Quanta Consultancy Services Ltd
Overview
Project Engineer - US, Ohio - 12-24 Month Contract This is a fantastic opportunity for a Project Engineer to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn. Responsibilities
Technical Oversight & Review: Review vendor engineering packages, drawings, submittals, and ensure compliance with cGMP/owner standards; support and witness FATs/SATs. Project Management & CCC/Turnover: Track procurement through CQV readiness; manage turnover documentation; support partial turnover strategies. Coordination & Integration: Interface with vendors, EPCM/GC, commissioning teams; oversee utility tie-ins and integration. Provide scope updates, risk reports, CCC trackers, lessons learned. Qualifications
Requires extensive experience on large-scale pharmaceutical, biotech, or regulated process projects. Familiarity with large process vessels, bioreactors, modular/skid systems. Understanding of ASME pressure vessel code, sanitary design, automation integration, and cGMP compliance. Prior Owner’s Rep/EPCM/consulting role experience preferred. If this role is of interest, please apply now! #LI-AN1
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Project Engineer - US, Ohio - 12-24 Month Contract This is a fantastic opportunity for a Project Engineer to join our major, global pharmaceutical client on their latest new-build project based in Ohio, this is a large-scale greenfield capital project and investing more than $1bn. Responsibilities
Technical Oversight & Review: Review vendor engineering packages, drawings, submittals, and ensure compliance with cGMP/owner standards; support and witness FATs/SATs. Project Management & CCC/Turnover: Track procurement through CQV readiness; manage turnover documentation; support partial turnover strategies. Coordination & Integration: Interface with vendors, EPCM/GC, commissioning teams; oversee utility tie-ins and integration. Provide scope updates, risk reports, CCC trackers, lessons learned. Qualifications
Requires extensive experience on large-scale pharmaceutical, biotech, or regulated process projects. Familiarity with large process vessels, bioreactors, modular/skid systems. Understanding of ASME pressure vessel code, sanitary design, automation integration, and cGMP compliance. Prior Owner’s Rep/EPCM/consulting role experience preferred. If this role is of interest, please apply now! #LI-AN1
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