vor 4 Tagen

Senior Product Development - Medical devices - Canton of Vaud

  • Arbeitsregion
  • Branche
  • Anstellungsart
  • Position

Senior Product Development - Medical devices - Canton of Vaud

Senior Product Development
Medical Devices
6 months
Canton of Vaud

Lead product development projects ensuring consistency with corporate strategy, company policies, and regulations. Ensure product performance to customer/functional specifications is in balance with deadlines and budgets. This includes identifying resources and coordinating the efforts of cross-functional project team members to deliver projects according to plan.

Your responsibilities:
Lead product development projects/programs:

  • Conduct detailed project planning
  • Drive and communicate project execution with detailed timelines and action items
  • Provide project updates to project and senior leadership team on an ongoing basis
  • Identify risks/roadblocks, provide options to mitigate issues and enlist management support to resolve issues
  • Identify project resource needs and manage allocation
  • Manage approved project budget
  • Collaborate cross-functionally ensuring common focus and understanding of project goals across all functional representatives
  • Motivate team members, resolve conflict and facilitate timely decision making
  • Lead design reviews and utilize analytical skills to drive technical decision making

Your profile:

  • Bachelor of Science Engineering degree (i.e. Mechanical, Chemical, Biomedical, Physics)
  • 5+ years work experience leading product development projects
  • 3+ years technical experience in one or more areas of development of embedded software, custom electronics, custom mechanical systems and/or consumables, or verification.
  • Proficient with project management software
  • Proven track record of successfully managing large scale projects
  • Strong written and verbal communication skills and interpersonal skills to effectively translate ideas, concepts and information
  • Ability to work with different internal and external customers in a professional manner
  • Proven experience to work cross-functionally across an organization, at all levels of the organization
  • Working knowledge and experience with quality systems regulations and guidelines, ISO, cGMP, Medical Device Directive (MDD), Canadian Medical Device regulations, Japanese PAL and FDA regulatory requirements
  • Ability to travel both domestically and internationally


  • Certification in project management or equivalent
  • Advance degree in business or technology
  • Experience leading new product development projects/programs
  • Experience leading catheter/consumable projects


  • Travel requirements are expected to be less than 20%.

Votre contact Kelly
Ana Nunes
Consultant Professional Staffing Life Science
Kelly Scientific Geneva

rue du Rhône 114 1204 Vaud