Sr Eng, Verification
5 months ago
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) Sr.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 leading/supporting all activities related to Design Verification of the medical devices. Candidate will also will be responsible in maintaining Lab equipment, work with Design engineers to help build Test fixtures/assemblies and assisting with overall Lab logistics.
Essential Duties and Responsibilities
Lead/Execute, perform, summarize, and report out System 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 Design Verification activites Drive/Perform Installation/Operational/Performance Qualification Protocols Prepare Traceability Matrices and Final Reports. Lead compliance/ closure of Regulatory and Quality requirements Develop 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. Plan Lab logistics and maintain the material supply for testing requirements. 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 6 to 10 yrs of experience with minimum 3 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.Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.
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