Automation Engineer

SimoTech

Indianapolis, Indiana

JOB DETAILS
SKILLS
Automation, Automation Engineering, Biology, Biotech and Pharmaceutical, Capital Project, Code Reviews, Code of Federal Regulations, Communication Skills, Computer Science, Computer Systems, DeltaV, Drug Manufacturing, GMP (Good Manufacturing Practices), Industry Standards, Information Technology & Information Systems, Mentoring, Process Engineering, Regulations, Regulatory Requirements, Source Code/Configuration Management (SCM), System Integration (SI), System Validation, Team Player, Testing
LOCATION
Indianapolis, Indiana
POSTED
4 days ago

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Why SimoTech <\/span> <\/span> <\/span> <\/b>
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What is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust <\/span> , and excellence, we play a critical partnering role to our clients’ life -changing supply of products <\/span> t <\/span> <\/span> o patients. In return, there is an excellent salary, benefits, career progression, educational support and much more. <\/span> <\/span>
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Automation Engineer <\/span> <\/span> <\/span> <\/b>
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We are actively expanding our US projects team to support a growing portfolio of pharmaceutical and biotechnology projects across the United States. SimoTech is seeking an Automation Engineer to join our team. The ideal candidate will have at least 5 years’ experience using Emerson DeltaV within the pharmaceutical industry, along with batch automation experience<\/span>
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Key Responsibilities <\/span> <\/span> <\/span> <\/b>
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  •  <\/span><\/span><\/span>Oversight of System Integrator’s (SI) DeltaV Application Software Development.<\/span>
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  • Work in conjunction with the SI’s Engineers and Developers.<\/span>
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  • System integration of DeltaV with MES.<\/span>
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  • Review and approve documentation for the SI.<\/span>
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  • Take part in design and DeltaV application software reviews.<\/span>
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  • Agree on work practices related to source code reviews, configuration management, and testing with the SI.<\/span>
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  • Be a leader and mentor to up to 6 client -side Automation Area Leads across various areas of the site.<\/span>
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  • Ensure all work is completed in line with industry regulations and standards, including GAMP and 21CFR Part 11<\/span>

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    Requirements<\/h3>

    Key Requirements<\/span><\/span><\/span><\/b><\/span><\/span><\/span><\/span><\/b>
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    • Bachelor’s Degree in Engineering, Information Systems, Computer Sciences, Life Sciences or equivalent.<\/span>
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    • Ideally have 10 years+ experience using DeltaV in a pharmaceutical manufacturing, biopharma engineering or operations environment.<\/span>
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    • Be a Subject Matter Expert in DeltaV control system design.<\/span>
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    • Previous experience with Process Engineering is desirable.<\/span>
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    • Knowledge of GMP principles, industry regulatory requirements and computer system validation practices.<\/span>
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    • Excellent Communication and stakeholder management skills<\/span>
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    • Ability to work independently while contributing effectively within a team environment<\/span>
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    • Eligibility to work in the United States.<\/span>
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      Benefits<\/h3>
      What SimoTech Can Offer<\/span> <\/span> <\/span> <\/b> <\/span>
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      • Opportunity to work with large corporate clients on exciting capital projects.<\/span>
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      • Role provides a high degree of autonomy to allow the successful candidate to reach their full potential.<\/span>
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      • Develop new skills and enhance technical ability by working with innovative technologies in <\/span>
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      •   <\/span><\/span><\/span>We offer a hybrid working model for this role, balancing flexibility with business needs, <\/span>
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About the Company

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SimoTech