Manufacturing Engineer I

Title: Manufacturing Engineer I

Location: Pomona, California

Duration: 12+ months

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.
  
  

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.
  
  

Consultants Eligible Benefits Upon Waiting Period

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)
  
  

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs..