at Rose International Inc. in Cary, Illinois, United States
Job Description
Date Posted: 06/05/2024
Hiring Organization: Rose International
Position Number: 465328
Job Title: Manufacturing Engineer
Job Location: Cary, IL, USA, 60013
Work Model: Onsite
Shift: 8:00am to 5:00pm, M-F
Employment Type: Temporary
Estimated Duration (In months): 19
Min Hourly Rate($): 50.00
Max Hourly Rate($): 54.00
Must Have Skills/Attributes: Assembly, Manufacturing Engineer, Medical device
**Only those lawfully authorized to work in the designated country associated with the position will be considered.**
**Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Qualifications:
• A degree or equivalent and a minimum of 2 or more years of experience.
• Professional mastery of a specialized field of expertise that typically requires a college degree or equivalent.
• Professional knowledge gained through substantial applicable work experience, to supplement formal knowledge, in order to apply principles and concepts of own subject/technical discipline in resolving issues as they arrive.
• Attention to detail in making evaluative judgements based on the analysis of factual information.
This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. The Manufacturing Engineer will provide technical and engineering support to implement a new high speed, automated medical device assembly line. This is a significant investment in our site, and critical to achieve our business goals.
Responsibilities include:
• Support the installation, validation and production ramp up of a custom automation line for the high-volume manufacture of medical devices.
• Provide technical, engineering, validation and documentation support.
• Support engineering and project management in FAT, installation, and commissioning of the new assembly line.
• Support development of the process FMEA and control plan for the new assembly process.
• Complete process validations including VP, URS, IQ, OQ, PQ and associated documentation.
• Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP).
• Collaborate with product and manufacturing engineering, equipment vendors, maintenance technicians and operations leadership to troubleshoot process and equipment issues.
• Support line performance monitoring and lead practical problem solving (PPS) projects to remediate systemic issues.
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
