JOB RESPONSIBILITIES
· Develops and conducts test plans and protocols for design verification, process characterization, process validation, finished product and benchmarking study to generate test reports with sound engineering principle.
· Design, develop, and implement automated and manual test procedures for functional, performance, and regression testing.
· Identifies and consolidates requirement lists from product performance, functional and regulatory aspects
· Drives the entire design verification and validation activities to ensure compliance to regulatory requirements such as IEC, FDA, GMP, ISO and IEC standards.
· Develops and executes various benchmark testing to understand product quality compared to existing products
· Develops and validates new equipment and fixtures to conduct various testing.
· Conducts feasibility testing together with product development and quality team
· Liaise with external test labs to obtain critical data for test reports.
· Work with equipment vendors to identify test equipment that meets testing requirements.
· Participate in Risk Management and Failure Analysis exercises such as FMEA (Failure Mode & Effects Analysis).
· Identify, document, and track defects using issue tracking tools.
· Work closely with development teams to identify and address potential issues early in the development lifecycle
· Communicate all identified risks to your Test/Team Lead
· Summarizes test report and present to project and management team.
· Perform other tasks as assigned by the supervisor.
JOB REQUIREMENTS
· Degree or Masters in Mechanical/Electrical/Bio Engineering or related field
EXPERIENCE
· Minimum 3-5 years relevant experience, preferably in Medical Device, Automotive or Aerospace industry.
· Knowledge and familiar with IEC60601 test and requirements.
SKILLS
· Strong in mechanical and electrical fundamentals.
· Good understanding of DOE (Design of Experiments) principles.
· Prefarably with six sigma green belt training