We need an expert in regulatory affairs for medical devices in Morocco, who can provide detailed, in-depth reports on the local regulatory frame, and who can act as a link between our company and the regulatory authority.
The required deliverables depend on the country regulatory framework, which could be:
- regulatory strategy and intelligence reports
- evidence of regulatory submissions
- regulatory approval of the product
Some of the activities involved are:
- compile, write and edit regulatory reports
- provide advice and rational interpretation on regulatory strategies
- interact with the competent authority and provide written and oral feedback about contacts and processes
- research specific regulations and their implementation
- clarify specific doubts on not-formalized practical procedures (i.e. importation scheme)
The expert should have a relevant degree such as biochemistry, biotechnology, pharmacy, medicinal chemistry, biomedical science, or life applied science.
Key skills:
- analytical thinking
- time management
- problem-solving skills
- communicational skills
- excellent oral and written English is mandatory
About the recuiterMember since May 20, 2018 Andrew Djuwidja
from Veracruz, Mexico