Senior Program Manager

Job Title

Senior Program Manager

Operations

VP, Global Operations

Miami, US

The Sr. Program Manager will be accountable to create and track the project timelines, resourcing and project risks & mitigations by leading cross‑functional teams in the production of medical devices to consolidate manufacturing operations, ensuring compliance with regulatory requirements, quality standards, and business objectives. This role bridges R&D, operations, quality, clinical, regulatory and supply chain to deliver seamless product launches and scale‑up activities.

• Lead and implement a company‑wide, standard approach for project management.
• Create and manage the overall active project portfolio for the company.
• Drive Project Success:
  Assign tasks, responsibilities, and accountability to team members to create and execute project plans in accordance with policies and practices.
• Prioritize tasks and delegate when appropriate.
• Exhibit excellent time management skills with a proven ability to meet deadlines.
• Utilize Six Sigma, Lean, and other process improvement methodologies to enhance process performance.
• Work closely with cross‑functional team members including R&D, Operations, Quality, Regulatory, Sales, and Marketing teams to support the transition of new products from development to manufacturing and commercial launch.
• Prepare and present updates for ongoing projects, process improvement initiatives and project status to management.
• Lead and participate in product transfer and process improvement projects, ensuring timely and successful completion.
• Manage cost, schedule and performance to meet project objectives.

• Bachelor’s degree in Engineering or a related field.
• 8+ years of experience in medical device project management, manufacturing, product development, or technology transfer.
• Proven experience as a Project Manager in the Class III medical device industry.
• Strong knowledge of manufacturing processes, equipment, and technologies specific to medical devices.
• Familiarity with FDA regulations, design controls, clinical trials, ISO 13485, and other industry standards.
• Proficiency in process improvement methodologies (Six Sigma, Lean, etc.).
• Excellent analytical, problem‑solving, and project management skills.
• Strong communication and interpersonal skills, with the ability to work effectively in a team environment.
• PMP and/or Sigma Six (Green/Black Belt) Certification preferred.

Mid‑Senior level

Full-time

Project Management and Information Technology

Medical Device