Manufacturing Engineer I

Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Jigar Kachhia at email address    can be reached on #

630-576-1904

.
 
 
We have Contract role Manufacturing Process Development Engineer for our client at Pomona CA. Please let me know if you or any of your friends would be interested in this position.
 
Position Details:
Manufacturing Process Development Engineer- Pomona CA
Location                             : Pomona CA 91767
Project Duration                 : 11+ Months Contract
Pay                                : $25/hr. on W2
 
 
Job Summary:
Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
 
The position of Manufacturing Engineer I is within our CMI Unit located in Pomona, California.  This role will provide support for automated manufacturing process equipment including troubleshooting equipment issues, equipment modification, failure analysis, etc. for the Abbott manufacturing environment.  Develops, implements and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies and final assemblies.  Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost, determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. Acts as liaison between area owners and vendors for scheduled/unscheduled maintenance and calibration. Addresses any nonconformances as a result of environmental excursions (related to temperature and humidity) within validated rooms and equipment.
This job description will be reviewed periodically and is subject to change by management.
 
RESPONSIBILITIES:
•     Applies basic understanding of FDA, ISO and cGMP theories and principles.
•     Contribute to Group’s objectives by carrying out assignments.
•     Supports current automated manufacturing equipment, supporting a 24x7 production schedule.
•     Ability to investigate and modify existing control systems and user interfaces
•     Ability to investigate and modify existing vision inspection applications (Cognex), cameras and lighting
•     Write manufacturing work instructions, validation protocols and equipment specifications.
•     Supports Lean/Six Sigma Initiatives.
•     Supports design of experiments to improve understanding of impact of variability in manufacturing on downstream processes and aid in the development of improved manufacturing procedures and processes.
•     Supports the use of process mapping tools and manufacturing data to drive improvements in operational efficiencies and cost improvement initiatives.
•     Use of project management including vendor and interdepartmental interactions
•     Carries out duties in compliance with established business policies.
•     Demonstrates commitment to the development, implementation and effectiveness of Abbott Quality Management System per ISO, FDA, and other regulatory agencies.
•     Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
•     Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
•     May work with hazardous materials.
•     Perform other duties & projects as assigned.
 
MINIMUM QUALIFICATIONS | EDUCATION/EXPERIENCE:
•     BS degree in engineering or related field.
•     0-2 years of experience in engineering role.
•     Experience with computer applications include SolidWorks, AutoCAD, MS Word, Excel and Project.  
•     Verbal and written communication skills; Organized and detail oriented.
•     Ability to use MS Office and other manufacturing systems.
 
PREFERRED QUALIFICATIONS:
•     Basic knowledge of federal and other regulations governing medical device assembly and design, e.g. GMP, QSR, ISO and CMDR.
•     Understanding of machine function, mechanical/electrical or software engineering.
•     Knowledge of Lab View, PLC and other specialty machine and vision software.
•     Able to work with a variety of people on multiple projects; Ability to work independently and in a team environment.
•     Organized and detail oriented
•     Knowledge of structured problem-solving/lean tools.
 
COMPETENCIES:
•     Acts ethically and takes accountability for achieving outcomes.
•     Team work
•     Proactively listens to internal/external customers and clarifies expectations
•     Promptly and effectively handles issues and problems
 
 
 
To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Jigar Kachhia at email address    can be reached on #

630-576-1904

.
 
About generis tek: generis tek is a boutique it/professional staffing based in Chicago land. We offer both contingent labor & permanent placement services to several fortune 500 clients nationwide. Our philosophy is based on delivering long-term value and build lasting relationships with our clients, consultants and employees. Our fundamental success lies in understanding our clients’ specific needs and working very closely with our consultants to create a right fit for both sides. We aspire to be our client has most trusted business partner.