Project Manager R&D

  • Permanent
  • Geneva

Missions:

  • Contribute to the design & development of new products
  • Coordinate simultaneously several complex projects
  • Interact with the Organization (MKT, OPS, RA/QA) at the different stages of the projects from design inputs to Product Launch
  • Contribute to the maintenance of existing product ranges
  • Comply with applicable regulatory requirements ISO 13485, 21CFR Part 820 and MDR 2017/745 (EU)

You will  be in charge of:

  • Establishing and validating the design inputs
  • Executing or supervising the design & drawings of new products according to the design specifications, costs objectives, performance, and quality standards
  • Creating and monitoring the project planning
  • Checking and managing the engineering drawings
  • Being responsible for prototyping and manufacturing of test devices in conjunction with internal & external manufacturers
  • Establishing the test plan, execute or monitor the tests
  • Contributing to the design transfer of new products
  • Writing the documentation, conduct Risk Analysis and Design Verification/Validation Master Plan, in accordance with Regulatory and Quality requirements
  • Building and maintaining the Design History File (DHF) relative to the project
  • Supporting to Regulatory Affairs and Product Quality (including non-Conformity analysis); Operations and Process Validation; Marketing

 

Profile:

  • Mechanical Engineering degree or equivalent
  • 5 years min. as R&D Project Manager
  • Experience required in MD for Spine, or Orthopedic, or any other medical device industries
  • Ability to use SolidWorks
  • Computer skills (Word, Excel, PowerPoint, Teams, etc…)
  • Written and oral fluency in French and English
  • Ability to manage multiple responsibilities and tasks simultaneously, and to work autonomously
  • Solution oriented, team player, good communication skills
  • Ability to meet deadlines and to prioritize work