
Global Product Quality Project Manager
1 day ago
We are seeking a skilled Project Manager to join our Global Product Quality team on a 12-month maternity leave cover.
This exciting opportunity is ideal for a highly motivated senior engineer looking to grow into project management, or for experienced project managers who thrive on navigating complexity, building cross-functional alignment, and driving continuous improvement in a global medical device environment.
Job SummaryAs a Project Manager – Global Product Quality, you will lead high-impact projects that ensure the safety, performance, and quality of our products worldwide.
Key Responsibilities- Manage complex, competing needs between internal groups across Quality, Regulatory Affairs, Product, Engineering, Clinical and Supply Chain to achieve optimal solutions for the business.
- Lead and coordinate cross-functional teams to resolve complex product quality challenges and achieve optimal outcomes for the business.
- Coordinate and develop formal responses to post-market requests received 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 that enhance risk management, efficiency, and product lifecycle excellence.
- Mentor and coach others, fostering a collaborative and positive team environment.
- Initiative and flexibility in managing rapidly evolving quality problems where data and outcomes are often unclear.
- 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.
- A results-driven mindset with the ability to balance competing priorities and manage risks.
- Proven project management skills, including planning, organization, delegation, and risk management.
- Excellent communication and stakeholder management skills across multiple time zones, locations, and levels.
- A passion for improving processes and systems and making a difference to patients and customers.
- 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, MDR) or the ability to rapidly learn and apply them.
Join us and be part of a diverse and inclusive culture that encourages individual expression in the workplace and thrives on innovative ideas. We offer a supportive and inspiring work environment that helps you not only meet your goals but also create new ones.
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