Senior Manager Medical Device Project Leader

CHF130000 - CHF150000 per annum
  1. Permanent
Nyon
  1. Clinical Operations, Project Management
Posted: 27/05/2020
BBBH14054

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Hobson Prior are working with a world-wide healthcare organisation whose products and services are used to help care for patients who are critically ill. Our client is looking for a Senior Manager Medical Device Project Leader to join them on a permanent basis in Nyon, Switzerland.


Job Responsibilities:

  • Responsible to lead cross-functional exercises to define targeted device profiles.
  • Deliver quality products and processes with appropriate validation and regulatory documentation.
  • Develop device development project plans and budget with internal and external cross functional teams.
  • Report and tightly control device development timelines, budget and risks to biosimilars project development team.
  • Act as the main interface between the biosimilars project development teams and the subteams (e.g. medical devices, manufacturing & supply, etc.) as well as device vendors.
  • Deliver technical and business inputs to projects. Analyze risks and suggest mitigation plans.
  • Oversee device development, manufacturing, validation and regulatory activities.
  • Proactively anticipate and identify risk areas and alert stakeholders appropriately.
  • Report and escalate to management potential issues as needed.
  • Recognise new device opportunities.

Key Skills:

  • Solid organizational skills including attention to detail and multi-tasking skills.
  • Effective verbal and written communication.
  • Fluent in English, both oral and written; additional languages (German or French) are an asset.
  • Strong interpersonal and relationship building skills with the ability to establish a trusted role with the various stakeholders.

Requirements:

  • Bachelor's degree (or equivalent) in an applicable Product design, Mechanical, Process, Materials Science or Electronic Engineering field.
  • 5+ years of experience in project management
  • 5+ years of experience in device development with an understanding of device safety, regulatory requirements, policies and procedures.
  • Deep technical understanding of device design, validation, verification and their link to other drug development activities (clinical, manufacturing, commercial, etc.) in the overall drug development plan.
  • Experience in FDA regulated medical devices, standalone CE marked devices and combination drug device products.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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