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Software Project Leader H/F

Post on:

Thursday, October 10th

Place:

Montpellier (France)

When:

Asap

Contract type:

CDI

 

 

  • Education: MSc. in Engineering/Science or equivalent
  • Experience: 3+ years of experience as project manager leading software teams
  • Desired experiences: Experience with Agile software development methodology

Job Summary

Software Project Leader H/F

Quantum Surgical is looking for a Software Project Leader to join a team of creative and energetic engineers who are building the next generation of smart tools for minimally invasive therapies.

The Software Project Leader is directly responsible for the successful delivery of Quantum Surgical product development projects. He/she will handle the planning, coordination and leadership of the software development activities throughout the product development lifecycle. The position includes establishing and driving project schedules, requirements, budgets, reviews, issue escalation, and responsibility for project deliverables following good design control practices.

The candidate should have demonstrated experience with product development in an industrial environment.

 

 

Key Responsibilities
  • Lead, plan and coordinate product development activities throughout the lifecycle, from user needs definition to industrialization and validation
  • Create and maintain detailed project plans with work breakdown, deliverables, milestones, resources and responsibilities
  • Lead, motivate and provide day-to-day direction to the project team to ensure on time delivery
  • Organize and lead weekly project meetings to track progress, manage risk and anticipate any impact on the plan
  • Provide timely and accurate information to management
  • Work with Marketing and Clinical to establish the product technical requirements
  • Work with Software teams to identify and anticipate the main technical risks, establish the software requirements and deliver quality products on time
  • Work with Risk and Clinical engineers to ensure the proper implementation of risk management & usability engineering activities
  • Create and maintain an accurate design history file (DHF)
  • Support the NPI & manufacturing teams in establishing the device DMR
  • Support the RA team in establishing the regulatory filings (CE, 510k, etc.)
  • Follow all applicable regulatory standards and quality procedures

 

Experiences and Qualifications
  • MSc in Engineering/Science or equivalent
  • 3+ years of experience as project manager leading software teams
  • Familiar with design controls in a CE/FDA regulated environment
  • Ability to communicate effectively and build relationships with internal/external stakeholders
  • Excellent organization and communication skills
  • Strong team player

 

Desired Experiences
  • Experience with Agile software development methodology
  • Experience developing software-controlled medical electrical equipment

 

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