Job Description Summary
Job Description
We are the makers of possible
BD (Becton, Dickinson and Company) is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. Headquartered in the United States, BD has a presence in virtually every country and partners with organizations around the world to address some of the most challenging global health issues.
Why Join Us?
A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.
Become a maker of possible with us!
As a Regulatory Affairs Associate , you will be responsible for launching of Medical Device & In-Vitro Diagnostic Products in the Saudi Arabia in addition you will be supporting all registration requests by coordinating the administrative part through the channels.
Key Responsibilities:-
Maintain existing internal databases or develop new, such as the Regulatory Tracker, and develop an efficient documentation and communication system.
Supporting the importation activities by gathering, evaluating, organizing and managing documentation required for the approvals from local authorities’ systems including and not limited to SFDA, SABER & MOI.
Liaising and negotiating with local authorities
Ensuring that quality standards are met, and submissions meet strict deadlines
Review advertising and marketing material for appropriateness and compliance to regulatory requirements.
Support all registration and tender requests by coordinating the administrative part through applicable channels.
Maintain current knowledge of regulatory requirements imposed by health authorities in Saudi.
Notify & Coordinate required approvals with shipping/supply chain department.
Handling the weekly and monthly RA reports and statistics
Other duties will be assigned based on the business /role requirements
Preferred Requirements :-
Fresh Graduate / 0-1 Year experience . Regulatory Affairs background is a plus.
Education qualification - Bachelor degree in Medical field/Pharmacy background
Proficiency in spoken and written English
Phenomenal teammate
Attention to detail
Excellent communication and presentation skills.
Please note that the closing date of this advertisement is 24th May 2023
Click on apply if this sounds like you!
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
To learn more about BD visit: https://bd.com/careers
Primary Work Location
SAU Riyadh - Centria Office BuildingAdditional Locations
Work Shift
