Overview
On Site
$Based on experience
Accepts corp to corp applications
Contract - Independent
Contract - W2
Contract - 11 month(s)
Skills
Research and Development
Cross-functional team
Product development
IT consulting
Real-time
Medical devices
Design controls
Feasibility study
Design documentation
Mechanical engineering
Materials science
Biomedical engineering
Critical thinking
Agile
SAP BASIS
Leadership
Collaboration
DFSS
Design
Analytical skill
Manufacturing
Operations
Filing
Testing
SolidWorks
Management
Marketing
Sales
Documentation
Job Details
Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly
to match skill supply and demand on a real-time basis.
to match skill supply and demand on a real-time basis.
Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent. We have a stellar reputation for striving to achieve high ethical standards. Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business.
TITLE:Engr 3, Product Development
LOCATION:La Brea CA
Job Description:
Lead R&D deliverables throughout the medical device design control process for intravenous infusion sets and connection devices
Collaborate within a cross-functional team to plan, develop, modify, implement, and support IPD products through the application of rigorous engineering practices
Engineer robust products through strong understanding and application of engineering fundamentals and DFSS principles.
Develop technical plans and guide the team to develop design inputs, conduct analytical and empirical feasibility studies, refine product configurations and designs, verify and validate subsystems and systems, concurrently transfer designs alongside Manufacturing and Operations, and provide design documentation to support global Regulatory filing strategies
Execute design verification testing to confirm design outputs meet design input requirements.
Required Qualifications:
BS Mechanical Engineering, Materials Engineering or Biomedical Engineering
Work experience 5 years or 3 years plus an advanced degree
Critical thinking able to work with moderate guidance in own area of knowledge.
SolidWorks or equivalent CAD tool
Ability to manage multiple projects of varying scopes in parallel
Ability to work leading or as part of a cross-functional team with members from marketing, sales, clinical, regulatory, medical affairs, quality, manufacturing, etc.
Experience with medical device design control processes and creating and maintaining design control documentation.
Lead R&D deliverables throughout the medical device design control process for intravenous infusion sets and connection devices
Collaborate within a cross-functional team to plan, develop, modify, implement, and support IPD products through the application of rigorous engineering practices
Engineer robust products through strong understanding and application of engineering fundamentals and DFSS principles.
Develop technical plans and guide the team to develop design inputs, conduct analytical and empirical feasibility studies, refine product configurations and designs, verify and validate subsystems and systems, concurrently transfer designs alongside Manufacturing and Operations, and provide design documentation to support global Regulatory filing strategies
Execute design verification testing to confirm design outputs meet design input requirements.
Required Qualifications:
BS Mechanical Engineering, Materials Engineering or Biomedical Engineering
Work experience 5 years or 3 years plus an advanced degree
Critical thinking able to work with moderate guidance in own area of knowledge.
SolidWorks or equivalent CAD tool
Ability to manage multiple projects of varying scopes in parallel
Ability to work leading or as part of a cross-functional team with members from marketing, sales, clinical, regulatory, medical affairs, quality, manufacturing, etc.
Experience with medical device design control processes and creating and maintaining design control documentation.