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Regulatory Compliance Specialist

vor 2 Monaten


Deutschland Melio Life Science Vollzeit
Department Head - Quality Management, Regulatory Affairs & Product Development

We are seeking a highly experienced Department Head to lead our Quality Management, Regulatory Affairs & Product Development department. As a key member of our team, you will be responsible for ensuring the highest standards of quality and regulatory compliance in our medical device products.

Key Responsibilities:
  • Lead and inspire an interdisciplinary team of experts in quality management and regulatory affairs.
  • Oversee and continually improve our Quality Management System (QMS) in compliance with international standards.
  • Develop and implement risk management strategies to ensure regulatory compliance.
  • Drive efficiency and transparency by implementing automated, software-based systems to enhance compliance.
Requirements:
  • Degree in medical technology, engineering, natural sciences, or a related field.
  • Extensive experience in quality management and regulatory affairs within the medical device industry.
  • Fluent in both German and English.
What We Offer:
  • A dynamic work environment where you can drive innovation.
  • Opportunities for professional growth and career development.
  • Competitive salary and benefits.
  • The chance to work with cutting-edge medical technologies in an international market.