Research Associate I, R&D - F&D - #978106

Baxter Medical Devices


Date: 3 days ago
City: Ahmedabad, Gujarat
Contract type: Full time

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives-where your purpose accelerates our mission.

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.
. 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

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information.

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