Engineer, II Verification & Validation
Baxter International · Bengaluru · onsite · Posted 5d ago
Undisclosed3–7 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Summary
Your Role at Baxter
What youll be doing
What youll bring
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
This is where your work makes a difference.
At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job-you will find purpose and pride.
Your Role at Baxter
The role of Verification Validation Engineer II is to independently Verify and Validating the device with minimal / no supervision. In addition to providing technical support and service in these areas, the incumbent may also perform the following functions: requisitioning, defining, initiating, specifying, documenting and training.
This position is based out of Bangalore and reporting to the VV Manager for PSS/GSS unit of HST.
What youll be doing
- Author, Execute, perform, summarize, report out verification validation test activities of components to a full system device: Which includes but not limited to:
- Test Plans, Test Procedures, User and Functional Requirements testing,
- Installation / Operational / Performance Qualification Protocols,
- Support compliance/ closure of Regulatory and Quality requirements before completing Design Outputs/ Program Deliverables.
- Support the qualification of lab area, productivity improvement efforts, including testing, building fixtures, calibration and data collection.
- Diagnose, isolate and investigate problem reports. Drive product improvements and/or bug fixes.
- Works with external test houses (such as EMI (Electromagnetic Interference), EMC (Electromagnetic Compatibility) 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 and Validation Process
- Participate in continuous improvement activities by supporting the implementation of process and product quality improvement initiatives
- Participate in Verification and Validation development process improvement and test automation.
- Maintains awareness of current regulatory trends and their impact on the Verification and validation status of equipment and processes.
- Support the SMEs on Regulatory responses and Audits, as needed
- Adheres to Baxter Quality Management system supports the quality audits.
- Presents the findings / objective evidence 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.
What youll bring
- Bachelors Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
- 3 to 7 years of experience in Verification and validation testing of Software, hardware and System.
- Relevant technical testing/reliability experience in electro-mechanical, electrical, or software testing
- An understanding of test methods and processes as well as the methods used to verify product in the realms of; software, mechanical, electrical, functional and environmental testing environments.
- Experience in - writing system, subsystem-level and module level verification and validation plans, procedures, Test Execution and Test report generation
- Understanding of hardware and software product design methodologies and test practices.
- Familiarity with reliability theory and analysis as it pertains to test quantities derived from reliability.
- Experience in medical device or similar product development, design verification/validation, system integration (involving software hardware), risk management, reliability engineering, process validation and Quality systems
- Deep domain knowledge in design verification and validation of medical devices is a plus
- Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards.
- Demonstrated experience in accomplishing objectives. Able to deliver on multiple projects simultaneously
- Self-motivated with good interpersonal skills
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
Automationprocess validationauditsDesign VerificationProcess ImprovementfixturesIndustrial Engineeringelectrical engineeringMechanical EngineeringHealthcareData CollectionMedical DevicesManufacturingoperationscompliance
About Baxter International
Baxter International
Healthcare
5k+
employees
1931
95 years old
Kolkata, West Bengal
India
₹20.4L PA avg
Avg at Baxter International
About
Baxter hires a range of talented and driven individuals with diverse skill sets and backgrounds, from scientists and researchers to industry professionals in manufacturing, engineering and technology,
Industries
HealthcareMedical EquipmentPharma
Employee ratings
10 reviews
3.8/ 5
Culture
3.9
Career growth
2.1
Work-life
3.5
Employees rate it well for
Work-Life Balance40Company Culture38
Find them on