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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.
Job Responsibility:
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
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
Requirements:
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
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
Nice to have:
System V&V Engineers with Experience in Infusion pumps design verification testing