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.
•Tracking of online submissions, query responses & approvals for medical devices applications & Import and registration division applications on SUGAM portal
•Establish robust relationship with country regulatory authorities to facilitate technical and strategic discussions related to product.
•Monitoring of country regulatory changes and assessment per se their impact on current product portfolio.
•Build strategies for country regulatory changes and communicate to Global and country cross functional teams.
•Ensure product life cycle management for all registered products in India & adjoining countries. To ensure timely closure of all labelling changes (with global) per se India specific labelling requirements and creation of local labels with India specific requirements for devices prior to custom clearance and commercialization
•Responsible for change control assessment from regulatory perspective and timely reporting of post approval changes to respective regulatory authorities.
•Timely filing of product recalls/complaints notification as per SOP to regulatory agency.
•Responsible for timely release of port consignments (Air and Sea) for commercialization of product to meet business demands.
•Responsible