Automation Engineer
Thehive Careers · thehivecareers.com
West PointOn-siteSenior8–10 yrsContract
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The job in short
Automation and instrumentation engineering design and validation for biopharma manufacturing.
PLC
Details
- Found
- 22 d ago · posted 2026-10-03
- Location as listed
- West Point, PA, United States
- Role
- Engineer (other)
- Source
- The company’s own careers site
Full description
Job Details :
Industry:- Automation & Validation
Position:- Automation Engineer
Location: West Point-PA
Duration:- 1 year Contract
Description:
DAY-TO-DAY:
• Perform
automation and instrumentation and control engineering design services
for existing facility projects, including upgrades and capacity
expansions, equipment upgrading and replacement.
• Produce and review design drawings and specification documents (URS, FS, DS, etc.).
• Generate,
execute, and review design testing, generate and participate in
functional specification testing, and perform field inspection services.
• Generate, execute, and review Installation, Operational, and Performance Qualification protocols.
• Generate, review, and approve GMP Lifecycle Documents (e.g., risk documents, trace matrices, periodic review, etc.)
• Execute and track progress of change records.
MUST HAVES:
• 8-10 years' experience validation and programming experience with Werum MES software and DeltaV.
• Experience with Biopharmaceutical manufacturing, design or/and construction.
• Knowledge of process, utility and building control systems.
• Knowledge of GMP guidelines, experience in generation of controlled documents.
• Qualification experience related to control and computer systems.
• Ability to generate engineering drawings and specifications.
• Knowledge of ISA standards and practices for instrumentation.
• Knowledge of PID control theories and techniques.
• Knowledge of programmable logic controllers, and associated programming languages (RS Logix Preferred).
• Practical knowledge of distributed control systems, and associated programming languages ***Strong DeltaV Coding***
PLUSSES:
• Knowledge of computer aided manufacturing automation.
• Demonstrate good organizational and time utilization skills.
• Demonstrate good written and verbal communication skills.
• Ability
to comply with cGMP requirements (gowning, documentation, and
procedures) for performing work within the manufacturing facility.
• Demonstrate strong working knowledge of PC based programs and web-based systems.
• Ability to work most of the time independently with minimal direct supervision.
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