Engineer

2 weeks ago

Pasir Ris, Singapore Fong’s Engineering & Manufacturing Pte Ltd Full time

**Engineer, Test ( SG ENDOSCOPY PTE LTD)**

**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
- Degree or Masters in Microbiology or related field
- Minimum 3-5 years relevant experience, preferably in Medical Device, Automotive or Aerospace

industry.
- Preferably 1-2 years of relevant experience in design verification and validation of Medical

Device or other highly regulated industries

**SKILLS**
- In-depth knowledge of test and design verification methodologies, regulatory

standards/environment requirements and required documentations.
- Good understanding of DOE (Design of Experiments) principles.
- Good command of Minitab or other statistical analysis software
- Excellent problem-solving and debugging skills.
- Proficiency in test automation tools and scripting languages
- Have good understanding of cybersecurity requirements for medical device testing.
- Good time management skills, including the ability to prioritize work and meet deadlines.
- Strong interdisciplinary communication skills with internal and external stakeholders

(customers, project, development, quality, and regulatory teams).

If you are looking for challenges and have the qualities and experience to undertake this challenging

experience, present and expected salary, and notice period.

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