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Principal Engineer, System Verification

https://www.baxter.com/ Logo

Baxter

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Location:
India , Bengaluru

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

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 Responsibility:

  • Provides technical leadership for Medication Delivery System Verification
  • Lead technical team members in the application of standard system engineering principles, methods, and techniques to resolve difficult problems focused on system verification
  • Plans and leads project assignments in the evaluation, selection and adaptation of various techniques, procedures, and criteria with minimal guidance
  • Reviews and approves verification plans and methods and provides general direction to verification engineering staff
  • Ensures that quality is built into the design during new product development
  • Reports out on the progress to senior management
  • Contributes to System Verification Engineering vision that aligns with the organization's vision and strategic plan
  • Provides direction to technical team members that are accountable for system verification engineering activities
  • Provide Technical direction for Systems Verification and Validation Engineering staff and programs
  • Lead the planning, development and execution of system verification and validation deliverables (test plans, test protocols, test cases, test reports, studies)
  • Contribute to the development and documentation of system requirements, systems architecture and design
  • Ensure appropriate traceability between system, subsystem, verification/validation and cross functional deliverables
  • Manage the integration of deliverables from subsystem teams, cross functional teams (risk management, compliance, etc.) and external partners
  • Resolve competing constraints between interrelated functions (Engineering, Risk Management, Compliance, Reliability, Clinical, Human Factors, Regulatory)
  • Implementing configuration and change management through the complete product life-cycle, including verification and validation deliverables
  • Actively communicates and advocates team’s capabilities and accomplishments
  • Recommends changes to policies and establishes procedures that affect immediate department/function
  • Create opportunities to automate testing and optimize test processes
  • Create best practices and process improvements to streamline testing between system verification, subsystem and software verification
  • Ensures all program milestones in support of all phases of the product development lifecycle are completed on time, with appropriate quality, and in compliance with relevant laboratory standards and regulations
  • Participates and/ or leads design reviews
  • Guides the team in the state of art V&V practices, QMS processes and on the applicable regulations / Standards, country specific requirements
  • Maintains an effective and collaborative working relationship with internal and external development partners across all levels and diverse cultures
  • Guides the team in investigations for identifying the root cause and drives action to prevent such issues recurring
  • Collaborate with other engineering teams within the organization
  • Guide, mentor, and provide direction to junior verification and validation Engineers
  • Ensure compliance to the product development process and Quality System requirements
  • Ensures good documentation and Good Manufacturing practices are followed in the Verification and Validation Process

Requirements:

  • Bachelor’s Degree in mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent, with approximately 10+ years of relevant industry experience
  • Healthcare industry experience preferred
  • Requires strong organization and communication skills, with the ability to interface with both technical and non-technical personnel
  • Strong knowledge of ISO, FDA and other regulatory standards is essential
  • Hands on experience in data analysis of Performance testing and Sample size calculations for variable/Attribute data
  • Experience in Tools like Minitab(Data Analysis) /JIRA ( Defect )/ALM ( test Environment) etc.
  • Demonstrated experience working with vendors with different models of engagement
  • Knowledge of Design controls, lifecycle testing processes, MTBF analysis
  • Must have demonstrated effective supervisory and people development skills
  • Ability to lead teams across multiple sites
  • Ability to convince management on courses of action with minimal assistance using both written and verbal methods

Nice to have:

System Verification Engineers with Experience in Infusion pumps design verification testing

What we offer:
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer

Additional Information:

Job Posted:
April 24, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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