Sr Engineer AFP

Location: Thousand Oaks, CA
Date Posted: 09-13-2017
Day to Day Responsibilities:            
Provide sustaining support by offering technical support; troubleshooting and resolving production problems related to electro-mechanical design. Interact with manufacturing operations, quality and supply chain personnel to define and solve manufacturing/design issues and/or design improvements.
 
Summary:
Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Systems/Software Engineering background need apply and will be considered!!!
Sustaining and developing drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate needs to ensure successful device development of these mechanical and electro-mechanical medical devices. The Sr. Engineer will work closely with team members to develop detailed engineering specifications, device design & development, support verification, validation, and regulatory submissions of these devices. The role of the Sr. Engineer is to work within a cross-functional organization to utilize technologies and methodologies that support short-cycle robust device development.
 
Responsibilities:
  • Work cross-functionally with individuals and project teams in Marketing, Operations, and Development
  • Create and assess product requirements to determine technical coverage and proper integration different subsystems.
  • Create and execute to project plans and schedules
  • Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects.
  • Provide deep technical assistance for junior engineers.
Skills:
  • BS in Engineering and previous experience in a medical device industry
  • Led projects from development through the 510k and PMA approval process.
  • Strong background in engineering and commercialization of electro-mechanical medical devices.
  • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
  • Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510k) submissions.
  • Experience in drug/device combination product design and development
Familiar with the following standards:
  • Quality System Regulation 21CFR820
  • Risk Management ISO 14971
  • EU Medical Device requirements
  • Council Directive 93/42/EEC
  • Medical Electrical Equipment EN 60601
  • Small scale device assembly experience.
  • Ability to read, analyzes, and interprets general business periodicals, professional journals, technical procedures, or governmental regulations.
  • Strong problem solving, risk assessment, and risk management skills.
  • Must be capable of working on multiple projects in a deadline driven environment.

"This posting is for Contingent Worker, not an FTE"
 
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