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Senior Utilities Engineer (cGMP – Pharmaceutical) JD816690

JD816690

DPS Engineering is looking for a Senior Utilities Engineer to work with a BioPharma client in the Providence, RI area. Ideal candidates should have strong experience with clean and plant utility systems including but not limited to WFI, Clean Steam, HVAC, and other related utility systems.

Category:
Engineer Mechanical / Biomedical
Location:
Rhode Island
Years of Experience Req.:
8+
Date Posted:
08/07/2019
Days Remaining:
11
Employment Type:
Full-time
Education Level Req.:
Bachelors

Senior Utilities Engineer (cGMP – Pharmaceutical)               JD816690

Providence, RI

 

Summary:

                        

DPS is looking for a Senior Utilities Engineer to work with a BioPharma client in the Providence, RI area. Ideal candidates should have strong experience with clean and plant utility systems including but not limited to WFI, Clean Steam, HVAC, and other related utility systems.


Responsibilities:

  • Assist/Lead URS development for “Clean” and “Dirty” Utilities.
  • Assist with development of system boundaries and criticality assessments.
  • Review system specifications and component data sheets.
  • Manage P&IDs and incorporate redlines when/if design changes are required.
  • Attend equipment FATs and author or contribute to development of test documents.
  • Assist manufacturing with system shakedown, start-up and troubleshooting.
  • Review Submittals/Design Packages and ETOPs for accuracy and completeness.
  • Facilitate/participate in formal design reviews and design qualifications.
  • Assist automation and manufacturing with development of sequence of operations and phase flow paths for FRS/DDS development.
  • Assist in development of spare parts lists for input to CMMS.
  • Design and perform Engineering studies, as required.

 

Skills & Education                                                           

  • Bachelor’s degree in Mechanical Engineering or a related discipline.
  • Special knowledge requirements include biopharmaceutical and pharmaceutical process and facility design approaches, plus a solid understanding of cGMP requirements.
  • Must have superior understanding of MEP and clean utility systems.
  • Must have experience with leading mid-to-large capital projects for the pharmaceutical industry.
  • Must have experience with leading Utility Design requirements for mid-to-large capital projects for the pharmaceutical industry.
  • Experience working to regulatory standards: FDA, Good Engineering Practice (GEP), Good Manufacturing Procedures (GMP) and Good Documentation Procedures (GDP).
  • Ability to compile and analyz825268.039042e data.
  • Strong organiz825268.039042ational skills, oral and written communication and team attitude.
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