Automation Engineer

Job Summary – Automation Engineer
• Support installation, testing and qualification of new equipment and equipment projects
• Provide on-site support  for equipment debug, testing & qualification
• Performs engineering tests, checkouts, and development engineering tasks
• Analyzes engineering test results and implements changes to resolve problems.
• Collects data, analyzes results and implements procedures
• Document equipment issues and propose solutions
• Development of preventative and predictive maintenance procedures
• Use of problem-solving techniques to address issues with machines and processes
• Experience in a technology-based industry, where automated assembly techniques are utilized
• Knowledge of automated equipment systems and tools - robotics, vision, material handling, Conveyors, PLC, HMI, Pick-Place-Pack, Inspection/Test

The experience we’re looking to add to our team:
• Engineering degree in related field or equivalent experience and training
• Minimum of 2 years of experience with Automation and Controls

Essential Responsibilities  • Provide support to the engineering and manufacturing, and quality functions within a team participation setting.
• Document and communicate the results of problem solutions and conduct analytical examinations to both internal and external customers.
• Responsible for implementing the document workflow process as a formal written procedure
• Advocate the usage of quality improvement and control tools.
• Update and develop documents where required including  technical manuals, instruction manuals, and other pertinent documents as part of an overall document plan to ISO 13485 requirements. 

Qualifications/Requirements  •     B.S in Engineering or Technical Practice.
• knowledge of Pharmaceutical/Medical device regulations of FDA - 21 CFR Part 11, 21 CFR Part 58, 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820.
• Minimum of 3 years of experience in an engineering or quality related position.
• Implementation experience with Medial Device ISO13485 IQ, OQ, and PQ protocol development and execution.
• Ability to develop and execute standard operating procedures that could consist of, Testing Methods, Safety Methods, and Manufacturing Methods. 
• Proficient in Microsoft Applications, word, excel ect..

Desired Characteristics  • Strong oral and written communication skills
• Capability to work in teams
• Six Sigma Green Belt Certified. 
• QMS implementation experience.
• Manufacturing Experience with Medical Industry Components

Qualification:

The experience we’re looking to add to our team:
• Engineering degree in related field or equivalent experience and training
• Minimum of 2 years of experience with Automation and Controls
 

Skill key word:

Robotics and Controls including programming of PLCs or IPCs
• Skilled in using PLC programs.

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