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A Division
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GMP
Publications
& FDA.COM
"The GxP Family of
Quality Business"




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"We stand on a higher pillar of excellence!"
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Title |
Location |
Type |
Rate |
Apply |
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Design Engineer |
West
Chester PA |
Perm/Full |
$65,000 - $80,000 |
Submit |
Design Engineer
Overview:
Responsible for the design, development,
documentation, and process validation of
implants, instruments and other projects.
Responsible for managing multiple projects to
ensure on-time completion of deliverables. Also,
for gathering and implementing end user survey
information to achieve improved product design
and durability.
Responsibilities:
• Organize and proactively promote multiple
development projects and redesign projects in
support of on-time new product releases.
• Work from verbal, sketched and printed
documentation input.
• Ensure on-time execution of all project
deliverables, including specifications, layouts,
conceptual models, detailed designs, and
preliminary and final drawings.
• Perform and facilitate design and development
of product based on functional requirements,
operating technique and other provided or
developed specifications.
• Through design, apply new technology and
materials while reducing costs, improving
manufacturability, and assuring quality.
• Facilitate and execute prototype development
for projects, ensuring that customer review is
performed and documented.
• Communicate design and project status
information to Product Development, Purchasing,
Quality Assurance, Regulatory, vendors and
management, and Engineering Services.
• Present periodic project status reports.
• Know and follow all laws and policies that
apply to one's job, and maintain the highest
levels of professionalism, ethics and compliance
at all times.
• Diligently participate in our compliance
program-related activities as denoted by your
supervisor or our Chief Compliance Officer.
• Perform other assignments as needed.
Qualifications:
• Associates degree in Mechanical Engineering or
Engineering Drafting and Design.
• Three years minimum CAD solid modeling and
drafting experience.
• Medical device experience highly desirable.
• Proficient in Pro-Engineer version 2001 or
newer.
• Demonstrate ability to prioritize, organize
and manage multiple tasks.
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