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OSI Systems

Diversified tech company spanning security, healthcare

Senior Program Manager

Program ManagementPosted on Nov 10
Full-timeEdinburgh, UKNo salary listed

About the Job

Requirements

  • A Bachelor of Science degree in Engineering, Computer Science, or a similar related degree.
  • At least 5 years of experience in related research and development roles, including program or project management, test or verification and validation, or operations engineering.
  • At least 3 years of experience managing complex development projects within demanding timeframes.
  • Practical experience delivering products under medical-device design controls and quality-system requirements, including applicable United States and European regulatory frameworks.
  • A solid understanding of the development process, including requirements gathering, analysis and design, development tools and technologies, release and version control, contemporary testing methodologies, and deployment management.
  • The ability to deliver results through others in direct and matrixed organizational models.
  • The ability to attend global meetings and work global hours as needed.
  • The ability to travel internationally and acquire all necessary travel documents; travel may be up to 10%.

Responsibilities

  • Manage and ensure the successful delivery of high-impact programs.
  • Build, drive, and support cross-functional project teams, including research and development, service, marketing, regulatory, quality, clinical, supply chain, and manufacturing.
  • Lead cross-functional teams in delivering new and sustaining products, including integrated software and hardware platforms and cloud services; ensure software architecture and hardware capabilities remain aligned so solutions are robust and scalable.
  • Manage program scope, schedule, budget, and risk to ensure product delivery on time, on budget, and to quality standards.
  • Establish and maintain the integrated program plan, including development, design control, regulatory, verification and validation, design transfer, commercial launch, and sustaining activities; ensure formal review and phase-gate entry and exit criteria are defined, evidenced, and met.
  • Generate, communicate, coordinate, and manage Medical Device File deliverables consistent with Quality Management System processes.
  • Lead by example and cultivate continuous learning and development to enhance team skills and performance.
  • Coordinate tasks and project deliverables across internal and external contract resources.
  • Create and maintain tools and frameworks to track projects, escalate issues, and drive resolution; provide clear project updates to the cross-functional team and senior leadership.
  • Negotiate schedule, risk, product-feature, and resource trade-offs with project and program teams.
  • Provide evidence-based program reporting and lead formal program reviews with cross-functional teams and senior leadership, communicating status, forecasts, risks, decisions, and required support.
  • Ensure team members, including direct or indirect reports, are trained and evaluated on knowledge of and adherence to company values, the Code of Ethics and Conduct, and applicable compliance policies.
  • Report quality problems or defects to a manager or senior management member so corrective action can be implemented and recurrence avoided.

About the Company

OSI Systems

Diversified tech company spanning security, healthcare

OSI Systems operates three divisions: Security, Healthcare, and Optoelectronics and Manufacturing. The Security division supplies inspection systems for airports, ports, and borders that scan people and cargo using imaging and sensors. The Healthcare division produces patient monitoring and diagnostic equipment, while the Optoelectronics division makes electronic components for various devices. The company differentiates itself through its diversified, three-pronged portfolio and growth via acquisitions like Rapiscan and Spacelabs; its goal is to deliver technology-enabled solutions that protect people and infrastructure, support clinical care, and provide high-quality components.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Hawthorne, CA
Founded
1987

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