Program Manager

Program Manager – Medical Device Industry

An exciting opportunity exists for an experienced Program Manager to lead strategic initiatives within the medical device sector. In this role, you will manage cross-functional teams to deliver innovative healthcare solutions from concept through to regulatory approval and commercialization. The ideal candidate will bring technical expertise, leadership, and a solid understanding of the medical device lifecycle, quality, and regulatory requirements.

Responsibilities Include but are not Limited to:

• Program Leadership: Manage multiple complex programs across the full medical device development lifecycle—from ideation through design, testing, and regulatory approval—aligned with strategic business objectives.

• Cross-Functional Collaboration: Work closely with product development, engineering, quality assurance, regulatory affairs, and commercial teams to drive seamless program execution.

• Stakeholder Engagement: Communicate progress, risks, and key milestones clearly to senior leadership and stakeholders. Set and manage expectations across all teams.

• Regulatory Compliance: Ensure all projects comply with global regulatory standards (FDA, CE, ISO). Manage required documentation, testing, and approvals for successful market entry.

• Quality Oversight: Champion quality assurance processes to ensure products meet the highest industry standards, regulatory expectations, and patient needs.

• Resource & Budget Management: Allocate resources across multiple projects efficiently, monitor budgets, and ensure on-time delivery.

• Process Optimization: Drive continuous improvement in internal workflows, tools, and project methodologies to enhance quality and speed of delivery.

• Team Leadership: Mentor and lead cross-functional teams, fostering collaboration, accountability, and high performance.

Program Leadership: Manage multiple complex programs across the full medical device development lifecycle—from ideation through design, testing, and regulatory approval—aligned with strategic business objectives.

Cross-Functional Collaboration: Work closely with product development, engineering, quality assurance, regulatory affairs, and commercial teams to drive seamless program execution.

Stakeholder Engagement: Communicate progress, risks, and key milestones clearly to senior leadership and stakeholders. Set and manage expectations across all teams.

Regulatory Compliance: Ensure all projects comply with global regulatory standards (FDA, CE, ISO). Manage required documentation, testing, and approvals for successful market entry.

Quality Oversight: Champion quality assurance processes to ensure products meet the highest industry standards, regulatory expectations, and patient needs.

Resource & Budget Management: Allocate resources across multiple projects efficiently, monitor budgets, and ensure on-time delivery.

Process Optimization: Drive continuous improvement in internal workflows, tools, and project methodologies to enhance quality and speed of delivery.

Team Leadership: Mentor and lead cross-functional teams, fostering collaboration, accountability, and high performance.