CQV Engineer – Downstream

CQV Engineer - Downstream - Life Sciences - Contract - Massachusetts

Our client, a leading partner to pharmaceutical, biotech and nutrition markets, has an exciting opening for a CQV Engineer – Downstream for their new Capex investment project. 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 (or > 5yr equiv work experience)

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

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