Regulatory Affairs Vacancy At GSK Egypt
Vacancy title: Regulatory Specialist Assembly
Job Description:
Are you looking for a regulatory affairs role that will enhance your documentation knowledge and allow you to help shape systems strategy? If so, this Regulatory Affairs Operations role could be an exciting opportunity to explore.
As a Regulatory Affairs Operations Staff, you will assemble, link and publish submission packages that meet Regulatory Authority technical standards and GSK requirements and schedules.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
– Deliver of Complex submission packages independently, to agreed schedule and technical specification.
– Check compliance of other’s work with requirements and standards.
– Advise and assist authors with more complex or non-routine preparation or document management procedures.
– Support submission team review and approval procedures.
– Maintain knowledge of relevant regulatory authority rules and GSK standards associated with submission format.
– Lead the creation and implementation of publishing working practices and procedures aimed at simplifying processes and increasing quality.
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Bachelor’s degree in pharmacy
2-3 years relevant previous working experience
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
– Service Orientation
– Ability to work carefully under time constraints.
– Good team worker.