Eng, Verification
Baxter International
This listing was originally posted on Baxter International's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
Upgrade to Pro to access the AI-generated 'Read before applying' briefing and other premium pharma intelligence.
Upgrade to Pro — $25/moThis 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. It was our founding belief in 1931 and continues to be our guiding principle. 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.
JOB SUMMARY:
Perform requirement analysis, verifiability of requirements and Conduct design verification and validation (V&V) activities for products being developed for upcoming Hill-Rom products, as well as for updates to existing products.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
· Work closely with System Engineer and other development engineers in reviewing Design inputs / specifications for verifiability.
· Collaborates with System Engineer and own the development of verification plan, verification protocols and scripts based on Design Inputs.
· Develop accurate schedules and estimate overall System V&V schedule.
· Develop testing tools, when required, to execute V&V.
· Execute test scripts to ensure design output meets design input, identify design defects during verification.
· Create defect logs and support in defect management.
· Maintain traceability of Design Inputs to Design Verification.
· Develop and maintain required Design History Files relating to test records, results, and issue observations.
· Complete all applicable trainings and comply with applicable Quality System documents.
· Applies new technical tools and concepts under the direction of others.
· Documents status and results accurately and succinctly, and with purpose.
· Seeks input from more experienced individuals to improve quality of deliverables
· Other duties may be assigned.
EDUCATION AND EXPERIENCE:
· Bachelor or master’s degree in one of the following areas: Mechanical Engineering / Electronics Engineering, or equivalent field with strong analytical thinking.
· 5 years of experience in product verification / validation, electrical module testing, software / firmware testing.
QUALIFICATIONS AND SKILLS:
· Knowledge in Lab Instrumentation.
· Candidates shall have hands on experience with measuring & test equipment such as Data loggers, Oscilloscopes, Force gage, Load cells, Pressure sensors, Flow sensors, Pressure regulators/gauges, Calipers, Multimeter, Thermocouples and Strain gauges.
· The candidate shall have capability to set up and configure the test system.
· The candidate shall possess the capability to perform data analysis and write test reports.
· Knowledge of using statistical software to analyze and graph data will be an added advantage.
· Good verbal and written communication skill in Chinese and English.
· The candidate shall be capable of working independently
· The candidate shall be capable of setting priorities and do multi-tasking.
· Familiarity with FDA’s Good Documentation Practice
· Previous experience with Medical Devices is added advantage
· Knowledge of Medical device product development process
· Other Competencies: Result Oriented, Commitment to Continuous Improvement and Effective Teamwork
· Strong organization and communication skills.
· Proficient problem solving.
· Adaptable to change
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here 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.
Explore related positions you might be interested in
We'll notify you when matching roles are posted.
Interviewed at Baxter International?
Help others prepare — share your experience anonymously.
MEDICAL DEVICES
Upgrade to Pro to access AI interview prep brief and other premium pharma intelligence.
Upgrade to Pro — $25/mo