The Manufacturing Program Manager will lead complex, global manufacturing programs involving new or modified medical devices and drug-device combination products. The role focuses on program strategy, execution planning, cross-functional coordination, risk management, manufacturing readiness, product transfers, and commercial product launches.
The successful candidate will coordinate activities across Manufacturing, Engineering, Science & Technology, Supply Chain, Quality, and Regulatory teams to ensure programs meet established milestones, budgets, and business objectives.
This is primarily a program management and coordination role, rather than a hands-on technical engineering or product design position.
Responsibilities:
Define and document program scope, execution strategies, resources, deliverables, timelines, and milestones.
Lead global manufacturing programs involving assembly, labeling, packaging, testing, storage, and product release.
Develop and maintain integrated program schedules, Gantt charts, milestone plans, and work breakdown structures.
Coordinate product and manufacturing transfers from development to commercial operations.
Facilitate global kickoff meetings, governance meetings, stakeholder reviews, and cross-functional planning sessions.
Align manufacturing sites and global teams to ensure effective program execution.
Coordinate material planning, sourcing, distribution, and supply readiness across manufacturing networks.
Manage program budgets, monitor financial performance, and address budget variances.
Identify program risks, develop mitigation strategies, and implement contingency plans.
Coordinate with Quality and Regulatory teams to support regulatory submissions, product approvals, and market launches.
Track program progress, resolve execution barriers, and communicate risks and issues to senior leadership.
Prepare program charters, RACI matrices, risk registers, milestone tables, and executive presentations.
Identify opportunities to improve efficiency, reduce costs, accelerate timelines, and strengthen program governance.
Ensure proper program closeout and transition ongoing responsibilities to appropriate teams.
Required Qualifications:
Bachelor's degree in Engineering, Science, or a related discipline; an advanced degree is preferred.
10+ years of professional experience in a regulated manufacturing, medical device, engineering, or technical operations environment.
At least 5 years of global program and/or project management experience.
At least 5 years of relevant experience in device manufacturing, combination product packaging, or a closely related manufacturing environment.
Demonstrated experience with combination product assembly, labeling, packaging, qualification, and industrialization.
Experience managing product transfers from development to manufacturing operations.
Experience with new product introduction (NPI), manufacturing readiness, and product launches.
Strong understanding of cross-functional program execution, stakeholder alignment, and risk management.
Advanced proficiency in MS Excel, MS Project, PowerPoint, Teams, and SharePoint.
Excellent communication, organizational, presentation, negotiation, and leadership skills.
Ability to work effectively with senior stakeholders, including directors, vice presidents, and executive leadership.
Willingness to travel domestically and internationally as needed.
Preferred Qualifications:
PMP certification or equivalent program management credentials.
Experience with quality systems, design controls, product labeling, and regulatory submission preparation.
Knowledge of commercial supply readiness and global regulatory requirements.
Experience with Power BI, Smartsheet, and AI-enabled productivity tools.
Strong financial management skills and business acumen.
Multilingual communication skills.
Mandatory Requirements:
10+ years of experience in the medical device industry or a closely relevant regulated manufacturing environment.
Minimum 5 years of experience in global program management.
Strong experience with drug-device combination products.
Experience in medical device manufacturing, combination product assembly, labeling, and packaging.
Experience with new product manufacturing, product launches, and product transfers.
Experience coordinating global manufacturing programs across multiple sites.
Bachelor's or master's degree in Engineering or Science.
Strong knowledge of MS Excel, MS Project, PowerPoint, Teams, and SharePoint.
Ability to work onsite in Worcester, MA, Tuesday through Thursday.
Numbers & Facts
Location
Worcester, MA
Skills
Artificial Intelligence (AI)unmatched
Budget Managementunmatched
Budgetingunmatched
Business Skillsunmatched
Communication Skillsunmatched
Contingency Plansunmatched
Cost Controlunmatched
Cross-Functionalunmatched
Financial Managementunmatched
Functional Programming Languagesunmatched
Leadershipunmatched
Manufacturingunmatched
Manufacturing Assemblyunmatched
Manufacturing Managementunmatched
Manufacturing Operationsunmatched
Materials Planningunmatched
Medical Equipmentunmatched
Microsoft Excelunmatched
Microsoft PowerPointunmatched
Microsoft Projectunmatched
Microsoft SharePointunmatched
Multilingualunmatched
Negotiation Skillsunmatched
Organizational Skillsunmatched
Performance Analysisunmatched
Power BIunmatched
Product Designunmatched
Product Managementunmatched
Product Packagingunmatched
Product/Service Launchunmatched
Project Management Professional (PMP)unmatched
Project/Program Coordinationunmatched
Project/Program Managementunmatched
Regulationsunmatched
Regulatory Requirementsunmatched
Regulatory Submissionsunmatched
Riskunmatched
Risk Analysisunmatched
Risk Managementunmatched
Strategic Planningunmatched
Supply Chainunmatched
Technical Operationsunmatched
Willing to Travelunmatched
Work Breakdown Structure (WBS)unmatched
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