Primary Function of Position:
Contribute your leadership and technical skills in the areas of manufacturing process technologies, problem-solving, training, and project management in a growing medical device company. In this key role, you will be the driving force behind Lean tool implementation and continuous improvement projects site-wide. Your combination of training, motivational skills, analytical problem-solving ability, and passion for Lean manufacturing will be just the right fit for the manufacturing environment of precision instruments for minimally invasive robotic surgery.
Roles & Responsibilities:
- Manufacturing responsibility for tooling/fixtures, manufacturing equipment, and design improvements in production.
- Evaluate and challenge mechanism designs for reliability, functionality, and manufacturability. Provide suggested change proposals.
- Approve design releases to manufacturing, review engineering documentation, and provide vendor and in-house DFM inputs.
- Review/approve and determine the impact of ECOs from manufacturing and field perspectives.
- Take responsibility for developing and maintaining compliance with the quality system.
- Evaluate and help in the selection of suppliers for mechanical parts if required. Help resolve supplier quality issues.
- Update and revise Manufacturing Process Instructions (MPIs) to ensure accuracy and completeness
- Address line support issues as they arise
- Document and report any variances, problems, issues, or concerns on all aspects of the manufacturing process
- Provide production personnel with expectations and performance feedback regularly in the production process
- Drive improvements in safety, quality, production, and cost
- Understand, train personnel, and enforce strict adherence to the applicable Department Operating Procedures (DOPs) and Standard Operating Procedures (SOPs) of the Quality System
- Maintain up-to-date and accessible training records for MPIs and Quality System documents
- Assist in setting and attaining quarterly and annual production goals
- Learn and enforce company safety policies and practices
- Review and disposition of discrepant material in the manufacturing line. Implement corrective actions to prevent recurrences.
- Active participant in quality improvement initiatives, providing feedback to find the root cause and problem-solving.
- Design and documentation responsibilities for custom and standard production tooling/fixtures.
- Process and part design/documentation duties for cost reduction programs.
kills, Experience, Education, & Training:
- BSME required.
- MSME preferred.
- Customs and material department knowledge preferred
- Strong communications skills across team organizations and cultures.
- Interface with shipping and receiving activities preferred.
- Mid/high volume complex mechanism manufacturing engineering experience preferred.
- Experienced in ISO 13485, or medical device manufacturing environment.
- Must be able to speak, read and write in English 85%.
- Must be able to travel to the USA
Intuitive es un empleador que brinda igualdad de oportunidades de empleo. Proporcionamos igualdad de oportunidades de empleo a todos los solicitantes y empleados cualificados, y prohibimos cualquier tipo de discriminación y acoso, independientemente de su raza, sexo, condición de embarazo, orientación sexual, identidad de género, origen nacional, color, edad, religión, condición de veterano protegido o de discapacidad, información genética o cualquier otra condición protegida por las leyes federales, estatales o locales aplicables.
