Location
India | India
Job description
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.
Your Role at Baxter:
The role of Senior Engineer, S oftware V&V is to make technical contributions in understanding software / system requirements and developing/updating the test protocols & procedures for the new and / or existing products at Software Sub system and Software level. It includes verification and validation, performance, reliability and safety/regulatory related tests and executing the same, documenting the reports.
This position is based out of Bangalore and reporting to Software manager GSS/PSS .
Essential Duties and Responsibilities :
Review, Author, Execute, perform, summarize, report out software verification & validation test activities of software components to a full system device: Which includes but not limited to:
Test Plans, Test Procedures, User and Functional Requirements testing,
Design Verification,
Installation/Operational/Performance Qualification Protocols,
Traceability Matrices and
Final Reports.
Support compliance/ closure of Regulatory and Quality requirements before completing Design Outputs/ Program Deliverables.
Clear understanding of the elements of Risk Management, FMEA, Software reliability, and related V&V tasks .
Participate in the development of software Verification & Validation methodologies in accordance with applicable Quality/Regulatory requirements and industry best practices.
Diagnose, isolate and investigate problem reports. Drive product improvements and/or bug fixes.
Participate in identifying software Verification and validation scope by performing impact analysis by reviewing code changes for each release.
Ensure good documentation practices are followed in the software Verification and Validation Process
Participate in continuous improvement activities by supporting the implementation of process and product quality improvement initiatives.
Deep knowledge in test automation tools and realizing test automation suite.
Work closely with the auditees to understand the details and support with all relevant objective evidence .
Adheres to Baxter Quality Management system & supports quality audits.
Support on-going regulatory agency inspection readiness through the self-assessment program to include mock inspections and compliance with revised and emerging regulations.
Pair up with design & development team to start the testing early in the design cycle to ensure the requirements testability, design traceability & test coverage. Identify issues early to fix them . Refine the test plans and procedures through pre-verifications / Dry runs.
Interacts with design team to resolve tests-related technical issues.
Presents the findings / objective evidence and able to present with rationale with applicability / exclusions.
Identify and report any quality or compliance concerns and take immediate corrective / Preventive action as needed.
Your Team:
You will be r eporting to Software M anager GSS/PSS . This position does not have any direct reports. You will need to work collaboratively with R&D and cross functions .
Your Location:
The role is located in the BRD facility in Bangalore India .
What You’ll Bring:
Bachelor's Degree in Mechanical engineering , Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
7 to 10 yrs of experience in software Verification and validation testing of Software .
Relevant technical testing/reliability experience software testing .
An understanding of test methods and processes for Software verification and validation.
Experience in - writing system , subsystem-level and module level software verification and validation plans, procedures, Test Execution and Test report generation .
Understanding of software product design methodologies and test practices.
Familiarity with reliability theory and analysis as it pertains to test quantities derived from reliability.
Ex perience with BDD framework and worked on test automation using Python, Selenium , etc.
Experience in medical device or similar product development, design verification/validation, software integration , risk management, reliability engineering, process validation and Quality systems.
Deep domain knowledge in design verification and validation of medical devices is a plus.
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards.
Demonstrated experience in accomplishing objectives .
Able to deliver on multiple projects simultaneously.
Self-motivated with good interpersonal skills
Good team player to achieve team goals and guide junior team members in the team.
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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