Job DescriptionJoin 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.
Key Responsibilities: - Subject matter expert for GMP manufacturing process control systems, Supervisory Control and Data Acquisition (SCADA) systems, Distributed Control Systems (DCS), 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.
Qualifications- 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, DeltaV, GE IFIX 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.
Preferred Skills: - 4+ 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.
- 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.
Additional DetailsThis job has a full time weekly schedule. Applications for this job will be accepted until at least June 24, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $103,200.00 - $161,250.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Travel Required: Occasional
Shift: Day
Duration: No End Date
Job Function: Manufacturing
