Eng I, V&V

Job Description

Eng I, V&VApply Now Save JobThis is where you save and sustain livesAt 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. Youll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.Baxters 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.About Baxter Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter s employees worldwide are building upon the company s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care. 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 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.
• 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 Bachelors Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field Overall 4 to 7 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 clearlyReasonable AccommodationsBaxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to hidden_email 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 .097139Apply Now Save Job,

Keyskills :
verificationvalidationtest casesproduct designdesign controlrisk managementquality systemstest procedurescomputer sciencepreventive action