Principal Engineer, DS Process Development

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Company: JenaValve Technology

Location: Irvine, CA 92697

Description:

Description

Job Title: Principal Engineer, DS Process Development

  • Principal Engineer I, DS Process Development
  • Principal Engineer II, DS Process Development
  • Principal Engineer III, DS Process Development

Supervisor/Manager Title:Manager, DS Manufacturing

Job Description Summary:Responsible for process development and manufacturing engineering activities. Act as an interface between R&D, pilot, and commercial manufacturing.Contributes to the Delivery System product life cycle. Optimization and development of new or current manufacturing processes

Job Responsibilities:

  • Technical engineering support for delivery systems to ensure process and equipment are characterized and scaled by utilizing new technology and standard work.
  • Lead/support equipment, tooling, and fixture design for development and production activities.
  • Identify and implement manufacturing process improvements internally and at contract manufacturers.
  • Analyze and resolve complex manufacturing and compliance issues (CAPA, non-conformances, audit observations, etc.).
  • Lead short-term and long-term manufacturing process improvement activities.
  • Partner with Quality and R&D Engineers to develop and implement critical manufacturing processes.
  • Process development of manufacturing processes and validations (IQ/OQ/PQ) for new product introduction and continuous improvement.
  • Provide root cause analysis investigations and development/implement corrective actions for component and device nonconformance.
  • Managing key suppliers and working directly with contract manufacturers.
  • Provide technical support for design qualifications, design transfer, activities for regulatory submissions, product and process development and implementation of design control documents, and approval of product/process change.
  • Manage all manufacturing-related aspects of the project within a team.
  • Develop training and documentation materials (e.g., work instructions) for development and production activities.
  • Provide real time production line support.

Qualifications

Required Education and Experience:

  • A Bachelor of Science degree in Mechanical or Biomedical Engineering (or equivalent engineering degree) is required.
  • Minimum of 12+ years experience in Manufacturing or R&D Engineering is required with a preference in delivery systems or catheters.Level I, II, III DOE.
  • Must have experience in the use of CAD (SolidWorks) packages.
  • Knowledge of equipment qualification (IQ/OQ/PQ) and design verification (including statistical techniques used) in the medical device industry or other regulated industries is required.
  • Must have experience in designing and implementing fixturing from design concept to a clinical/commercial production line.
  • Must have experience in implementing equipment from parameter/settings origin to the production line.
  • Knowledge and experience in Work Instruction creation and implementation.

Skills and Abilities Required for This Job:

  • Must have experience in the use of CAD (SolidWorks) packages.
  • Must be able to work effectively and collaborate within cross-functional teams.
  • Must be able to effectively articulate (verbally and in writing) results and conclusions to technical and non-technical personnel.
  • Must have strong project management and documentation skills.
  • Must take initiative and have the ability to conduct hands-on work.
  • Must possess the ability to handle multiple tasks with high attention to detail.



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