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Regulatory Affairs and Quality Management Specialist

vor 3 Monaten


Bochum, Nordrhein-Westfalen, Deutschland Atlas medical Technologies GmbH Vollzeit

ATLAS medical technologies GmbH is an innovative enterprise focused on the development and distribution of advanced navigation systems for healthcare professionals in the fields of interventional radiology and orthopedics. Our cutting-edge 4D laser navigation technology enhances operational efficiency and facilitates more accurate instrument guidance, resulting in gentler, shorter, and reduced radiation exposure treatments for patients.

Key Responsibilities
  • Developing, reviewing, and sustaining technical documentation in compliance with the Medical Device Regulation (MDR) for Class I and IIa medical devices.
  • Strategizing, gathering, and executing regulatory obligations and approval standards within the EU and on an international scale.
  • Engaging with notified bodies and regulatory authorities.
  • Preparing documentation tailored to specific country requirements for product approvals.
  • Conducting market surveillance for medical devices.
  • Supporting the maintenance and enhancement of the Quality Management System (QMS) in alignment with ISO 13485:2016 and EU-MDR 2017/745, as well as FDA CFR 21 Part 820.
  • Fostering awareness and providing training to staff regarding regulatory obligations.
  • Planning, executing, and assessing both external and internal audits, while also assisting in development projects and feasibility assessments.
Qualifications
  • A degree in Regulatory Affairs or Quality Management, accompanied by a minimum of 3 years of experience in regulatory affairs or quality management (ISO 13485, CFR 21 Part 820, MDR, MDD).
  • Knowledge of FDA approval processes; experience as a Quality Manager or Regulatory Affairs Manager in a startup setting is advantageous.
  • Proficient in written and spoken English, with strong skills in MS Office applications.
Benefits
  • Diverse and engaging responsibilities within a dynamic medical technology startup environment.
  • Opportunity to contribute to the evolution of healthcare solutions.
  • Competitive compensation and adaptable working arrangements.
  • Potential for professional growth within Quality Management.

We are eager to receive your comprehensive application and potentially welcome you to our team.