Process Engineer

Hyde Engineering ConsultantsRaleigh, NC
37dOnsite

About The Position

The Process Engineer provides site-based support to pharmaceutical and biopharmaceutical clients in the RTP Area. This role supports the conceptual design, basis of design, and detailed design of a production facility, providing support for FAT's off-site activities, SAT's, commissioning, automation, and/or Project Management. Are you looking for a meaningful career that makes a difference in the world? Hyde E+C contributes to helping people live longer, healthier lives by ensuring pharmaceutical and biopharmaceutical manufacturers can effectively and safely produce their life-enhancing and often life-saving medicines. To read more about Hyde's culture and benefits, visit our website: www.hyde-ec.com Hyde Engineering + Consulting is an equal opportunity, affirmative action employer. #LI-JS1 #LI-Hybrid Associate

Requirements

  • BS degree or higher in chemical or mechanical engineering
  • 10+ experience in the Biopharmaceutical industry
  • Engineering Drawings
  • Process Flow Diagrams (PFD)
  • Piping & Instrumentation Diagrams (P&ID)
  • General Arrangements (GA)
  • Floor Plans
  • Piping Plans
  • Vendor Mechanical Shop Drawings
  • Equipment Data Sheets, Valve & Instrument Lists Engineering Calculations
  • Equipment Sizing - tanks, pumps, filters, etc. Piping and valve sizing for pressure drop Utility consumptions Specifications
  • User Requirement Specs (URS) Functional Requirement Specs (FRS) Software Design Specs (SDS) Factory and Site Acceptance Testing ( FAT / SAT) Ability to read automation documentation and translating process information to automation berbiage Clean Utilities and/or Stainless Steel Process Equipment Design.
  • Large Powder Charging and Mixing Operations for Buffers (large SS tanks, mixers, material lifts, etc.) Familiar with ASME BPE standards Startup/Commissioning Activities
  • Spray Coverage Testing Cleaning Cycle Development/Optimization/Troubleshooting

Responsibilities

  • Support / lead the design and specification of cGMP equipment, processes and utilities.
  • Create and review project documentation
  • Concept Design (Redlines for Circuits and Flowpaths)
  • Engineering CIP Skid Capacity Assessment, Preliminary Hydraulics, New Equipment Sizing, New Line Sizing, New Valve, Instrument List.,)
  • Liaise with client end user groups to ensure correct specification of equipment and utilities.
  • Create Technical & Functional Specification for automated and manual equipment.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Industry

Professional, Scientific, and Technical Services

Number of Employees

101-250 employees

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