Associate Scientist II, R&D-ADL

This is where your work makes a difference.

At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job-you will find purpose and pride.

Essential Responsibilities :

• . Responsible for Analytical Method Transfer activity at Baxter and Non-Baxter Manufacturing sites.
• . Oversee and lead all activities of assigned team / projects to meet customer needs.
• . Work according to appropriate standards for quality, ethics, health, safety, environment, protection and information safety as per company policy.
• . Communicate, address and solve problems within own and broader area of responsibility. Communicate effectively across organizational interfaces.
• . Oversee and write transfer protocols, transfer reports, lab procedures or process related SOPs. Write scientific documents intended for external partners or for generation of registration documents.
• . Proactively communicate key issues and any other critical topics in a timely manner to the manager and / or to any other relevant project team members.
• . Prepare and revise the specification and Method of analysis for API, FP, Excipient and Packaging materials in close co-ordination with CFTs / Manufacturing site.
• . Responsibility for review of DMF for specifications and analytical method including method validation for all the tests in API and Excipients and review from suppliers and implementation of declarations (Residual solvents, Elemental impurity, Nitrosamine Impurity etc.) at Baxter.
• . Responsible for Prepare and Update documents as per the Supplier Notifications Change (SNC) related documents for API, Excipient and Packaging related material and their implementation at Manufacturing site.
• . Preparation of documents against Compendial changes, based on their assessment from CFTs (F&D, RA, PQ, Product Design team, Plant / CMOs and PMT) and its timely implementation at respective manufacturing Sites.
• . Serve as subject matter expertise in the areas of analytical chemistry internally and externally as needed.
• . Responsible for Quality change control procedure, CAPA, NCR, etc in TW8 and maintaining quality matrix.
• . Collaborate with Baxter external partners to ensure successful execution of analytical testing and study designs.

Skills Required :

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability / handicap status or any other legally protected characteristic.

Reasonable Accommodations

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Skills Required

method transfer , analytical method validation , Analytical Techniques, Team Management, Effective Communication