{"schemaVersion":"jobsearcher.job.v1","id":"1f670ff94156d2f9742ff8f2","url":"https://jobsearcher.com/jobs/1f670ff94156d2f9742ff8f2","canonicalUrl":"https://jobsearcher.com/jobs/1f670ff94156d2f9742ff8f2","title":"Project Engineer","description":"Description\r\nThe Project Engineer is responsible for providing engineering and technical leadership for equipment and infrastructure projects within a pharmaceutical manufacturing environment. This role supports the planning, design, execution, and closeout of engineering projects related to process equipment, utilities, facilities, and manufacturing systems.\r\nThe Project Engineer works cross-functionally with MS&T, Operations, Quality, Validation, Maintenance, EHS, and Supply Chain to ensure projects are technically sound, compliant with cGMP requirements, delivered safely, and completed on schedule and within budget.\r\nRequirements\r\nEngineering & Technical Execution\r\nDevelop technical project scopes, equipment specifications, and engineering documentation.\r\nPrepare and review User Requirement Specifications (URS), functional/design specifications, and bid packages.\r\nReview P&IDs, equipment layouts, and vendor submittals to ensure alignment with process and site standards.\r\nReview and provide feedback on vendor RFIs; coordinate responses with cross-functional team members to ensure alignment.\r\nProvide engineering oversight during equipment fabrication, installation, commissioning, and startup.\r\nSupport FAT/SAT, commissioning activities, and validation efforts (IQ/OQ/PQ).\r\nEnsure compliance with cGMP, quality standards, and environmental health & safety (EHS) requirements.\r\nProject Coordination\r\nSupport development and maintenance of project schedules, budgets, and resource plans.\r\nCoordinate cross-functional activities to ensure timely completion of deliverables.\r\nTrack project progress and communicate updates to stakeholders and leadership.\r\nAssist in risk identification, impact assessment, and development of mitigation strategies.\r\nSupport change control processes and ensure proper documentation throughout the project lifecycle.\r\nVendor & Contractor Support\r\nAssist in development of RFPs and technical bid evaluations.\r\nReview vendor deliverables to confirm compliance with project requirements.\r\nAssist with coordination of vendor activities during equipment installation and startup.\r\nReview invoices against scope completion and project milestones.\r\nDocumentation & Continuous Improvement\r\nMaintain accurate and complete engineering documentation.\r\nSupport continuous improvement initiatives within engineering, project management, and manufacturing operations.\r\nParticipate in audit readiness activities and regulatory inspections as needed.\r\nOther duties as assigned.\r\nRequired Experience\r\n5-7 years of engineering experience within pharmaceutical, biotech, or other regulated manufacturing environments.\r\nExperience supporting capital projects and equipment installations.\r\nWorking knowledge of pharmaceutical manufacturing processes and GMP requirements.\r\nUnderstanding of engineering documentation including URS, construction documents, P&IDs, process flow diagrams, and equipment and systems specifications.\r\nFamiliarity with validation lifecycle concepts (IQ/OQ/PQ/PV).\r\nTechnical Skills\r\nProficiency in MS Office (MS Project, Excel, Word, and PowerPoint), Smartsheet, Autodesk 2D and 3D Software.\r\nExperience with document management systems such as SharePoint, OneDrive, or similar platforms.\r\nExperience with contractor document management systems such as Procore or BIM 360.\r\nAbility to interpret construction and engineering drawings, and technical documents.\r\nEducation & Certifications\r\nBachelor's degree in Engineering (Mechanical, Chemical, Electrical, Industrial, or related discipline).\r\nPE license or EIT certification preferred.\r\nPMP certification a plus but not required.\r\nKey Attributes\r\nExcellent written and oral communication skills\r\nStrong organizational skills\r\nStrong attention to detail\r\nExhibits the highest level of reasoned judgment, discretion, and integrity. Integrity is our defining characteristic at Phlow\r\nCollaborates with others to achieve shared objectives. At Phlow, we are focused on working together, accepting feedback, and making it about results\r\nAbility to thrive in a fast-moving, continuous learning environment; iterating and learning as a team\r\nActive listener with a curious and open mind\r\nSteadfastly pursues excellence in execution\r\nExhibits high regard for quality assurance and safety\r\nServant leader\r\nPhysical Requirements\r\nConstantly required to see to utilize computer screens and monitors to perform job duties including reading & writing, as well as when presenting information and communicating with others.\r\nFrequently required to talk or hear to communicate with employees, candidates, vendors, and others, including presenting information in front of groups.\r\nFrequently required to reach with arms and hands performing repetitive motions and using finger dexterity to work primarily at a computer keyboard and with a mouse.\r\nFrequently required to sit, and occasionally required to stand or walk to move around primarily in an office environment.\r\nOccasionally lift and/or move up to 10 pounds.\r\nThis position may require up to 5% travel with occasional increase in travel demands based on business needs","company":"Phlow","rawCompany":"phlow","city":"Charlottesville","state":"VA","isRemote":false,"isActive":false,"createdAt":"2026-04-14T03:17:24.846Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"}],"industries":[{"code":"237990","title":"Other Heavy and Civil Engineering Construction","slug":"other-heavy-and-civil-engineering-construction"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Project Engineer","description":"Description\r\nThe Project Engineer is responsible for providing engineering and technical leadership for equipment and infrastructure projects within a pharmaceutical manufacturing environment. This role supports the planning, design, execution, and closeout of engineering projects related to process equipment, utilities, facilities, and manufacturing systems.\r\nThe Project Engineer works cross-functionally with MS&T, Operations, Quality, Validation, Maintenance, EHS, and Supply Chain to ensure projects are technically sound, compliant with cGMP requirements, delivered safely, and completed on schedule and within budget.\r\nRequirements\r\nEngineering & Technical Execution\r\nDevelop technical project scopes, equipment specifications, and engineering documentation.\r\nPrepare and review User Requirement Specifications (URS), functional/design specifications, and bid packages.\r\nReview P&IDs, equipment layouts, and vendor submittals to ensure alignment with process and site standards.\r\nReview and provide feedback on vendor RFIs; coordinate responses with cross-functional team members to ensure alignment.\r\nProvide engineering oversight during equipment fabrication, installation, commissioning, and startup.\r\nSupport FAT/SAT, commissioning activities, and validation efforts (IQ/OQ/PQ).\r\nEnsure compliance with cGMP, quality standards, and environmental health & safety (EHS) requirements.\r\nProject Coordination\r\nSupport development and maintenance of project schedules, budgets, and resource plans.\r\nCoordinate cross-functional activities to ensure timely completion of deliverables.\r\nTrack project progress and communicate updates to stakeholders and leadership.\r\nAssist in risk identification, impact assessment, and development of mitigation strategies.\r\nSupport change control processes and ensure proper documentation throughout the project lifecycle.\r\nVendor & Contractor Support\r\nAssist in development of RFPs and technical bid evaluations.\r\nReview vendor deliverables to confirm compliance with project requirements.\r\nAssist with coordination of vendor activities during equipment installation and startup.\r\nReview invoices against scope completion and project milestones.\r\nDocumentation & Continuous Improvement\r\nMaintain accurate and complete engineering documentation.\r\nSupport continuous improvement initiatives within engineering, project management, and manufacturing operations.\r\nParticipate in audit readiness activities and regulatory inspections as needed.\r\nOther duties as assigned.\r\nRequired Experience\r\n5-7 years of engineering experience within pharmaceutical, biotech, or other regulated manufacturing environments.\r\nExperience supporting capital projects and equipment installations.\r\nWorking knowledge of pharmaceutical manufacturing processes and GMP requirements.\r\nUnderstanding of engineering documentation including URS, construction documents, P&IDs, process flow diagrams, and equipment and systems specifications.\r\nFamiliarity with validation lifecycle concepts (IQ/OQ/PQ/PV).\r\nTechnical Skills\r\nProficiency in MS Office (MS Project, Excel, Word, and PowerPoint), Smartsheet, Autodesk 2D and 3D Software.\r\nExperience with document management systems such as SharePoint, OneDrive, or similar platforms.\r\nExperience with contractor document management systems such as Procore or BIM 360.\r\nAbility to interpret construction and engineering drawings, and technical documents.\r\nEducation & Certifications\r\nBachelor's degree in Engineering (Mechanical, Chemical, Electrical, Industrial, or related discipline).\r\nPE license or EIT certification preferred.\r\nPMP certification a plus but not required.\r\nKey Attributes\r\nExcellent written and oral communication skills\r\nStrong organizational skills\r\nStrong attention to detail\r\nExhibits the highest level of reasoned judgment, discretion, and integrity. Integrity is our defining characteristic at Phlow\r\nCollaborates with others to achieve shared objectives. At Phlow, we are focused on working together, accepting feedback, and making it about results\r\nAbility to thrive in a fast-moving, continuous learning environment; iterating and learning as a team\r\nActive listener with a curious and open mind\r\nSteadfastly pursues excellence in execution\r\nExhibits high regard for quality assurance and safety\r\nServant leader\r\nPhysical Requirements\r\nConstantly required to see to utilize computer screens and monitors to perform job duties including reading & writing, as well as when presenting information and communicating with others.\r\nFrequently required to talk or hear to communicate with employees, candidates, vendors, and others, including presenting information in front of groups.\r\nFrequently required to reach with arms and hands performing repetitive motions and using finger dexterity to work primarily at a computer keyboard and with a mouse.\r\nFrequently required to sit, and occasionally required to stand or walk to move around primarily in an office environment.\r\nOccasionally lift and/or move up to 10 pounds.\r\nThis position may require up to 5% travel with occasional increase in travel demands based on business needs","datePosted":"2026-04-14T03:17:24.846Z","dateModified":"2026-04-14T03:17:24.846Z","hiringOrganization":{"@type":"Organization","name":"Phlow","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Charlottesville","addressRegion":"VA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"1f670ff94156d2f9742ff8f2"},"url":"https://jobsearcher.com/jobs/1f670ff94156d2f9742ff8f2"}}