Regulatory Affairs Officer – Triticum – Maastricht

Triticum

Jobid=A.0.049

Company Description

In 2002, we were the first company to obtain CE certification and FDA approval for our Medical Grade Honey: L-Mesitran. Then and now, we aspire to deliver high quality products to ensure fast and efficient wound healing. We are more than just honey. We researched honey and the ways to improve this natural ingredient. As a result, we supplement our Medical Grade Honey with e.g. vitamins to be even more efficacious.

L-Mesitran products are versatile. They are extremely effective in both human and veterinary medicine. It does not only cure complex wounds, but it also removes biofilms from infected wounds which makes healing faster and efficient. L-Mesitran products can be used as an alternative or complementary therapy for antibiotics to treat and prevent local infections, including those with multi-resistant pathogens while reducing problems of antibiotic resistance. We are available in over 80 countries worldwide.

Role Description

This is a full-time on-site role as a Regulatory Affairs Officer located in Maastricht. The Regulatory Affairs Officer will be responsible for ensuring compliance with (MDR) regulations, submitting documents to regulatory agencies, and coordinating regulatory submissions and approvals.

Qualifications

  1. Strong understanding of regulatory requirements and processes
  2. Excellent attention to detail and organizational skills
  3. Effective communication and interpersonal abilities
  4. Ability to work independently and in a team
  5. Bachelor’s degree in a relevant field, such as Biology or Chemistry
  6. Previous experience in regulatory affairs is a plus
  7. Our main language is English

Seniority level

Entry level

Employment type

Full-time

Job function

Legal

#J-18808-Ljbffr

Lees hier meer

Deel deze vacature: