Automation Controls Engineer

Agilent Technologies • Frederick, CO

164d • $97,920 - $153,000

About The Position

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.

Requirements

• 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.

Nice To Haves

• 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.

Responsibilities

• 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.

Benefits

• Full-time equivalent pay range for this position is $97,920.00 - $153,000.00/yr plus eligibility for bonus, stock and benefits.

What This Job Offers

• Job Type: Full-time
• Industry: Computer and Electronic Product Manufacturing
• Education Level: Bachelor's degree