Research Associate I

4 weeks ago

Bengaluru Karnataka, India BAXTER Full time

**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**
- **Job Title - Research Associate I**:

- **Location - Whitefield, Bangalore**:

- **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 cross-functions.
- 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 cross-functional 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 cross-functions 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 problem-solving skills
- Good organizational skills. Ability to effectively organize and prioritize tasks.

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, disability/handicap status or any other legally protected characteristic.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

**Reasonable Accommodations**

**Recruitment Fraud Notice**

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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