Global Product Assurance Professional

2 days ago

Sydney, New South Wales, Australia beBeeProject Full time $160,000 - $200,000

Role Overview:

As a Project Director – Global Product Assurance, you will lead high-impact projects that ensure the safety, performance, and quality of products worldwide.

About the Position:

  • Manage complex needs between internal groups across Quality, Regulatory Affairs, Product, Engineering, Clinical, and Supply Chain to achieve optimal business outcomes.
  • Lead cross-functional teams to resolve product quality challenges and achieve business objectives.
  • Develop formal responses to post-market requests from regulatory authorities.
  • Act as a trusted advisor and facilitator across global teams, balancing patient safety, commercial, and regulatory priorities.
  • Drive continuous improvement of Quality and Operational systems, embedding best practices for risk management, efficiency, and product lifecycle excellence.
  • Mentor and coach others, fostering a collaborative team environment.

Key Qualifications:

  • Proven project management skills, including planning, organization, delegation, and risk management.
  • Ability to influence and negotiate conflicting points of view across commercial, quality, regulatory, and product development perspectives.
  • Strong problem-solving, analytical, and conceptual thinking skills.
  • Results-driven mindset with the ability to balance competing priorities and manage risks.
  • Excellent communication and stakeholder management skills across multiple time zones, locations, and levels.
  • Passion for improving processes and systems and making a difference to patients and customers.

Requirements:

  • Degree in Engineering, Science, or a related discipline (or equivalent experience).
  • Strong background in regulated industries, ideally healthcare or medical devices.
  • Demonstrated experience leading or contributing to complex, cross-functional projects – either as a project manager or as an engineer driving project outcomes.
  • Proven ability to coordinate across multiple stakeholders and functions on challenging, multi-factorial topics.
  • Working knowledge of medical device regulations (e.g., FDA, ISO 13485) or the ability to rapidly learn and apply them.

Why Us:

We value diversity and inclusion, encouraging individual expression in the workplace and thriving on innovative ideas. If this sounds like the workplace for you, we encourage you to apply now.

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