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CQV Engineer

  1. Brazil
San Juan
  1. Contract
Competitive
  1. Commissioning, Qualification and Validation
35497d

This vacancy has now expired

CQV Engineer - Pharmaceuticals - Puerto Rico - Contract Position 

Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer for their new Capex investment project in Puerto Rico. As a scientific and technology innovator, this is a superb opportunity to onboard as our client continues to make strides towards a healthier world for all.


CQV Engineer - Downstream Responsibilities:
  • Author/review/update URS and FS documentation (some automation experience preferred).
  • Highlight PID process flow path diagrams for Functional Specifications.
  • Review and provide feedback on PIDs.
  • Review and provide feedback on component lists and data sheets.  Author/review commissioning protocols (IQ/OQ) including CIP/SIP.
  • Perform P&ID walkdowns to record As-Built conditions and provide feedback to Engineering.
  • Assist with IQ and commissioning/start-up as necessary including protocol execution and troubleshooting.

About you:
  • Commissioning, PIDs, biotech, cGMP, ISA data sheets, valve sizing, pump sizing, single-use, CIP/SIP, URS, FS/FDS/FRS, communication, organization, problem solving, hands-on, self-motivated. UF, Chromatography, and/or Bioreactor experience preferred.
  • Automation experience DeltaV/PLC preferred.
  • BS Chem/Mech Engineering

Are you a good fit for a CQV Engineer? Get in touch with us today.


 
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