{"schemaVersion":"jobsearcher.job.v1","id":"b8faf9fa4189fa348f743e2a","url":"https://jobsearcher.com/jobs/b8faf9fa4189fa348f743e2a","canonicalUrl":"https://jobsearcher.com/jobs/b8faf9fa4189fa348f743e2a","title":"Sr. Project Manager","description":"Job Title: Sr. Project Manager\nDepartment: Project Management\nLocation: 4 Sunshine Blvd, Ormond Beach, FL 32174\nWork Schedule: Full time, in a production environment\n\nPosition Summary: Germfree is seeking a technically grounded Project Manager with a strong engineering foundation and demonstrated experience in regulated life sciences environments (GMP, FDA, ISO). This role will lead complex, multi-disciplinary projects involving the design, fabrication, and deployment of controlled environment solutions (e.g., cleanrooms, mobile labs, biocontainment equipment). The ideal candidate operates at the intersection of engineering rigor, regulatory compliance, and execution discipline, capable of driving projects from concept through validation and delivery while ensuring adherence to quality, cost, and schedule commitments.\n\nCore Responsibilities\nProject Leadership & Execution\nLead end-to-end project execution (initiation through commissioning and closeout)\nDevelop and manage integrated project plans, schedules, budgets, and resource allocations\nDrive cross-functional coordination across engineering, manufacturing, quality, supply chain, and field teams\nLead and support equipment-focused projects, including isolators, containment systems, and other critical GMP processing equipment, from design through FAT/SAT and final commissioning\nCoordinate closely with engineering, vendors, and quality to ensure equipment meets URS requirements, integrates seamlessly into broader systems, and complies with GMP, validation, and documentation standards\nMaintain accountability for on-time, on-budget, and in-spec project delivery\nWork inside PMO and help develop consistency in standardization, tools, and methods\nOpen to travel including domestic and international\nTechnical & Engineering Integration\nInterface directly with engineering teams (mechanical, electrical, process, controls) internally and client facing to ensure design intent aligns with project requirements\nTranslate customer/user requirements into executable project scope and technical deliverables\nIdentify and manage technical risks, trade-offs, and change controls\nGMP & Regulatory Compliance\nEnsure all project activities align with GMP, FDA, and applicable regulatory standards\nSupport validation efforts (IQ/OQ/PQ), documentation, and quality system compliance\nCoordinate with Quality Assurance to ensure proper documentation, traceability, and audit readiness\nCustomer & Stakeholder Management\nServe as primary point of contact for customers throughout project lifecycle\nLead project reviews, status updates, and milestone presentations\nManage expectations and proactively resolve issues\nFinancial & Commercial Oversight\nTrack project costs, margins, and financial performance\nSupport change order management and scope adjustments\nPartner with sales and leadership on contract execution and risk mitigation\n\nRequired Qualifications\nEducation & Experience\nBachelor’s degree in Engineering (Mechanical, Electrical, Chemical, or related)\n5–10+ years of project management experience in life sciences, biotech, pharma, or regulated environments\nConstruction experience in a CGMP cleanroom environment is a plus.\nDemonstrated experience managing capital projects within GMP-regulated environments, biopharma or GC experience is a plus.\nTechnical & Domain Expertise\nStrong understanding of cleanroom systems, controlled environments, or similar engineered systems (HVAC, process systems, modular builds)\nWorking knowledge of GMP, FDA regulations, and qualification processes (IQ/OQ/PQ)\nExperience with engineering documentation, design reviews, and change control processes\nProject Management Capability\nProven track record managing complex, multi-disciplinary projects\nStrong command of project management tools (Primavera, P6, MSP, etc)\nFamiliarity with formal PM methodologies (PMP preferred but not required)\nPreferred Qualifications\nExperience with modular construction, mobile labs, or prefabricated systems\nExposure to biosafety levels (BSL), containment systems, or advanced lab environments\nExperience with GMP-critical equipment systems such as isolators, containment systems, and aseptic processing equipment, including integration into facility and process environments\nPMP certification or equivalent\nExperience working with government contracts (DoD, BARDA, NIH) is a plus\nKey Competencies\nExecution Discipline: Drives projects with urgency and accountability\nTechnical Credibility: Earns trust with engineering and technical stakeholders\nRegulatory Mindset: Understands and respects GMP rigor and documentation standards\nProblem Solving: Navigates ambiguity and resolves complex issues efficiently\nCommunication: Clear, structured communicator with both technical and non-technical audiences\nOwnership Mentality: Acts like a business owner over project outcomes\n\nWhy You’ll Love Germfree: We want to make sure that you can expect excellence from us as well, and so we provide the best work environment possible to allow you to love what you do. As stated before, we will give you everything you need to succeed and will also motivate you to push yourself in new and positive ways. Whether this is meeting new people, working on projects you are passionate about, or innovating a process – we will help make it happen. A super hardcore work ethic, talent for building things, common sense & trustworthiness are required. At Germfree, you will get out exactly what you put in, and we know you can excel with us.\n\nWe are proud to be an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. We value and celebrate the unique backgrounds, perspectives, and experiences of all individuals, and we believe that diversity drives innovation and growth. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status.\nWe also maintain a drug-free workplace. Offers of employment may be contingent upon the successful completion of a drug screening, in accordance with applicable laws and company policies.","company":"Germfree Laboratories","rawCompany":"germfree laboratories","city":"Ormond Beach","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-08-06T13:59:32.582Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"11-9021.00","title":"Construction Managers","slug":"construction-managers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"236220","title":"Commercial and Institutional Building Construction","slug":"commercial-and-institutional-building-construction"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sr. Project Manager","description":"Job Title: Sr. Project Manager\nDepartment: Project Management\nLocation: 4 Sunshine Blvd, Ormond Beach, FL 32174\nWork Schedule: Full time, in a production environment\n\nPosition Summary: Germfree is seeking a technically grounded Project Manager with a strong engineering foundation and demonstrated experience in regulated life sciences environments (GMP, FDA, ISO). This role will lead complex, multi-disciplinary projects involving the design, fabrication, and deployment of controlled environment solutions (e.g., cleanrooms, mobile labs, biocontainment equipment). The ideal candidate operates at the intersection of engineering rigor, regulatory compliance, and execution discipline, capable of driving projects from concept through validation and delivery while ensuring adherence to quality, cost, and schedule commitments.\n\nCore Responsibilities\nProject Leadership & Execution\nLead end-to-end project execution (initiation through commissioning and closeout)\nDevelop and manage integrated project plans, schedules, budgets, and resource allocations\nDrive cross-functional coordination across engineering, manufacturing, quality, supply chain, and field teams\nLead and support equipment-focused projects, including isolators, containment systems, and other critical GMP processing equipment, from design through FAT/SAT and final commissioning\nCoordinate closely with engineering, vendors, and quality to ensure equipment meets URS requirements, integrates seamlessly into broader systems, and complies with GMP, validation, and documentation standards\nMaintain accountability for on-time, on-budget, and in-spec project delivery\nWork inside PMO and help develop consistency in standardization, tools, and methods\nOpen to travel including domestic and international\nTechnical & Engineering Integration\nInterface directly with engineering teams (mechanical, electrical, process, controls) internally and client facing to ensure design intent aligns with project requirements\nTranslate customer/user requirements into executable project scope and technical deliverables\nIdentify and manage technical risks, trade-offs, and change controls\nGMP & Regulatory Compliance\nEnsure all project activities align with GMP, FDA, and applicable regulatory standards\nSupport validation efforts (IQ/OQ/PQ), documentation, and quality system compliance\nCoordinate with Quality Assurance to ensure proper documentation, traceability, and audit readiness\nCustomer & Stakeholder Management\nServe as primary point of contact for customers throughout project lifecycle\nLead project reviews, status updates, and milestone presentations\nManage expectations and proactively resolve issues\nFinancial & Commercial Oversight\nTrack project costs, margins, and financial performance\nSupport change order management and scope adjustments\nPartner with sales and leadership on contract execution and risk mitigation\n\nRequired Qualifications\nEducation & Experience\nBachelor’s degree in Engineering (Mechanical, Electrical, Chemical, or related)\n5–10+ years of project management experience in life sciences, biotech, pharma, or regulated environments\nConstruction experience in a CGMP cleanroom environment is a plus.\nDemonstrated experience managing capital projects within GMP-regulated environments, biopharma or GC experience is a plus.\nTechnical & Domain Expertise\nStrong understanding of cleanroom systems, controlled environments, or similar engineered systems (HVAC, process systems, modular builds)\nWorking knowledge of GMP, FDA regulations, and qualification processes (IQ/OQ/PQ)\nExperience with engineering documentation, design reviews, and change control processes\nProject Management Capability\nProven track record managing complex, multi-disciplinary projects\nStrong command of project management tools (Primavera, P6, MSP, etc)\nFamiliarity with formal PM methodologies (PMP preferred but not required)\nPreferred Qualifications\nExperience with modular construction, mobile labs, or prefabricated systems\nExposure to biosafety levels (BSL), containment systems, or advanced lab environments\nExperience with GMP-critical equipment systems such as isolators, containment systems, and aseptic processing equipment, including integration into facility and process environments\nPMP certification or equivalent\nExperience working with government contracts (DoD, BARDA, NIH) is a plus\nKey Competencies\nExecution Discipline: Drives projects with urgency and accountability\nTechnical Credibility: Earns trust with engineering and technical stakeholders\nRegulatory Mindset: Understands and respects GMP rigor and documentation standards\nProblem Solving: Navigates ambiguity and resolves complex issues efficiently\nCommunication: Clear, structured communicator with both technical and non-technical audiences\nOwnership Mentality: Acts like a business owner over project outcomes\n\nWhy You’ll Love Germfree: We want to make sure that you can expect excellence from us as well, and so we provide the best work environment possible to allow you to love what you do. As stated before, we will give you everything you need to succeed and will also motivate you to push yourself in new and positive ways. Whether this is meeting new people, working on projects you are passionate about, or innovating a process – we will help make it happen. A super hardcore work ethic, talent for building things, common sense & trustworthiness are required. At Germfree, you will get out exactly what you put in, and we know you can excel with us.\n\nWe are proud to be an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. We value and celebrate the unique backgrounds, perspectives, and experiences of all individuals, and we believe that diversity drives innovation and growth. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status.\nWe also maintain a drug-free workplace. Offers of employment may be contingent upon the successful completion of a drug screening, in accordance with applicable laws and company policies.","datePosted":"2026-08-06T13:59:32.582Z","dateModified":"2026-08-06T13:59:32.582Z","hiringOrganization":{"@type":"Organization","name":"Germfree Laboratories","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Ormond Beach","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b8faf9fa4189fa348f743e2a"},"url":"https://jobsearcher.com/jobs/b8faf9fa4189fa348f743e2a"}}