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Guerbet is a leader in medical imaging worldwide, offering a wide range of pharmaceutical products, medical devices, digital and AI solutions for diagnostic and interventional imaging, to improve the diagnosis and treatment of patients.

A pioneer since more than 90 years in the field of contrast media, Guerbet is continuously innovating with 9% of revenue dedicated to Research & Development and four centers in France, Israel and the United States.

Guerbet (GBT) is listed on Euronext Paris (segment B – mid caps) and generated €817 million in revenue in 2019 with a global workforce of over 2,800 employees.

Achieve, Cooperate, Care and Innovate are the values that Guerbet's employees share and practice every day. Working at Guerbet means playing a unique part in the future of medical imaging. Passionate about its business, the company strive day in, day out to combine performance, quality and sustainable development.

For more information about Guerbet, please go to www.guerbet.com  and follow Guerbet on Twitter @GuerbetGroup

 

Medical Device Vigilance Manager M/F

 

Guerbet is recruiting a Medical Device Vigilance Manager M/F who will be based in Villepinte (93).

 

Reporting to the Global Head of Medical Device Vigilance Operations, you will provide a support in the assessment and risk monitoring related to our product use.

 

Key Responsibilities

 

  • Medical device vigilance cases treatment
  • Products complaint files management
  • Relationships with subsidiaries and distributors (worldwide)
  • Medical assessment of the products benefit/risk ratio
  • Contribute to the post marketing surveillance reports (PMS) drafting
  • Analyze trends related to complaints (trend analysis reports)
  • Support in the medical device vigilance database creation
  • Quality procedures updating, participation in audits and inspections
  • Medical information (manufacturers, local and European Competent Authorities)

 

Desired Profile

 

  • Holder of a Pharmacist degree, Doctor or equivalent
  • Significant experience in the medical device vigilance field
  • 5 years of professional experience or more in the medical device industry
  • Good command of international regulatory requirements on medical device vigilance
  • Ability to deal with complex and various information (both medical and technical)
  • Good interpersonal skills, excellent analytical and synthesis skills
  • Proficiency in english (written and verbal)

 

Potential travel to be expected (around 30%)