Project Manager

6 giorni fa

Padova, Veneto, Italia Page Personnel A tempo pieno
Job Description

We are seeking a highly skilled Project Manager to join our team in Italy near Padova. As a key member of our organization, you will be responsible for overseeing and managing all aspects of new product development and product change projects from initiation to launch.

Key Responsibilities
  1. Project Planning and Strategy
  • Develop comprehensive project plans to ensure timely and within-budget execution.
  • Collaborate with stakeholders to establish project scope and milestones.
  • Identify project risks and develop strategies to mitigate them.
Project Execution, Monitoring and Control
  • Lead cross-functional, international, and multi-site teams to achieve project objectives.
  • Monitor project progress, identify bottlenecks, and take corrective actions to keep projects on track.
Project Closure
  • Ensure the overall scope of the projects, its objectives, and deliverables are ready for successful launch.
Quality Assurance and Regulatory Compliance
  • Collaborate with regulatory affairs and quality assurance teams to ensure compliance with applicable regulations, standards, and guidelines.
  • Implement design controls and risk management processes to ensure safe and effective medical devices and medical software releases.
Stakeholder Engagement and Collaboration
  • Build strong relationships with stakeholders, promote collaboration, and manage expectations.
  • Effectively communicate project progress, risks, and issues to stakeholders at various levels.
Continuous Improvement
  • Conduct post-project evaluations, review, and formulate lessons learned for future projects.

Requirements

  • Proficiency in English (level C2) with excellent communication and presentation skills.
  • Proven experience (minimum 5 years) in managing medical device (and/or medical software) development projects.
  • Strong knowledge of medical device development processes, including design controls, risk management, and regulatory requirements.
  • Excellent project management skills, including planning, execution, and monitoring with a focus on prioritization and meeting deadlines.
  • Leadership abilities, with a track record of successfully leading and motivating cross-functional teams.
  • Excellent communication, negotiation, and stakeholder engagement skills.
  • Strong analytical skills and the ability to manage systematically the changing project requirements.
  • Attention to detail and ability to manage multiple interrelated projects simultaneously.
  • Knowledge of relevant regulations and standards, such as FDA regulations (e.g., 21 CFR Part 820), ISO 13485, and ISO 14971. Knowledge about clinical trials would be beneficial.
  • Project management certifications (e.g., PMP) are highly desirable.
  • Proficiency in project management tools and software.

What We Offer

  • A meaningful role contributing to people's eye health and quality of life.
  • An opportunity to work for a growing, successful, and international publicly listed company.
  • A chance to have a key role in the development of new medical solutions to support the growth and expansion of the business.

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