Research Associate Ii - Bengaluru, Karnataka, India - BAXTER

BAXTER

Verified Company

Bengaluru, Karnataka, India

1 week ago

Posted by:

Deepika Kaur

beBee Recuiter

Description

Vantive:
A New Company Built On Our Legacy
Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company.

Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre.

Each of us are driven to help improve patients' lives worldwide. Join us as we revolutionize kidney care and other vital organ support.
About Baxter

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services.

The company's global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.

Baxter's employees worldwide are building upon the company's rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

Job Summary
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Job Title

Research Associate I:

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Location

Whitefield, Bangalore:

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Shift

General

Research Associate I within Renal Business, is responsible for technically leading projects/tasks/activities related to product development and lifecycle management of Peritoneal Dialysis products.

Duties and Responsibilities

As Tech Lead or Change Owner, define, organize, plan, and execute activities related to product design change, supplier related changes, new product registration and strategic or value improvement projects in compliance with current international/regional/national regulations with support from senior colleagues as in when necessary.
Propose, formulate, and coordinate action plan for implementation of changes and related activities by working closely with PDO Organization, Project Management, Regulatory, Quality, senior colleagues, and the other crossfunctions.
Expected to develop, document, test and manage product related changes in accordance with established Renal Care product processes and stay in alignment with Quality Management System.
Ensure good internal and crossfunctional communication and regular status update of activities.
Establish, maintain, and update Technical & Design documentation according to Good Documentation Practices.
Propose, participate, or lead ideation sessions for product enhancement and exploratory activities to foster innovation culture within team.
Ensure Quality & Compliance to Baxter policy/Ethics/Data Integrity.

Qualifications

Masters in Science or Pharmaceutical disciplines is required. Must be able to interact on a technical level.

Education and Experience

Master's degree in Science or Pharmaceutical disciplines is required with relevant experience.
Adequate orientation towards Renal PD therapies and products with time.
Adequate knowledge of product development stages and life cycle management required for effective collaboration with crossfunctions and execution of project deliverables.
Adequate knowledge of Design Control documentation, Process, and Quality Management Systems.
Adequate knowledge of international/regional/national regulations and standards.
Demonstrate Project Management skills in due time.
Demonstrates flexibility and the ability to shift gears between projects comfortably.
Excellent oral and written communication skills.
Good analytical and problemsolving skills
Good organizational skills. Ability to effectively organize and prioritize tasks.

Reasonable Accommodations

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