Research Associate I

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.
• Innovative ideas generation for new 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 Good Documentation Practices

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