Research Associate Iii

1 month ago

Bengaluru Karnataka, India BAXTER 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.

**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 - Principal Engineer/Research Associate III**:

- **Location - Whitefield, Bangalore**:

- **Shift - General**

**Job Responsibilities and Skills**:

- As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front
- Broad understanding of the overall product and therapy along with deep technical expertise in one or more fields related to drugs and medical devices
- Prior experience of handling large and complex projects related to drugs and medical devices
- Technical leadership in Lifecycle management and new product development in drugs/medical devices
- Prior experience with the new product and process development in the area of drugs, medical devices and combination drug/device systems
- Understanding of structure property relationship of new materials in the domain of drugs/medical devices
- Prior experience of managing diverse and cross functional teams at a global front
- Sound understanding of invention disclosures and patent filing processes
- Lead multi-functional project team for effective collaboration and deliverables
- Understanding of regulatory, process development, quality management systems, QbD tools, drug modelling and design of experiments in the field of drugs and medical devices
- Understanding of Compounding, extrusion and injection molding processes for new materials development
- Good knowledge of product development stages, Bio design process and life cycle management in the area of drugs and medical devices
- Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs
- Propose options and develop action plans for problem-solving, product and process inventions and improvements
- Establish, maintain and update technical & Design documentation as needed according to Good Documentation Practices
- Active participation in the audits as the role demands and prior such experience would be desired
- Fluent with Technical Writing, Documentation and reports generation
- Influential leadership and ability to flex as the role demands while interacting with internal and external stakeholders
- Out of the box and critical thinking ability
- Being able to anticipate risks/challenges and willingness to deal with ambiguity

**Qualifications**:

- Ph.D/Masters in Pharmaceutics, Material Science, Polymer Chemistry, Polymer Engineering, Chemical Engineering, Biology, Biosciences and Biomedical engineering
- Minimum of 8 years of diverse industrial experience post Ph.D and about 10 years post Masters in the given technical domains of interest
- Desired if the incumbent had more than one jobs/roles and has interacted with many different global stakeholders in a given role
- Clear and effective communication (written, oral) and presentation skills.
- Good stakeholder management (local and global)
- A proven track record of effectiveness in a fast-paced environment.
- Proven ability to create results within budget, timeline, and product/project deliverables

**Skills**
- Adequate orientation towards Renal therapies and products with time
- Good knowledge of Design Control documentation and medical writing
- Sound knowledge of international/regional/national regulations and standards for drugs and medical devices
- Acquire business acumen with time
- Demonstrate strong project management and people leadership skills
- Ability to work independently
- Experience with Statistics and Six Sigma tools
- Can effe

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