2 дня назад
Lead Project & Program Manager: Delivery and Portfolio Office Enablement and Medical Device Enablement (Medical Devices)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Lead Project & Program Manager: Delivery and Portfolio Office Enablement and Medical Device Enablement (Medical Devices): Leading cross-functional programs that improve the development, launch, and sustainment of medical device products with an accent on quality systems, regulatory readiness, governance, and operational excellence. Focus on building integrated plans, managing risks and dependencies, driving QMS transformation, and enabling adoption of new processes across a complex matrix organization.
Location: London, United Kingdom — Canada Square; onsite role
Company
Health provides professional information, software, and services for healthcare and regulated industries.
What you will do
- Lead a portfolio of medical device enablement programs across Operations, Quality, Regulatory Affairs, Clinical, Product, Commercial, and Technology.
- Build and maintain integrated project plans covering scope, timelines, governance, resources, risks, dependencies, and success metrics.
- Drive Quality Management System migration, enhancement, and optimization, including organizational readiness, training, and user adoption.
- Coordinate cross-functional planning, requirements gathering, prioritization, decision-making, and issue resolution.
- Prepare executive reporting, portfolio updates, risk assessments, and decision-support materials for senior leadership.
- Improve governance, execution discipline, handoffs, change adoption, and operational readiness across the medical device lifecycle.
Requirements
- Significant experience leading complex project and program management initiatives in large, cross-functional, matrixed organizations.
- Experience delivering business transformation, operational excellence, or enterprise change programs.
- Experience in regulated industries such as medical devices, life sciences, healthcare, or pharmaceuticals.
- Proven ability to manage integrated plans with multiple workstreams, stakeholders, dependencies, budgets, risks, and competing priorities.
- Strong stakeholder management, communication, presentation, facilitation, organizational, and executive communication skills.
- Practical understanding of Agile methodologies and their application in business and operational environments.
Nice to have
- Project Management Professional (PMP) certification.
- Experience with medical device development, quality systems, regulatory compliance, or product lifecycle management.
- Experience leading Quality Management System implementations, migrations, or transformation programs.
- Agile certification such as Scrum Master, SAFe, or AgilePM.
Culture & Benefits
- Work in a complex matrix organization with global teams, executive stakeholders, and third-party vendors.
- Collaborate across Quality, Regulatory Affairs, Clinical, Operations, Product, Commercial, and Technology functions.
- Focus on accountability, collaboration, continuous improvement, and operational excellence.
- Participation in an in-person interview process may be required at a office.
Hiring process
- Interviews are conducted without AI tools or external prompts and may include in-person participation at a office.
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