{"schemaVersion":"jobsearcher.job.v1","id":"b48789b0c8aa170a679dccd6","url":"https://jobsearcher.com/jobs/b48789b0c8aa170a679dccd6","canonicalUrl":"https://jobsearcher.com/jobs/b48789b0c8aa170a679dccd6","title":"Project Engineer","description":"Job Description The Project Engineer is an engineering professional who, working with little or no supervision, applies project management knowledge, engineering knowledge and ingenuity to complete medium sized projects from concept thru project closure, across disciplines and locations. Responsible for financial management, contractor management, and project oversight for equipment and facility projects. To be successful, the position will interface with Operations, Maintenance, Engineering, suppliers, and 3rd party contractor firms. Candidates should feel comfortable working in a plant environment. Strong communication and leadership skills along with technical knowledge of pharmaceutical/medical device projects are required.\nResponsibilities Responsible for supporting capital projects in the manufacturing plant, including front end planning activities.\nCoordinate multiple parties to complete project scopes on schedule, stay within budget and meet the expected quality.\nAssist with design of new equipment systems from preliminary design, specifications, budgeting, scheduling, and construction management.\nDevelop project schedules including setting targets for milestone activities and adhering to deadlines.\nTrack progress to ensure the project scope, cost, and schedule are being met. Manage the life‑cycle documentation of the equipment including generation and approval of user requirements, equipment and instrument specifications, equipment test plans, and system operating procedures.\nDevelop documents for FAT, SAT, and qualification activities for equipment.\nParticipate in FAT, SAT, startup, commissioning and qualification of equipment.\nWrite scope of work documents, award contracts, obtain estimates, select suppliers, and purchase equipment and services.\nReview drawings, supervise contractors, and participate in final project acceptance upon completion of construction.\nMaking effective decisions when presented with multiple options for how to progress with the project.\nCommunicating with management to keep the project aligned with their goals.\nPerforming quality control on the project throughout development to maintain the standards expected.\nRequirements Bachelor's Degree in Engineering, Science, or closely related discipline, or equivalent technical experience plus demonstrated competence.\nTechnical background in Pharmaceutical or similar GMP-regulated industry.\nExpertise in equipment design, design specifications, and PFD/P&ID development.\nExperience with manufacturing equipment commissioning and qualification.\nFamiliarity with PLC control systems.\nInteracts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.\nListens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations.\nWorks well with other engineers in a collaborative, fast‑paced goal‑driven environment.\nPossesses interpersonal skills to negotiate and reconcile differences.\nUnderstanding and management of procurement & contracting processes.\nExperience with automation and controls engineering.\nExperience with drug product and oral solid dosage manufacturing and equipment.\nCore Responsibilities Verification & Qualification documentation.\nFactory Acceptance Tests (FAT).\nSoftware Acceptance Tests.\nSite Acceptance Tests (SAT).\nSupport Equipment upgrades.\nAutomation‑related changes.\nPerform On‑site equipment testing.\nValidation execution.\nWork on Automation & control system‑heavy upgrades.\nMost Important CQV / Validation experience.\nAutomation & HMI exposure.\nStrong communication skills.\nImportant 4+ years experience.\nBachelor's degree (mandatory).\nOSD / Pharma equipment experience.\nCapital project exposure.\nTop 3–5 Skills / Experience Chemical or Mechanical Engineering degree strongly preferred.\nDevelop documents for FAT, SAT, and qualification activities for equipment.\nParticipate in FAT, SAT, startup, commissioning and qualification of equipment.\nExperience with automation and controls engineering preferred.\nExperience with drug product and oral solid dosage manufacturing and equipment preferred.\n\n#J-18808-Ljbffr","company":"Creative Solutions Services","rawCompany":"creative solutions services","city":"Bridgeport","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-07-03T03:21:02.662Z","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":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Project Engineer","description":"Job Description The Project Engineer is an engineering professional who, working with little or no supervision, applies project management knowledge, engineering knowledge and ingenuity to complete medium sized projects from concept thru project closure, across disciplines and locations. Responsible for financial management, contractor management, and project oversight for equipment and facility projects. To be successful, the position will interface with Operations, Maintenance, Engineering, suppliers, and 3rd party contractor firms. Candidates should feel comfortable working in a plant environment. Strong communication and leadership skills along with technical knowledge of pharmaceutical/medical device projects are required.\nResponsibilities Responsible for supporting capital projects in the manufacturing plant, including front end planning activities.\nCoordinate multiple parties to complete project scopes on schedule, stay within budget and meet the expected quality.\nAssist with design of new equipment systems from preliminary design, specifications, budgeting, scheduling, and construction management.\nDevelop project schedules including setting targets for milestone activities and adhering to deadlines.\nTrack progress to ensure the project scope, cost, and schedule are being met. Manage the life‑cycle documentation of the equipment including generation and approval of user requirements, equipment and instrument specifications, equipment test plans, and system operating procedures.\nDevelop documents for FAT, SAT, and qualification activities for equipment.\nParticipate in FAT, SAT, startup, commissioning and qualification of equipment.\nWrite scope of work documents, award contracts, obtain estimates, select suppliers, and purchase equipment and services.\nReview drawings, supervise contractors, and participate in final project acceptance upon completion of construction.\nMaking effective decisions when presented with multiple options for how to progress with the project.\nCommunicating with management to keep the project aligned with their goals.\nPerforming quality control on the project throughout development to maintain the standards expected.\nRequirements Bachelor's Degree in Engineering, Science, or closely related discipline, or equivalent technical experience plus demonstrated competence.\nTechnical background in Pharmaceutical or similar GMP-regulated industry.\nExpertise in equipment design, design specifications, and PFD/P&ID development.\nExperience with manufacturing equipment commissioning and qualification.\nFamiliarity with PLC control systems.\nInteracts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.\nListens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations.\nWorks well with other engineers in a collaborative, fast‑paced goal‑driven environment.\nPossesses interpersonal skills to negotiate and reconcile differences.\nUnderstanding and management of procurement & contracting processes.\nExperience with automation and controls engineering.\nExperience with drug product and oral solid dosage manufacturing and equipment.\nCore Responsibilities Verification & Qualification documentation.\nFactory Acceptance Tests (FAT).\nSoftware Acceptance Tests.\nSite Acceptance Tests (SAT).\nSupport Equipment upgrades.\nAutomation‑related changes.\nPerform On‑site equipment testing.\nValidation execution.\nWork on Automation & control system‑heavy upgrades.\nMost Important CQV / Validation experience.\nAutomation & HMI exposure.\nStrong communication skills.\nImportant 4+ years experience.\nBachelor's degree (mandatory).\nOSD / Pharma equipment experience.\nCapital project exposure.\nTop 3–5 Skills / Experience Chemical or Mechanical Engineering degree strongly preferred.\nDevelop documents for FAT, SAT, and qualification activities for equipment.\nParticipate in FAT, SAT, startup, commissioning and qualification of equipment.\nExperience with automation and controls engineering preferred.\nExperience with drug product and oral solid dosage manufacturing and equipment preferred.\n\n#J-18808-Ljbffr","datePosted":"2026-07-03T03:21:02.662Z","dateModified":"2026-07-03T03:21:02.662Z","hiringOrganization":{"@type":"Organization","name":"Creative Solutions Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bridgeport","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b48789b0c8aa170a679dccd6"},"url":"https://jobsearcher.com/jobs/b48789b0c8aa170a679dccd6"}}