavioural Skills

  • Excellent communication and interpersonal skills.
  • Ability to work with cross functional teams.
  • Strong analytical and problem-solving abilities.

Additional Information

About the Department

Integrated Product Development Organisation

Benefits Offered

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