{"schemaVersion":"jobsearcher.job.v1","id":"7fdb83c87dcf2bcaacbbb5ed","url":"https://jobsearcher.com/jobs/7fdb83c87dcf2bcaacbbb5ed","canonicalUrl":"https://jobsearcher.com/jobs/7fdb83c87dcf2bcaacbbb5ed","title":"MES Program manager","description":"We are seeking an experienced MES Program Manager to lead and coordinate large-scale Manufacturing Execution System (MES) initiatives within a regulated pharmaceutical environment. This role requires strong program leadership capabilities, cross-functional coordination, and oversight of multiple workstreams related to MES implementation, validation, and system integration. The ideal candidate brings extensive experience managing complex programs in pharmaceutical or biotech manufacturing environments and can effectively align technical, operational, and business stakeholders to ensure successful delivery.Location & Work ModeLocation: TorontoWork Mode: HybridSeniority: Senior (7–10 years of experience)Key ResponsibilitiesLead and oversee MES programs across multiple project phases, from planning and requirements gathering through deployment and hypercareCoordinate cross-functional teams including automation, IT, manufacturing operations, validation, engineering, and qualityManage dependencies and interfaces between MES and connected systems such as PLCs, SCADA, historians, and ERP platformsEnsure alignment between business objectives, technical execution, timelines, and program deliverablesOversee Computer System Validation (CSV) activities and ensure compliance with GMP and regulatory requirementsMonitor program scope, budget, risks, timelines, and resource allocation while providing regular status updates to leadershipDrive governance, stakeholder communication, and decision-making across multiple project streamsManage external vendors, consultants, and system integrators to ensure successful delivery of milestones and deliverablesSupport issue resolution, escalation management, and continuous improvement initiativesPromote best practices in program management, quality, compliance, and operational excellenceRequired ProfileMust-Have Qualifications7–10 years of experience managing MES programs or large-scale MES projects within the pharmaceutical or biotech industryProven experience delivering MES implementations in regulated manufacturing environmentsStrong understanding of manufacturing automation architecture, including PLCs, SCADA, MES, historians, and ERP integrationsExperience overseeing validation planning and CSV activitiesSolid knowledge of GMP regulations and compliance expectationsDemonstrated leadership experience managing multidisciplinary teams and complex stakeholder environmentsStrong program management, communication, organizational, and risk management skillsCompensationExpected Compensation Range: 100Hr-150Hr.The final compensation offered will be determined based on the candidate's level of experience, skills, and qualifications, in compliance with applicable pay transparency requirements.Canadian Experience Requirement: No Canadian work experience is required for this position. Candidates are encouraged to apply regardless of previous Canadian experience.Artificial Intelligence (AI) Disclosure: No Artificial Intelligence (AI) tools are used in the screening, assessment, or selection of candidates for this position. All stages of the recruitment process are conducted by human recruiters and hiring managers.BenefitsAn international community bringing together more than 110 different nationalitiesAn environment where trust is central: 70% of our leaders started their careers at the entry levelA strong training system with our internal Academy and more than 250 modules availableA dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.J-18808-Ljbffr","company":"Amaris Group","rawCompany":"amaris group","city":"Toronto","state":"ON","isRemote":false,"isActive":false,"createdAt":"2026-06-19T01:14:26.342Z","occupations":[{"code":"13-1082.00","title":"Project Management Specialists","slug":"project-management-specialists"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"15-1299.09","title":"Information Technology Project Managers","slug":"information-technology-project-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"541512","title":"Computer Systems Design Services","slug":"computer-systems-design-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"MES Program manager","description":"We are seeking an experienced MES Program Manager to lead and coordinate large-scale Manufacturing Execution System (MES) initiatives within a regulated pharmaceutical environment. This role requires strong program leadership capabilities, cross-functional coordination, and oversight of multiple workstreams related to MES implementation, validation, and system integration. The ideal candidate brings extensive experience managing complex programs in pharmaceutical or biotech manufacturing environments and can effectively align technical, operational, and business stakeholders to ensure successful delivery.Location & Work ModeLocation: TorontoWork Mode: HybridSeniority: Senior (7–10 years of experience)Key ResponsibilitiesLead and oversee MES programs across multiple project phases, from planning and requirements gathering through deployment and hypercareCoordinate cross-functional teams including automation, IT, manufacturing operations, validation, engineering, and qualityManage dependencies and interfaces between MES and connected systems such as PLCs, SCADA, historians, and ERP platformsEnsure alignment between business objectives, technical execution, timelines, and program deliverablesOversee Computer System Validation (CSV) activities and ensure compliance with GMP and regulatory requirementsMonitor program scope, budget, risks, timelines, and resource allocation while providing regular status updates to leadershipDrive governance, stakeholder communication, and decision-making across multiple project streamsManage external vendors, consultants, and system integrators to ensure successful delivery of milestones and deliverablesSupport issue resolution, escalation management, and continuous improvement initiativesPromote best practices in program management, quality, compliance, and operational excellenceRequired ProfileMust-Have Qualifications7–10 years of experience managing MES programs or large-scale MES projects within the pharmaceutical or biotech industryProven experience delivering MES implementations in regulated manufacturing environmentsStrong understanding of manufacturing automation architecture, including PLCs, SCADA, MES, historians, and ERP integrationsExperience overseeing validation planning and CSV activitiesSolid knowledge of GMP regulations and compliance expectationsDemonstrated leadership experience managing multidisciplinary teams and complex stakeholder environmentsStrong program management, communication, organizational, and risk management skillsCompensationExpected Compensation Range: 100Hr-150Hr.The final compensation offered will be determined based on the candidate's level of experience, skills, and qualifications, in compliance with applicable pay transparency requirements.Canadian Experience Requirement: No Canadian work experience is required for this position. Candidates are encouraged to apply regardless of previous Canadian experience.Artificial Intelligence (AI) Disclosure: No Artificial Intelligence (AI) tools are used in the screening, assessment, or selection of candidates for this position. All stages of the recruitment process are conducted by human recruiters and hiring managers.BenefitsAn international community bringing together more than 110 different nationalitiesAn environment where trust is central: 70% of our leaders started their careers at the entry levelA strong training system with our internal Academy and more than 250 modules availableA dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.J-18808-Ljbffr","datePosted":"2026-06-19T01:14:26.342Z","dateModified":"2026-06-19T01:14:26.342Z","hiringOrganization":{"@type":"Organization","name":"Amaris Group","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Toronto","addressRegion":"ON","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"7fdb83c87dcf2bcaacbbb5ed"},"url":"https://jobsearcher.com/jobs/7fdb83c87dcf2bcaacbbb5ed"}}