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Regulatory Affairs Professional for Medical Devices

1 mese fa


Milano, Lombardia, Italia Page Personnel A tempo pieno

Page Personnel is seeking a highly skilled Regulatory Affairs Specialist to play a key role in ensuring compliance with regulatory requirements for our medical devices. The ideal candidate will have a strong understanding of FDA regulations, EU Medical Device Regulation (MDR), and international regulatory requirements for medical devices.

About the Role

We are looking for an experienced Regulatory Affairs Specialist to join our team. This individual will be responsible for preparing and submitting regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design Dossiers, and other regulatory filings as required.

Key Responsibilities
  • Prepare and submit regulatory submissions to regulatory authorities, including 510(k) premarket notifications, Technical Files, Design Dossiers, and other regulatory filings as required.
  • Maintain regulatory files and documentation in accordance with regulatory requirements and company procedures.
  • Review and interpret regulatory requirements and guidelines to ensure compliance with relevant regulations and standards, including FDA regulations (21 CFR Part 820), ISO 13485, and other applicable standards.
  • Support regulatory assessments for new product development projects, including regulatory strategy development, risk assessments, and regulatory impact analyses.
  • Monitor changes in regulations, standards, and guidance documents related to medical devices and communicate updates to relevant stakeholders.
  • Support post-market surveillance activities, including adverse event reporting, field corrective actions, and regulatory reporting requirements.
Requirements
  • Master's degree in Biomedical engineering or relevant discipline.
  • Minimum of 3 years of experience in regulatory affairs within the medical device industry.
  • Experience with Class II or Class III medical devices, implantable device experience is a plus.
  • Knowledge of quality management systems and ISO 13485 requirements.
  • Strong understanding of FDA regulations, EU Medical Device Regulation (MDR), and international regulatory requirements for medical devices.
  • Excellent written and verbal communication skills, with the ability to effectively communicate complex regulatory requirements to cross-functional teams.
  • Detail-oriented with strong organizational skills.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Fluent in English, written and spoken.
What We Offer

The salary for this position is approximately $110,000 per year, based on industry standards and location considerations. As a valued member of our team, you will also receive a range of benefits, including:

  • A comprehensive benefits package.
  • Ongoing training and professional development opportunities.
  • A supportive and collaborative work environment.
  • The opportunity to work on exciting and challenging projects.

RA Specialist Medical Devices - Page Personnel