Bachelor's Degree in Mechanical, Electrical, Chemical (or BioChem), Manufacturing Engineering or equivalent education/experience
5 years of experience in pharma/biopharma and fine chemicals industry
4 years of experience with P&IDs, facility layouts, and standard operating procedures
4 years of experience in project lifecycle from design to qualification
4 years of Process Engineering experience
Responsibilities
Support design and qualification activities for capital projects from concept through validation
Oversee project management aspects including schedule, budget, and team coordination
Assist in technical transfer and scale-up of manufacturing processes
Support Environmental Health & Safety compliance and reviews
Conduct validation activities and review related protocols and reports
Engage in Quality Assurance processes including CAPA and audit responses
Perform job functions independently with minimal supervision
Benefits
Full-time weekly schedule
Eligibility for bonus and stock options
Comprehensive benefits package
Occasional travel opportunities
Day shift work hours
Full Job Description
Job Description
Responsibilities may include but are not limited to:
Support design, construction, commissioning and qualification activities for newly created capital projects from concept design through validation of new processes. Collaborate with Design Firm, Equipment Suppliers, Constructors and all other cross functional teams
Responsible for supporting a wide variety of capital projects throughout all phases of the project lifecycle, including the development of user requirement specifications, process design, equipment and instrumentation specification/selection, equipment procurement, installation, commissioning, qualification, and turn-over to manufacturing
Responsible for project management aspects including project schedule, budget, and coordination of multi-disciplinary teams
Support Chemical Development and Manufacturing Services groups with activities such as technical transfer and scale-up of processes into manufacturing
Support Environmental Health & Safety activities including Process Hazard Analysis, Pre-Startup Safety Review, and Process Safety Management compliance
Support Validation activities including review of Factory Acceptance Test and Site Acceptance Test (FAT/SAT) protocols and participating in FAT/SAT execution, review of installation, operational, and performance qualification (IQ/OQ/PQ) protocols, participating in IOPQ execution, and review of final reports
Support Quality Assurance activities including writing, review, and/or resolution of Change Controls (CC/CSC), Corrective and Preventive Actions (CAPAs), and audit responses
Perform job functions and responsibilities independently and with limited direction
Qualifications
Required
Bachelors Degree in Mechanical, Electrical, Chemical (or BioChem), Manufacturing Engineering or equivalent education/experience
5 years of experience in pharma/biopharma and fine chemicals industry
4 years of experience with P&IDs, facility layouts, mass and energy balances, solvent handling, equipment sizing calculations, user requirement specifications (URSs), standard operating procedures (SOPs) and process troubleshooting
4 years of experience participating in small to large-sized projects through all phases including design, design review, process hazard analysis, equipment procurement, installation, commissioning, and qualification is desirable
4 years of Process Engineering experience
Desired
Familiarity with current ASME BPE sanitary piping and equipment design standards, electrical standards such as National Fire Protection Association / National Electrical Code (NFPA 70 / NEC) and International Fire and Building Codes
Experience with design and programming of industrial control systems including SCADA, PLCs, and BAS and validation documentation including installation, operational and performance qualification (IQ/OQ/PQ) protocols
Ability to use AutoCAD, Revit, Visio
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least June 25, 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
About Agilent Technologies
Agilent Technologies is a global leader in life sciences, diagnostics, and applied chemical markets. With more than 50 years of insight and innovation, Agilent instruments, software, services, solutions, and people provide trusted answers to customers' most challenging questions. The company generated revenue of $5.34 billion in fiscal 2020 and employs 16,600 people worldwide.
