Programme Manager

4 weeks ago

London, Greater London, United Kingdom SAVA Full time
Job Overview

Sava is a leading innovator in biosensing technology, and we are seeking a skilled Programme Manager to oversee the development lifecycle of our medical devices. This role requires a unique blend of technical insight, project management proficiency, and leadership capabilities to drive cross-functional teams towards successful product launches.

Key Responsibilities
  • Define and manage project scopes, strategies, budgets, and schedules for multiple, simultaneous projects, working closely with cross-functional teams.
  • Lead programme planning, resource allocation, and scheduling to ensure alignment across all departments and adherence to timelines.
  • Act as the primary point of contact for project updates, ensuring stakeholders are informed on project progress, risks, and issues.
  • Facilitate cross-functional problem-solving and drive collaboration to address project challenges and ensure alignment with business objectives.
  • Collaborate with the Heads of Departments and Team Leads to balance resources, deliverables, and business priorities, ensuring optimal team performance.
  • Conduct regular project review meetings, identify bottlenecks, and implement solutions to keep projects on track.
  • Establish and monitor Key Performance Indicators (KPIs) to assess project performance and proactively identify areas for improvement.
  • Support project execution by maintaining a focus on project goals and objectives, adapting project plans as needed in response to changes in scope or business priorities.
  • Drive the adoption of best practices in project management, including documentation, risk management, and reporting.
Requirements
  • A minimum of 5 years of project or programme management experience in a regulated environment.
  • Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or a related field.
  • In-depth understanding of medical device regulations, including FDA 21 CFR Part 820, ISO 13485, and CE marking requirements.
  • Proven track record of successfully managing complex medical device development projects throughout the development lifecycle.
  • Experience in development during Design for Manufacture and an understanding of manufacturing processes.
  • Demonstrated ability to lead cross-functional teams, manage multiple projects simultaneously, and drive projects to successful completion.
  • Excellent verbal and written communication skills, with the ability to present complex information clearly and concisely to diverse audiences.
  • A 'figure it out' attitude when navigating challenges, driving to effective solutions.
  • Proficient in project management tools (e.g., JIRA, Confluence) and Microsoft Office Suite.
  • You have worked on projects focussing on CGM or diabetes-related technologies.
  • You may have certification for PMP, PRINCE2, or other project management qualifications.

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