This role focuses on developing validating and optimizing SMT manufacturing processes and equipment programs to ensure high yield throughput and adherence to quality standards. You will also lead continuous improvement initiatives perform root cause analysis for defects and support production through lean implementation DFM improvements and technical training
Requirements
- Bachelors of Science degree in an engineering discipline
- Experience with electronic/electro-mechanical products in a high-volume manufacturing environment.
- Knowledge and experience in GMP regulated environment requirements and preferably ISO-13485.
- Working knowledge in Lean Manufacturing DOE FMEA and SPC techniques.
- Experience with PCBA and/or FPCA assembly processing equipment programming and SMT technologies.
- Able to apply engineering principles to investigate analyze plan design develop validate and implement manufacturing processes and/or test stations
Benefits
Salary Package
Medical Device Industry Exposure
Required Skills:
SMT Process Engineering within the medical device industry.
Required Education:
Experience with electronic/electro-mechanical products in a high-volumemanufacturing environment. Knowledge and experience in GMP regulated environment requirements andpreferably ISO-13485. Working knowledge in Lean Manufacturing DOE FMEA and SPC techniques. Experience with PCBA and/or FPCA assembly processing equipment programmingand SMT technologies. Able to apply engineering principles to investigate analyze plan design developvalidate and implement manufacturing proces
This role focuses on developing validating and optimizing SMT manufacturing processes and equipment programs to ensure high yield throughput and adherence to quality standards. You will also lead continuous improvement initiatives perform root cause analysis for defects and support production throug...
This role focuses on developing validating and optimizing SMT manufacturing processes and equipment programs to ensure high yield throughput and adherence to quality standards. You will also lead continuous improvement initiatives perform root cause analysis for defects and support production through lean implementation DFM improvements and technical training
Requirements
- Bachelors of Science degree in an engineering discipline
- Experience with electronic/electro-mechanical products in a high-volume manufacturing environment.
- Knowledge and experience in GMP regulated environment requirements and preferably ISO-13485.
- Working knowledge in Lean Manufacturing DOE FMEA and SPC techniques.
- Experience with PCBA and/or FPCA assembly processing equipment programming and SMT technologies.
- Able to apply engineering principles to investigate analyze plan design develop validate and implement manufacturing processes and/or test stations
Benefits
Salary Package
Medical Device Industry Exposure
Required Skills:
SMT Process Engineering within the medical device industry.
Required Education:
Experience with electronic/electro-mechanical products in a high-volumemanufacturing environment. Knowledge and experience in GMP regulated environment requirements andpreferably ISO-13485. Working knowledge in Lean Manufacturing DOE FMEA and SPC techniques. Experience with PCBA and/or FPCA assembly processing equipment programmingand SMT technologies. Able to apply engineering principles to investigate analyze plan design developvalidate and implement manufacturing proces
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