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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