Principal Engineer, DS Process Development
Apply NowCompany: 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.