Description
Job Description Summary:
Be part of something bigger!
BD 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. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.
As a Regulatory Affairs Specialist, you will be responsible for launching of Medical Device & In-Vitro Diagnostic Products in the Egyptian Market in addition to facilitating the importation of shipments and ensuring the absence of any regulatory issue in alignment with company standards and country regulations.
**Other Key Responsibilities:
- Submission of registration for key launches for medical devices (MDs) and in-vitro diagnostics (IVDs) as well as following up closely until license issuance
- Managing regulatory lifecycle product management through re-registration, renewal, and variation Submission on time as required.
- Clearance support to distributors by providing all required documentation for importation.
- Updating RIM, tracking sheets, and monthly reports to reflect work in progress in an organized fashion.
- Responding to Notifications of Change (NOCs) & Impact Assessments (IAs) with clear responses on time.
- Tender support to commercial teams & distributors.
- Providing regular support, feedback, status updates and coordination related to Egypt for all Business Units to related internal and external stakeholders.
- Working closely with regulatory affairs internal affiliates to capture the existing and upcoming regulatory expectations and take appropriate actions.
- Managing storage facility and tracking of samples as per the local guidelines
- Having a solid communication with the Egyptian Drug Authority regulators while having a deep understanding of the local regulations, guidelines, and processes.
- Developing a close partnership with local business and distributors for coordinating regulatory activities with their teams
- Close & efficient follow up with EDA reviewers.
**About You:
- Bachelor’s (B.Sc.) Degree in Medical Field, preferably in Pharmaceutical Sciences
- 2-3 years in the Regulatory Affairs, preferably in the Medical Devices Sector
- Proficiency in spoken and written English and Arabic. French is a plus.
- Attention to details and very good organizational skills.
- High sense of urgency and ownership.
- Excellent communication and presentation skills.
- Successful history in prioritizing multiple projects, scheduling activities as well as managing tight deadlines
- Great teammate, agile, and demonstrating resilient attitude
Why join us?
A career at BD means that you are part of a team that values your opinions and contributions and that empowers you to bring your authentic self to work. Here you can fulfill your life’s purpose through the work that you do every day.
You will learn and work alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. Our Total Rewards program — which includes competitive pay, benefits, continuous learning, recognition, career growth, and life balance components — is designed to support the varying needs of our diverse and global associates.
Becton, Dickinson and Company is an Equal Opportunity 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, or any other protected status.
Primary Work Location: EGY EGYPT - Field Only
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