Regulatory Affairs Professional
7 days ago
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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