{"schemaVersion":"jobsearcher.job.v1","id":"c005d4e0351cad7feaec3d33","url":"https://jobsearcher.com/jobs/c005d4e0351cad7feaec3d33","canonicalUrl":"https://jobsearcher.com/jobs/c005d4e0351cad7feaec3d33","title":"MV06-022326 Process Project Manager","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\nValidation Process Project Manager\nResponsibilities:\nOwner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle).\nFocus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.\nManage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.\nChange Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity.\nDeliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.\nLead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.\nSafety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.\nInterface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.\nReviewing project plans and specifications.\nMonitoring contractor performance and ensuring adherence to contractual obligations.\nConducting regular site walkdowns to review quality and progress.\nEnsuring compliance with safety regulations and quality standards.\nDevelop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.\nWork closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.\nProvide engineering expertise and technical guidance throughout the project lifecycle.\nMaintain documentation of project activities, plans, designs, reports, and updates.\nMonitor project costs, manage budgets, and report on financial status.\nIdentify potential risks and develop mitigation strategies to ensure project success.\nEnsure all project activities meet or exceed industry standards, regulations, and company quality guidelines.\nRegularly update stakeholders on project progress, challenges, and changes in scope.\nAddress technical issues and project challenges, providing solutions to keep the project on track.\nQualifications:\nBachelor's Degree in Engineering or Science.\nMinimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.\nExperience in direct process / manufacturing areas.\nMust be fully bilingual (English / Spanish) with excellent oral skills.\nMust be proficient using MS Windows and Microsoft Office applications.\nStrong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.\nTechnical Writing skills and investigations processes.\nAvailable to work extended hours, possibility of weekends and holidays.","company":"Validation","rawCompany":"validation","city":"Washington","state":"DC","isRemote":false,"isActive":false,"createdAt":"2026-07-15T13:49:38.165Z","occupations":[{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"MV06-022326 Process Project Manager","description":"Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.\nWe are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:\nValidation Process Project Manager\nResponsibilities:\nOwner's Representative Duties: Act as the owner's representative, ensuring that the project aligns with the owner's vision and requirements. Lead and manage manufacturing capital project to safely achieve project objectives from conceptual design through operational verification (cradle to grave cycle).\nFocus on Electrical Infrastructure and Distribution Management: Supervise the construction of the building's electrical systems, ensuring compliance with all relevant codes and regulations.\nManage and oversee the construction of the pharmaceutical manufacturing facility, ensuring that all aspects of the project are completed on time, within budget, and to the highest quality standards.\nChange Order Management: Provide feedback and comments on change orders, ensuring that any modifications are necessary, cost-effective, and do not compromise the project's integrity.\nDeliver projects by managing project scope, schedule and budget while identifying and mitigating risks, all while prioritizing Safety First and Quality Always.\nLead with a disciplined, structured approach to project management based on compliance with Company Policies and Procedures.\nSafety/Environment: Develop and maintain safety and environmental execution plans for projects. Ensure compliance to safety and environmental policies, procedures, and work rules for project personnel, contractors, and subcontractors from conceptual design through operational verification. Be an active member of the site safety team.\nInterface/Communication: Develop and maintain effective communication with the project team, governance teams, business partners and other stakeholders, as the size of the project may dictate. Facilitate issue resolution, anticipate scope changes, and implement safely with quality, speed, and value.\nReviewing project plans and specifications.\nMonitoring contractor performance and ensuring adherence to contractual obligations.\nConducting regular site walkdowns to review quality and progress.\nEnsuring compliance with safety regulations and quality standards.\nDevelop detailed project plans, including scope, goals, deliverables, resource allocation, timelines, and budgets.\nWork closely with project managers, engineers, and stakeholders to ensure all aspects of the project are aligned and progressing smoothly.\nProvide engineering expertise and technical guidance throughout the project lifecycle.\nMaintain documentation of project activities, plans, designs, reports, and updates.\nMonitor project costs, manage budgets, and report on financial status.\nIdentify potential risks and develop mitigation strategies to ensure project success.\nEnsure all project activities meet or exceed industry standards, regulations, and company quality guidelines.\nRegularly update stakeholders on project progress, challenges, and changes in scope.\nAddress technical issues and project challenges, providing solutions to keep the project on track.\nQualifications:\nBachelor's Degree in Engineering or Science.\nMinimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.\nExperience in direct process / manufacturing areas.\nMust be fully bilingual (English / Spanish) with excellent oral skills.\nMust be proficient using MS Windows and Microsoft Office applications.\nStrong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.\nTechnical Writing skills and investigations processes.\nAvailable to work extended hours, possibility of weekends and holidays.","datePosted":"2026-07-15T13:49:38.165Z","dateModified":"2026-07-15T13:49:38.165Z","hiringOrganization":{"@type":"Organization","name":"Validation","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Washington","addressRegion":"DC","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c005d4e0351cad7feaec3d33"},"url":"https://jobsearcher.com/jobs/c005d4e0351cad7feaec3d33"}}