Job Summary

This position involves active contribution to the Formulation ARD team in technical and operational activities such as hands-on support to formulation development in parenteral formulations and interpretation of analytical results. The incumbent will perform other duties as assigned.

Responsibilities
Literature search for the respective product/project and make a consolidated report.
Define, organize, plan and execute QbD-based experiments to develop pharmaceutical injectables in compliance with current international/regional/national regulations with the support of senior colleagues and team members.
Analysis of the experimental study outcome and present the data to the team for the further action plan.
Independently analyze and propose solutions to research problems based on understanding.
Engage in root cause analysis in new product development and sustaining product projects under supervision.
Understanding of the manufacturing process to assess the impact on the product quality under supervision.
Apply technical theories and principles to projects within area of expertise.
Scale up and plant support for technology transfer of injectable products.




Cutting-edge ideas generation for recent project development.
Document laboratory work performed per Baxter s GDP.
Work according to appropriate standards (e.g., Data Integrity, ALCOA) guidelines.
Follow Baxter s Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S;) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement.
Provide support as needed in calibration and maintenance of equipment in the laboratory.
Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders, with respect to project commitment, quality procedures, and business needs
Establish, maintain, and update technical & Design documentation according to Valuable Documentation Practices

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📌 Research Associate I Ahmedabad (India)
🏢 BAXTER
📍 India