Project Manager MDR Compliance

2 days ago


Stockholm, Stockholm, Sweden TFS HealthScience Full time

As a key member of the TFS HealthScience team, you will be responsible for leading and coordinating efforts to ensure adherence to Medical Device Regulation (MDR) and related regulatory frameworks.

About This Role

This is a full-time position (1.0 FTE) in a hybrid working setting, requiring on-site presence as well as remote flexibility.

You will collaborate closely with a global sponsor dedicated to advancing innovation in biologics development.

Your primary responsibility will be to develop project plans, set goals, manage resources, mitigate risks, and ensure timely delivery within scope and budget.

  • Oversee the planning, execution, and completion of projects related to MDR compliance.
  • Develop and implement strategies to align with regulatory requirements.
  • Coordinate with cross-functional teams, including legal, quality assurance, and operations.
  • Ensure project milestones are met while maintaining high-quality standards.
  • Manage risk assessment and mitigation strategies.
  • Communicate project updates to stakeholders and regulatory bodies.

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