Eng Ii, V&v - Bengaluru, Karnataka, India - BAXTER
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.
Position Overview
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 testsrelated 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.
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.
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.
- System V&V Engineers with Experience
in Infusion pumps design verification testing.
Reasonable Accommodations
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.
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