Automation Controls Engineer

Agilent Technologies-posted 3 months ago
$97,920 - $153,000/Yr
Full-time
Frederick, CO
Computer and Electronic Product Manufacturing
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Join a growing team with this exciting opportunity for an Automation Controls Engineer at our Frederick, Colorado GMP facility. Work in our dynamic, fast-paced, API-Biopharma manufacturing environment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) based therapeutics.

  • Subject matter expert for GMP manufacturing process control systems, Supervisory Control and Data Acquisition (SCADA) systems, distributed PLCs, Building Automation System (BAS), and automation/controls systems associated with various independent pharma/bioprocessing equipment.
  • Support on-the-floor automation/controls troubleshooting as needed to ensure equipment uptime and manufacturing operations.
  • Responsible for implementing system improvement, fixes, and process optimization PLC and SCADA code changes.
  • Lead plant control system detailed design specifications, relevant change controls, and 21 CFR Part 11 data integrity compliance.
  • Support control and computer system validation activities including review and execution of automation Factory Acceptance Tests, Site Acceptance Tests, and Installation and Operational Qualification protocols.
  • Collaborate with quality assurance to support change controls (CC/CSC), Corrective and Preventative Actions (CAPA), and audit responses.
  • Bachelor's or Master's Degree in Chemical, Mechanical, or Electrical Engineering or equivalent; may consider equivalent combination of training, education, and relevant experience.
  • 4+ years combined experience with automation/controls in pharma/biopharma and fine chemicals industry.
  • Experience with Rockwell Automation Studio 5000, Ignition SCADA, FactoryTalk View, Allen-Bradley CompactLogix, ControlLogix PLCs, PanelViews, Allen-Bradley Variable Frequency Drives, Thin client architecture, and ThinManager.
  • Practical knowledge of GMP, GAMP5, and experience in the generation of controlled documents.
  • Experience in applying ISA S88, S95, etc standards and implementation of the best practices.
  • Experience integrating OT and IT infrastructure for resiliency and appropriate cyber security posture.
  • Familiarity with computer hardware, virtualized systems, and network architecture.
  • 5+ years of experience working in a GMP / FDA regulated environment.
  • Familiarity with bioprocessing unit operations and associated equipment.
  • Knowledge of OT design principals, network architecture, virtual machines, and Thin Client architecture.
  • Ability to interpret and create electrical one-line diagrams and controls drawings.
  • Experience with Siemens Desigo CC based BAS software.
  • Experience with ASI, HART, Profibus, DHP, TCP/IP communication protocols.
  • Ability to work independently with limited direct supervision to complete assigned tasks and projects.
  • Ability to interact closely and maintain relationships with Process Engineering, Manufacturing Sciences, Manufacturing, Maintenance, Validation, and Quality organizations.
  • Full-time equivalent pay range for this position is $97,920.00 - $153,000.00/yr plus eligibility for bonus, stock and benefits.
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