Overview
This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives
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Support for Parents
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Continuing Education/
Professional Development -
Employee Health &
Well-Being Benefits -
Paid Time Off
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2 Days a Year to Volunteer
Success Profile
What makes a successful Research and Development team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Courage
- Action Oriented
- Collaborates
- Cultivates Innovation
- Manages Ambiguity
- Drives Results
Eng II, V&V
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.
Position Overview
As System Verification and Validation (V&V) Test engineer for Infusion pumps team within Medication delivery business, the incumbent will have an independent responsibility of following instructions clearly in executing Test procedures for supporting all activities related to Design Verification of the medical devices. Candidate will also assist in maintaining Lab equipment, work with Design engineers to help build Test fixtures/assemblies and assisting with Lab logistics.
Essential Duties and Responsibilities
Lead/Execute, perform, summarize and report out verification test activities Medical devices: Which includes but not limited to:
- Understand URS (User requirements) / System Requirements and prepare the System Level Test cases and Prepare test procedures.
- Understand the product functionality and perform the Functional and Performance testing for the product.
- Lead/Support and perform all Design Verification activites
- Perform Installation/Operational/Performance Qualification Protocols
- Prepare Traceability Matrices and Final Reports.
- Support compliance/ closure of Regulatory and Quality requirements
- Follow Test instructions and Test protocols.
- Follow instructions clearly from Design engineers during Test execution.
- Support Design engineers in Test fixture creation, building up & tearing down Test equipment.
- Support Lab logistics and maintain the material supply for testing requirements. Support Calibration activities.
- Diagnose, isolate and investigate problem reports and defects.
- Support to work with external test houses (such as EMI, EMC tests for electrical boards and full device) to define the test scope, author the test plans, test procedures, execute & consolidate the reports
- Ensure good documentation and Good Manufacturing practices are followed in the Verification Process
- Experience in IEC basic safety, EMI-EMC standards
- Interacts with design team to resolve tests-related technical issues.
- Presents the findings / objective evidences 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.
Qualifications / Experience and/or Background
Bachelor's Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field Overall 5 to 8 yrs of experience with minimum 2 years in System Verification testing and performance testing. Hands on experience in overall final design verification/validation(V&V) testing of medical products. Relevant technical testing/reliability experience in electro-mechanical, electrical testing of Medical Devices. An understanding of test methods and processes as well as the methods used to verify product in the realms of; mechanical, electrical, functional testing environments. Basic 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. Understanding of hardware and software product design methodologies and test practices. Experience in medical device or similar product development, design verification/validation, system integration (hardware/Subsystem/Software), risk management, reliability engineering, process validation and Quality systems Basic understanding of and adherence to FDA,MDD/MDR, ISO and IEC design control procedures, regulations and standards. Self-motivated with good interpersonal skills. Ability to follow instructions clearly.
Preferred Candidates
- System V&V Engineers with Experience in Infusion pumps design verification testing.
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.
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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