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Automation Engineer
Job in
Indianapolis, Marion County, Indiana, 46262, USA
Listed on 2025-12-01
Listing for:
consultpharmatek
Full Time
position Listed on 2025-12-01
Job specializations:
-
Engineering
Systems Engineer
Job Description & How to Apply Below
Indianapolis, United States | Posted on 10/07/2024
- Industry Pharma/Biotech/Clinical Research
- Job Type Full time
- Work Experience 5+ years
- City Indianapolis
- State/Province Indiana
- Country United States
The scope of this role is to provide direct coordination and integrated Automation Support within Global Robotics Asset Portfolio to ensure the outputs required are developed and delivered,inclusive of delivery to sites in Indianapolis, Raleigh Durham NC, Concord NC,Alzey Germany, and potentially other future sites.
- Highlyversed in Allen Bradley Rockwell Controls including Studio
5000 and Factory Talk SE applications. (Required) - Experience with FANUC Robotic systems desired but not required
- Experience in Commissioning and Qualification, asset delivery, validation activities and cGMP regulations.
- Experience delivering and/or troubleshooting automated applications within the pharmaceutical industry.
- Workwith client Platform owner and Robotic application integration to troubleshoot, shakedown, and oversee Factory Acceptance Testing (FAT) andSite Acceptance Testing (SAT).
- Troubleshootsystem issues found during production and help identify and implement solutions.
- Evaluateproduction metrics and historian data to identify issues, recommend andhelp implement improvements.
- Abilityto travel to client production sites up to 25%+ (1-2 weeks per month asneeded by the project
- Demonstratedability to effectively work independently and to take initiativeespecially within a complex network environment
- Previousautomated assembly equipment validation experience
- Strong documentation management and technical writing skills
- Contribute to the completion of projects, manage own time on agreed targets, develop plans for own projects and leads small project teams
- Demonstrate good planning, organizing, time management and team participation skills
- Modifymoderately complex to highly complex control logic that requires a degreeof scientific and/or manufacturing process expertise
- Clearly communicate progress and issues to peers
- Mustbe willing to work onsite in Indianapolis, IN
- Mustbe willing to travel to multiple sites
- Musthave 5+ years of experience as an Automation Engineer (pharmaceuticalenvironment experience highly preferred)
- Bachelor’sDegree or equivalent required
- Proficiency using PC and Microsoft Office tools
- Outgoing personality with a strong ability to communicate effectively with peers inclear, concise terms
- Abilityto work as part of a team
- Strong problem-solving and critical thinking skills
- Excellent organizational and time management skills
- GMP/Validationpractices
- Intermediate skills with WORD (authoring/editing large technical documents with styles,tables, TOCs, track changes)
- Basic skills with EXCEL and Power Point
- Strong interpersonal skills and clear communication capabilities
- Experience with and tolerance for high levels of challenge and change
- Responsible for installing, maintaining, and troubleshooting automated utility,processing, filing, inspection, and packaging equipment
- Contributetechnical content to validation protocols on automation systems and perform execution of protocols
- Highly versed in Allen Bradley Rockwell Controls including Studio
5000 and Factory Talk SE applications.(Required) - Experience with FANUC Roboticsystems desired but not required
- Experience in Commissioning and Qualification, asset delivery, validation activities and cGMP regulations.
- Experience delivering and/ortroubleshooting automated applications within the Pharmaceutical industry.
- Work with client's Platform ownerand Robotic application integration to troubleshoot, shakedown, and oversee
Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT). - Troubleshoot system issuesfound during production and help identify and implement solutions.
- Evaluate production metrics and historian data to identify issues, recommend and help implement improvements.
- Ability to travel to client's production sites up to 25%+ (1-2 weeks per month as needed by the project
- Demonstrated ability to effectively work independently and to take initiative, especially within acomplex network environment
- Previous automated assemblyequipment validation experience
- Strong documentation management and technical writing skills
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