Analyst RPSR

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Product Submissions and Registration

Job Category:
Professional

All Job Posting Locations:
Cairo, Egypt

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Regulatory Affairs Professional - KSA & Gulf.

This hybrid work position will be located in Cairo, Egypt.

Essential Job Duties and Responsibilities:


* Execute regulatory plans and manage timelines to achieve the stated goals.


* Coordinate the preparation, review, submission, Tracking and follow-up of regulatory files (including but not limited to: New MA dossiers, renewals, variations, response to questions) that are properly formatted and in compliance with local regulations.

Prepare local/administrative sections where no local regulatory responsible is designated according to country specific requirements.


* Act as liaison and main contact between LOCs and international groups: I.

Receive, assess completeness/relevance, track and archive core dossiers received from international groups.

II.

Forward all relevant information/data from and in accordance with international group LOCs.

III.

Keep international groups informed of regulatory statuses in LOCs and forward to them requests and relevant information from LOCs.


* Maintain archiving and appropriate databases and systems: I.

Ensure electronic and paper tracking of regulatory activities and Marketing authorizations lifecycle.

II.

Ensure archiving of regulatory dossiers.

III.

Populate and update appropriate J&J databases as per J&J processes.

IV.

Update, maintain and use regulatory databases, tracking tables and information systems.

Daily business & product supply Support:


* Provide guidance to p...