Medical Devices Surveillance Professional

1 day ago

Galway, Galway, Ireland beBeeRegulatory Full time €50,000 - €62,000
Medical Devices Surveillance Program Specialist

We are seeking a highly skilled Medical Devices Surveillance Program Specialist to join our team. As a key member of our surveillance program, you will be responsible for ensuring compliance with government regulations and developing protocols for adverse report intake, evaluation, and follow-up.

About the Role:

  • Manage and maintain the company's medical devices surveillance program, ensuring compliance with regulatory requirements.
  • Analyze clinical databases to extract adverse event data and integrate it into a unified database system.
  • Collaborate with stakeholders to develop programs and processes for regulatory reporting requirements.
  • Lead assigned projects from design to implementation, adhering to policies and utilizing specialized knowledge.

Responsibilities:

  • Develop and implement surveillance protocols to ensure timely detection and reporting of adverse events.
  • Collaborate with cross-functional teams to identify and mitigate risks associated with medical devices.
  • Provide technical support and guidance to internal stakeholders on surveillance-related matters.
  • Stay up-to-date with changing regulatory requirements and industry best practices.

Qualifications:

  • Bachelor's degree in a related field such as healthcare, science, or engineering.
  • Minimum 3 years of experience in medical devices surveillance or a related field.
  • Excellent analytical, communication, and project management skills.
  • Ability to work independently and collaboratively as part of a team.

Benefits:

  • Opportunity to work with a dynamic team of professionals.
  • Competitive salary and benefits package.
  • Ongoing training and development opportunities.

How to Apply:

  1. Review the job description and requirements carefully.
  2. Submit your application, including your resume and cover letter, to [insert contact information].
  3. Participate in a thorough interview process, which may include technical assessments and scenario-based questions.

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