Job closed
Ref: SP317-28
Job description / Role
Main Responsibilities:
- Responsible for the presentation of registration documents to regulatory agencies.
- Carry out all the subsequent negotiations necessary to obtain and maintain marketing authorisation for the products concerned.
- Review, evaluate, and compile files and reports for submission.
- Outlining requirements for labelling, storage, and packaging.
- Corresponding with the manufacturers for the Authorised Representative process.
- Detailing them the requirements for appointing the Authorised representative in Saudi Arabia.
- MDMA and MDIL
- Monitor company progress toward fulfillment of regulatory commitments.
Requirements
Profile:
- My client prefers someone who is a bio medical engineer.
- Has to be a Saudi national.
- They want someone who is motivated to work and has valid experience in the SFDA regulations and processes.
- Experience within pharmaceutical companies is a must.
About the Company
NonStop Consulting is one of the fastest-growing recruitment and staffing firms currently supporting the pharmaceutical and medical device industries across the US with expert consultants providing contingency, search and selection, contractors or labor leasing services, and managed vendor services.
As a company, we are renowned for professionalism, unrivaled industry knowledge and extensive candidate networks with the service our multinational, multilingual teams provide being underpinned by an in-house Quality Assurance team, something unique in our industry.