Automation Controls Engineer

Posted 5 Days Ago
Be an Early Applicant
Frederick, CO, USA
In-Office
103K-161K Annually
Mid level
Biotech
The Role
Responsible for GMP automation and controls for biopharma manufacturing: design, troubleshoot, and optimize PLC/DCS/SCADA/BAS systems; lead control system specs, change controls, and Part 11 compliance; support validation (FAT/SAT/IQ/OQ); and collaborate with QA, validation, process, and manufacturing teams to ensure uptime and regulatory compliance.
Summary Generated by Built In
Job Description

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. 

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 Details

    This 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

    Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

    Skills Required

    • Bachelor's or Master's Degree in Chemical, Mechanical, or Electrical Engineering or equivalent
    • 4+ years combined experience with automation/controls in pharma/biopharma and fine chemicals industry
    • Experience with Rockwell Automation Studio 5000
    • Experience with DeltaV
    • Experience with GE iFIX SCADA
    • Experience with FactoryTalk View
    • Experience with Allen-Bradley CompactLogix and ControlLogix PLCs
    • Experience with PanelViews and Allen-Bradley Variable Frequency Drives
    • Practical knowledge of GMP and GAMP5 and generation of controlled documents
    • Support control and computer system validation activities including FAT, SAT, IQ, OQ
    • On-the-floor automation/controls troubleshooting to ensure equipment uptime
    • Familiarity with bioprocessing unit operations and equipment
    • Knowledge of OT design principles, network architecture, virtual machines, and Thin Client architecture (ThinManager)
    • 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, and TCP/IP communication protocols
    • Experience applying ISA S88 and ISA S95 standards
    • Experience integrating OT and IT infrastructure and implementing appropriate cybersecurity posture
    • Ability to work independently and collaborate with Process Engineering, Manufacturing, Maintenance, Validation, and Quality

    Agilent Technologies Compensation & Benefits Highlights

    The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Agilent Technologies and has not been reviewed or approved by Agilent Technologies.

    • Retirement Support The core U.S. package highlights a generous 401(k) match as a strength. Retirement programs are positioned as competitive within the company’s total rewards.
    • Equity Value & Accessibility An Employee Stock Purchase Plan at a discount provides accessible equity and augments total compensation. Ownership opportunities are presented as a notable advantage alongside retirement benefits.
    • Leave & Time Off Breadth Flexible Time Off, company holidays, a personal holiday, and paid volunteer time create a broad leave offering. Time off can accrue into multiple weeks in the first year, supporting flexibility.

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    The Company
    HQ: Santa Clara, CA
    17,369 Employees
    Year Founded: 1999

    What We Do

    Analytical scientists and clinical researchers worldwide rely on Agilent to help fulfill their most complex laboratory demands. Our instruments, software, services and consumables address the full range of scientific and laboratory management needs—so our customers can do what they do best: improve the world around us. Whether a laboratory is engaged in environmental testing, academic research, medical diagnostics, pharmaceuticals, petrochemicals or food testing, Agilent provides laboratory solutions to meet their full spectrum of needs. We work closely with customers to help address global trends that impact human health and the environment, and to anticipate future scientific needs. Our solutions improve the efficiency of the entire laboratory, from sample prep to data interpretation and management. Customers trust Agilent for solutions that enable insights...for a better world.

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