Program Manager – Medical Device

Freudenberg Group

Program Manager overseeing product development cycles and managing cross-functional teams in the medical device sector. Ensuring compliance and driving process optimization for efficient project execution.

Posted 7/6/2026full-timeBeverly • California, Massachusetts • 🇺🇸 United StatesSeniorLead💰 $120,000 - $140,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Project Management within the Medical Device industry, focusing on engineering processes, compliance with ISO standards, and the application of Lean/Six Sigma methodologies. Proven ability to lead cross-functional teams, manage complex projects, and optimize processes for cost reduction and efficiency.

Highest-signal resume keywords

Project ManagementMedical Device ManufacturingLean/Six Sigma ToolsISO 13485 ComplianceEngineering Problem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementEngineering ProcessesStatistical Problem-SolvingBudget DevelopmentProcess OptimizationDesign DocumentationGMP PrinciplesSilicone Material KnowledgePlastics ExtrusionsKPI Measurement

Soft Skills

Team LeadershipMentoringCollaborationCommunicationStakeholder Alignment

Industry Keywords

Medical DeviceISO 14001ISO 14971Manufacturing EnvironmentCross-Functional Teams

About the role

Key responsibilities & impact

Direct cross-functional internal teams, external vendors, suppliers, and strategic partners.
Build team ownership and commitment to projects and assign clear authority, accountability, and deliverables.
Drive all phases of the product development cycle.
Develop and monitor project budgets, internal billing, and TCOGS.
Maintain alignment with clinicians, customers, internal teams, and FM key stakeholders.
Identify constraints and risks, maintain credible schedules, align with CCPM/PCE practices.
Measure, report and improve program KPIs, demonstrate cost reduction through process optimization.
Develop and maintain compliant design/process documentation.
Mentor and support engineering staff development while fostering a high-performing, collaborative project culture.
Evaluate new business opportunities and lead quoting and proposal development.

Requirements

What you’ll need

Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.
8+ years’ experience in Medical Device or related industry.
6+ years’ experience in Project/Program Management in a manufacturing environment.
Prior experience with silicone material, plastics, and/or extrusions.
In-depth understanding of engineering and manufacturing processes used in medical device production.
Advanced experience with engineering/statistical problem-solving methodologies.
Deep understanding of ISO standards, particularly ISO 13485, ISO 14001, ISO 14971.
Knowledge of GMP principles and their application in medical device manufacturing.
Demonstrated experience using Lean/Six Sigma tools.
Demonstrated experience providing leadership and managing full development programs or multiple projects of high complexity.

Benefits

Comp & perks

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