Manufacturing Engineer-329
One Year Contract in Brooklyn Center MN Job Title:
Manufacturing Engineer-329 Job Duties:
Completes Design History File documentation Creates and delivers presentations throughout the organization Design of Experiments (DOE) and Statistical Process Control (SPC) Determines manufacturing operation requirements and process parameters Develops product and process improvements Supports manufacturing, development, and implementation processes Utilizes FMEA within process development ,Ensures compliance with GMP's Generates documentation for engineering protocols and reports This position is responsible for improving medical device manufacturing processes.
The Manufacturing Engineer interacts closely with the Operations team as well as several engineering disciplines such as Process Development, Test Engineering, Quality, and Reliability Engineers.
This position will understand the product performance and the effects of the manufacturing process on the product.
Position
Responsibilities:
Make use of appropriate quality tools, such as DOE, SPC, hypothesis testing, and capability studies; to measure, monitor, improve and control the mfg.
line and select processes.
Implement GMP (good manufacturing practices) to processes and share improvements across the site Utilize project management skills to drive continuous improvement initiatives to optimize yield, quality, cycle time and/or ergonomics.
Create written documents, test plans and reports that demonstrate technical rationale for associated decisions(s) (e.
g.
qualifications, risk assessments, and work instructions) Work with product development engineering to drive back lessons learned as new products are being developed.
Work with process development engineering in the evaluation of process FMEAs and failure analysis.
Basic
Qualifications:
Bachelor of Engineering, or related science Minimum of 2 yrs.
experience or MS degree Technical knowledge of manufacturing processes Demonstrated experience with computers using Microsoft Office (Word, Excel, PowerPoint).
Desired/Preferred
Qualifications:
Bachelors of Science/Engineering Proven ability to influence cross functionally to drive results.
Experience understanding proper documentation/quality requirements for a regulated environment Aptitude for quickly learning and assimilating a broad array of information Excellent data analysis skills and proficient in the use of statistical tools in problem solving Experience in medical product mfg.
/ assembly operations Experience in Lean Manufacturing / Six Sigma methodologies ISO 13485/GMP Experience Understanding of Development Protocols-IQ/OQ/PQ Experience interpreting mechanical drawings Experience conceiving and communicating mechanical design concepts to drafting team Experience improving manufacturing processes to improve yield and/or reduce scrap Click here to apply.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
Manufacturing Engineer-329 Job Duties:
Completes Design History File documentation Creates and delivers presentations throughout the organization Design of Experiments (DOE) and Statistical Process Control (SPC) Determines manufacturing operation requirements and process parameters Develops product and process improvements Supports manufacturing, development, and implementation processes Utilizes FMEA within process development ,Ensures compliance with GMP's Generates documentation for engineering protocols and reports This position is responsible for improving medical device manufacturing processes.
The Manufacturing Engineer interacts closely with the Operations team as well as several engineering disciplines such as Process Development, Test Engineering, Quality, and Reliability Engineers.
This position will understand the product performance and the effects of the manufacturing process on the product.
Position
Responsibilities:
Make use of appropriate quality tools, such as DOE, SPC, hypothesis testing, and capability studies; to measure, monitor, improve and control the mfg.
line and select processes.
Implement GMP (good manufacturing practices) to processes and share improvements across the site Utilize project management skills to drive continuous improvement initiatives to optimize yield, quality, cycle time and/or ergonomics.
Create written documents, test plans and reports that demonstrate technical rationale for associated decisions(s) (e.
g.
qualifications, risk assessments, and work instructions) Work with product development engineering to drive back lessons learned as new products are being developed.
Work with process development engineering in the evaluation of process FMEAs and failure analysis.
Basic
Qualifications:
Bachelor of Engineering, or related science Minimum of 2 yrs.
experience or MS degree Technical knowledge of manufacturing processes Demonstrated experience with computers using Microsoft Office (Word, Excel, PowerPoint).
Desired/Preferred
Qualifications:
Bachelors of Science/Engineering Proven ability to influence cross functionally to drive results.
Experience understanding proper documentation/quality requirements for a regulated environment Aptitude for quickly learning and assimilating a broad array of information Excellent data analysis skills and proficient in the use of statistical tools in problem solving Experience in medical product mfg.
/ assembly operations Experience in Lean Manufacturing / Six Sigma methodologies ISO 13485/GMP Experience Understanding of Development Protocols-IQ/OQ/PQ Experience interpreting mechanical drawings Experience conceiving and communicating mechanical design concepts to drafting team Experience improving manufacturing processes to improve yield and/or reduce scrap Click here to apply.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
