CQV Process Equipment Engineer
Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 11, 2026. QCS Staffing scores A on the Alion truth index.
Develop and own the Commissioning, Qualification & Validation (CQV) activities associated with your project, aligned to project schedule and GMP requirements up to Performance Qualification of all systems and equipment. Act as Client C&Q Lead for the project. Throughout execution; coordinate all commissioning and qualification activities and act as single point of contact for CQV interfaces.Plan and lead execution of system commissioning and qualification of equipment in accordance with project schedule and phased release of areas.Oversee and coordinate Commissioning Partner and commissioning sub-contractors; manage performance against scope and programme. Commissioning partner responsible for commissioning of utility and facility systems.Interface with internal stakeholders including Quality, Manufacturing, Operational Readiness, Engineering, EHS, QC.
Experience required:
Degree qualification in Engineering, Science, related discipline or relevant experienceRelevant experience in pharmaceutical and GMP regulated manufacturing environments.Extensive GMP experience, with demonstrable experience.Proven track record of commissioning and qualification involving solid dosage process equipment installation.Experience planning and delivering complex commissioning and qualification of systems.
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