Bangalore, Karnataka
3 days ago
Principal Eng, Quality Assurance

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. 

Job Description: -

This Principal Engineer, Quality Assurance position falls within a growing team for Software Quality. This person will work as a member of one or more cross-functional product development teams by being engaged in new product development and/ or sustaining products covering emerging technologies such as Digital Health, Health Software, Software as a Medical Device (SaMD) and Clinical Decision Support (CDS). This individual will serve as a quality representative on the software project team and will work closely with the Core Team Leader. This role is responsible for ensuring that each project is developed and released meeting customer expectations and in compliance with Baxter’s software lifecycle management policies and procedures. This Principal Engineer will work closely with product engineering to ensure robust requirements, successful design, development, verification and validation testing, design transfer and change control management. In addition, this individual will provide support to product software sustaining engineering and support the creation of regulatory submission documentation.

Qualifications: -
• Bachelor’s degree in engineering or computer science with a minimum 10 years of experience in a highly regulated industry such as FDA, DoD, aerospace or telecom with a thorough understanding of the regulations, standards, Software Development Life Cycle (SDLC) and quality management systems.
• Experience in assessing and developing procedure to meet Digital Health regulatory requirements and guidance’s.
• Experience with FDA inspections. ISO/ Notified Body audits is a plus.
• Experience in the application of design controls and compliance requirements in accordance with 21 CFR Part 820, 803, & 806, IEC 62304, ISO 13485, ISO 14971, EU MDR, 21st Century Cures Act, NIST Cybersecurity framework, FDA pre and post market cybersecurity guidance, AGILE SDLC for the development of SaMD/CDS and Health Software products.
• Professional certification such as ASQ, IEEE, Six Sigma, LEAN manufacturing or achievement of certification. ASQ CSQE preferred.
• Strong communication and leadership skills.
• Strong, results driven, project management skills.
• Excellent problem-solving skills and the ability to teach others.
• Capable of clearly presenting and justifying quality position and requirements to management.
• Hands-on Experience on Software development is added Advantage.

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

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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