Regulatory Affairs Professional

7 days ago


Malmo, Skåne, Sweden g2 Recruitment Full time
About This Opportunity

This is an exciting opportunity for a Quality Management Specialist to join g2 Recruitment's team. As a Quality Engineer, you will be responsible for ensuring the quality and compliance of medical devices developed for drug delivery systems.

Main Responsibilities:
  • Evaluate and implement quality management systems.
  • Develop and maintain quality procedures and documentation.
  • Conduct internal audits and provide recommendations for improvement.
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements.
  • Stay up-to-date with changing regulatory landscapes and industry developments.

The ideal candidate will have a strong background in quality engineering and a passion for delivering high-quality solutions.

Requirements:
  • Bachelor's degree in Engineering or a related field.
  • 3+ years of experience in quality engineering (medical device or pharma).
  • Knowledge of ISO 13485, FDA regulations, and risk management.
  • Excellent communication and problem-solving skills.


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