Job description / Role
My Client is a multi-national innovative company that is very reputable in the Pharmaceutical Industry. They will be going through a change to adapt to the new situations that are going on right now. This gives you a chance to prove yourself and how efficient you can really be. After all, hard work always pays off.
Where do you fit in you may ask?
You will be working as Regulatory Affairs Specialist and you will be working on adapting with those changes. You will have a transformation project and take up all the necessary actions internally; we are talking about the local business, project team and supply chain. Also, externally which means involvement with the SFDA (Saudi Food and Drug Authorities) and you will be under supervision of a Regulatory Affairs Manager in Saudi Arabia.
What you will be expected to do is the following:
Update the local regulatory affairs system within 48 hours once the new certificate is issued.
Update the local supply chain system within 24 hours once the new certificate is issued.
Meeting all the phases deadlines for each and every single task you are given.
What you will be required to have is no less than a 1 year experience in the medical registration field.
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.