R&D Engineer II at Boston Scientific Corporation Malaysia
Galway, Connacht, Ireland -
Full Time


Start Date

Immediate

Expiry Date

02 Jan, 26

Salary

0.0

Posted On

04 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

R&D, Product Design, Design Control, Documentation, Verification Testing, Validation Testing, Problem Solving, Communication, Leadership, Analytical Testing, Regulatory Compliance, Team Collaboration, Project Management, Patient Safety, Quality Assurance, Technical Guidance

Industry

Medical Equipment Manufacturing

Description
Responsible for supporting the development and commercialization of next-generation minimally invasive medical devices for the treatment of coronary artery disease. Participate and contribute to project teams, which typically includes the following activities: product design and development, product design troubleshooting and investigation support, report preparation. Demonstrates thorough knowledge of design control through generation of high-quality deliverables. Responsible for generation of design related documentation including prints, BOM's and specifications and driving their approval through documentation control processes. Work cross-functionally with project management, quality, manufacturing, regulatory, clinical, marketing, and others as required to ensure project success. Uses design change process to ensure proposed design changes are systematically and thoroughly analyzed, tested or rationalised and documented prior to implementation. Designs and coordinates design verification and validation testing. Summarizes, analyses, draws conclusions from and documents test results. Work closely with mechanical and analytical test laboratory supporting analytical testing and test method validations. Uses structured problem-solving techniques to investigate test failures. Support educational and marketing activities to promote the understanding and appropriate use of our products by our customers. Interfaces with vendors where projects require. Provide technical guidance within a team and be an effective communicator within a multidisciplinary and international organisation. Works independently to plan and schedule own activities necessary to meet timelines. Uses initiative to scope and execute tasks and activities by seeking out available data and expertise. May train and/or provide work direction to technicians and interns. Demonstrates a primary commitment to patient safety and product quality. HETAC Level 8 Degree in a relevant Technical Discipline, preferably Mechanical, Polymer, Materials or Biomedical Engineering. Strong R&D/technical experience preferably in the health care industry, minimum 3 years. Proven ability to work within a regulated industry environment and with a track record of accomplishments. Self-starter with the ability to work independently to plan, schedule and execute activities necessary to meet project timelines to schedule. Excellent interpersonal and communication skills with good leadership abilities. Excellent analytical and problem-solving skills.
Responsibilities
The R&D Engineer II is responsible for supporting the development and commercialization of minimally invasive medical devices. This includes product design, troubleshooting, documentation, and cross-functional collaboration to ensure project success.
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