Qualifications
Responsibilities
Benefits
Join a growing team with this exciting new opportunity for aPrincipalAutomationEngineerin ourAutomationgroupsupportingdesign, construction, and operationof pharmaceutical facilities. Work in our dynamic, fast paced, API-Biopharma manufacturingenvironment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) basedtherapeutics.
Responsibilities may include but are not limited to:
Function as Automation Project Lead for a large-scale greenfield manufacturingexpansion
Evaluate and recommendthe preferred automation integration platform for a new facility.
Establishautomationrequirementsfor site process control, independent bioprocessing skids,and building management systems.
Establish requirements for plant data historian system
Establish requirements for IT/OT infrastructure and system integration
Evaluate distributed control system (DCS) and plant control systems (PCS) to define best platform for new production facility based on site location and functionality
Develop Manufacturing Execution System (MES) platform and integration requirements.
CoordinateMES and process data collectionfor Electronic Batch Records (EBR)implementation.
Supportofindustrial control systems.
Manage contract resources forAutomationIntegration,plant data historian integration, andManufacturing Execution Systemsintegration
Support Commissioning, Qualification, Validation (CQV)activitiesand function as primary point of contact on automation projects for CQV
A successful person in this position will:
Utilize leadership skills to manage staff and contractors
Exposure toCSV/MES/DCS/PCS/SCADA/PLC/LIMS/EBR/QMS/PDH
Tools: Agile PLM, MS Project/Smartsheet,RAM CMMS, TMS DCS
Demonstrate the Agilent core values ofintegrity, trust, respect, teamwork, accountability, focus, innovation, andspeaking up.
Bachelors /Masterdegree or equivalent.
Postgraduate, certification, and/or license may berequired.
10+yearsrelevant experience forthis leadership position.
Demonstrated communication skills, including verbal and written communication, in contact withvendors, internal customers, and employees.
Knowledge of Good Manufacturing Practices (GMP), good automation manufacturing processes (GAMP),and Good Documentation Practices (GDP).
Knowledge of data integrity and 21CFR11 requirements and for the design qualification of Biotech/pharmaceutical GMP computerized systems
Knowledge of computerizedsystemsserver and personal computer hardware, networking, operating systems, integrated architecture, cybersecurityand resiliency.
Knowledge of automation standards includingISA-88 (S88), ISA/IEC62443,ISA-95, andISA-101
Knowledge of OSHA, local safety guidelines, lock-out tag-out, and hot work permits.
Desired:
Experience with supervision of personnel / coordination of group work activities.
Experience in a highly regulated industry with strict documentation requirements
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least July 13, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $146,640.00 - $229,125.00/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/locationsTravel Required:About Agilent Technologies
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