Senior R&D Engineer (Front End)-00000KSI
Description
ROLES & RESPONSIBILITIES
- Policies: Know & follow J&J policies & procedures related to work activities performed in area of responsibility
- Safety: Follow all company safety policies & other safety precautions within work area. Promote safety to all associates that enter work area
- Monitoring healthcare environment, includes government & regulatory policy; understand company global and local business strategy
- Lead market study to gain customer insights via desktop research, immersion and interview with customers such as surgeons etc. execute specific & general assignments that establish the feasibility of innovative
- Work one-on-one with customer stakeholders to identify the alignment
- Interpret customer & marketing input to define their potential clinical & business needs
- Responsible for the investigation of the key stakeholder on the way of questionnaire JOC (jobs, outcomes & constraints) etc
- Utilize JOC and VOC (voice of customer) methodologies & surgical procedure knowledge to define product & design options
- Lead cross functional assessment: IP, Regulatory, Supply Chain, Technique, HE&R
- Lead ideation workshop for product concept generation
- Responsible for project management: planning and drive execution, key stakeholders alignment, cross functional team engagement, and customer Relationship Management
- Contribute to innovative product, system & component design solutions
- Contribute to and support wet lab and pre-clinical model design
- Perform detailed design analysis & provide input or approval for detailed design specifications
- Provide support to patent attorneys for patent filing
- Assist in developing & monitoring project plan, budget, contingency plans & work estimation
- Coordinate integration of complex sub-system product designs
- Learn medical terminology, procedures & instrumentation
- Provide peer feedback & may mentor junior associates as required
Technical (Biomedical1): Design and evaluate prototype with related in vivo, in vitro model and with customers; Optimize the prototype based on the feedback from customers. Perform tests against internal and external specification or standards; understand the key process parameters to scale up from prototypes to mass production
Qualifications
Qualifications
- Education / Degree Required:
Bachelor of Medicine, Or Master of Medicine Degree (Surgery discipline is preferred) Or Bachelor of Science, or Master of Science with rich front end experience for medical device
- Skill Sets 1:
- High ethics reflecting Credo values
- Bilingual: English/Mandarin required
- Excellent communication skills
- Literature study and analytic capability
- Basic knowledge & understanding of medical regulatory requirements
- Effective oral, written, & presentation communications in English/Mandarin
- Technical writing: protocols, testing results, procedures, status & special reports
- Project management skills
- Leadership skills
- Knowledge & understanding of medical regulations & their impact on business, ISO (International Organization for Standardization) & GMP (Good Manufacturing Practices)
- Information & risk analysis skills
- Quality, statistical process controls
- Knowledge of part manufacturing processes & tooling methodologies
- Effective team interpersonal skills and the ability to work effectively within diverse cultural environments
- Conflict analysis & resolution
- Consulting, design review, & constructive feedback
- Negotiating (e.g., internal & external customers)
- Networking and interaction
- Team building
- Able to work efficiently & effectively in an ambiguous environment
- Able to adapt to shifting priorities
- Able to handle rapid pace environment
- Able to take initiative & be self-managing
- Patent interpretation
- Knowledge of commercial execution
- Computer Skills 1:
- Personal computer software – Windows: word processing, project planning, presentation, e-mail & spreadsheet software
- Special design analysis software, (e.g., FEA, mold flow)
- Internet search skills
J2W: LI ASPAC
Primary Location:Asia Pacific-China-Jiangsu-Suzhou
Organization: Johnson & Johnson Medical Suzhou Ltd. (7054)
Travel:Yes, 10 % of the Time
Job Function: Biomedical Engineering
Description
ROLES & RESPONSIBILITIES
- Policies: Know & follow J&J policies & procedures related to work activities performed in area of responsibility
- Safety: Follow all company safety policies & other safety precautions within work area. Promote safety to all associates that enter work area
- Monitoring healthcare environment, includes government & regulatory policy; understand company global and local business strategy
- Lead market study to gain customer insights via desktop research, immersion and interview with customers such as surgeons etc. execute specific & general assignments that establish the feasibility of innovative
- Work one-on-one with customer stakeholders to identify the alignment
- Interpret customer & marketing input to define their potential clinical & business needs
- Responsible for the investigation of the key stakeholder on the way of questionnaire JOC (jobs, outcomes & constraints) etc
- Utilize JOC and VOC (voice of customer) methodologies & surgical procedure knowledge to define product & design options
- Lead cross functional assessment: IP, Regulatory, Supply Chain, Technique, HE&R
- Lead ideation workshop for product concept generation
- Responsible for project management: planning and drive execution, key stakeholders alignment, cross functional team engagement, and customer Relationship Management
- Contribute to innovative product, system & component design solutions
- Contribute to and support wet lab and pre-clinical model design
- Perform detailed design analysis & provide input or approval for detailed design specifications
- Provide support to patent attorneys for patent filing
- Assist in developing & monitoring project plan, budget, contingency plans & work estimation
- Coordinate integration of complex sub-system product designs
- Learn medical terminology, procedures & instrumentation
- Provide peer feedback & may mentor junior associates as required
Technical (Biomedical
Qualifications
Qualifications
- Education / Degree Required:
Bachelor of Medicine, Or Master of Medicine Degree (Surgery discipline is preferred) Or Bachelor of Science, or Master of Science with rich front end experience for medical device
- Skill Sets
- High ethics reflecting Credo values
- Bilingual: English/Mandarin required
- Excellent communication skills
- Literature study and analytic capability
- Basic knowledge & understanding of medical regulatory requirements
- Effective oral, written, & presentation communications in English/Mandarin
- Technical writing: protocols, testing results, procedures, status & special reports
- Project management skills
- Leadership skills
- Knowledge & understanding of medical regulations & their impact on business, ISO (International Organization for Standardization) & GMP (Good Manufacturing Practices)
- Information & risk analysis skills
- Quality, statistical process controls
- Knowledge of part manufacturing processes & tooling methodologies
- Effective team interpersonal skills and the ability to work effectively within diverse cultural environments
- Conflict analysis & resolution
- Consulting, design review, & constructive feedback
- Negotiating (e.g., internal & external customers)
- Networking and interaction
- Team building
- Able to work efficiently & effectively in an ambiguous environment
- Able to adapt to shifting priorities
- Able to handle rapid pace environment
- Able to take initiative & be self-managing
- Patent interpretation
- Knowledge of commercial execution
- Computer Skills
- Personal computer software – Windows: word processing, project planning, presentation, e-mail & spreadsheet software
- Special design analysis software, (e.g., FEA, mold flow)
- Internet search skills
J2W: LI ASPAC
Primary Location:Asia Pacific-China-Jiangsu-Suzhou
Organization: Johnson & Johnson Medical Suzhou Ltd. (7054)
Travel:Yes, 10 % of the Time
Job Function: Biomedical Engineering