Analytical Scientist Topical

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

Roles & Responsibilities

• Conduct Literature survey and prepare analytical strategy for assigned projects & Should have minimum understanding of DMF and test methods of drug substance, etc.
• Perform analytical method development of Viscosity, PSD, GSD, Assay, RS, preservative content, residual solvents, rheology, IVRT etc
• Conducting of method validation and method development. Preparation of new specifications/STP’s and COAs. Integration inputs from QA, QC and RA members.
• Execution of method feasibility studies for compendia procedures of excipients/API/FP
• You will be responsible for analytical methods and process compliance as per quality assurance requirement.
• Perform calibration or performance verification of analytical equipment; Maintain & standardize reference or working standards; Check for the availability and validity of the Impurities.
• Perform the assigned day to day routine analysis of development, stability samples, scale-up, PE batches.
• Execute assigned analytical activities as per defined procedures, document the data and send the respective record of analysis of to group leader for the review and release IN ORDER TO provide the approved results to formulation team.
• Co-ordinate with other departments (CFTs) for procurement, analytical method transfer activities, specification finalization etc.
• Perform method transfers to plant QC, customers or Third party labs for projects and support at the time of exhibit/submission batch execution.
• Adhere to the safety guidelines, applicable ISMS guidelines, SOPs, equipment usage and maintenance procedures.
• Conducting studies at external CRO labs to manage peak workloads or when internal capabilities are not available. Providing technical support to CRO labs for smooth execution of studies.
  

Qualifications

Education Qualification -

Additional Information

About the DepartmentGlobal Generics India