Associate RA Professional EMEA EM - Near East

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:
Beirut, Lebanon

Job Description:

The Near East Regulatory Affairs team is seeking a talented Associate Regulatory Affairs professional to support our mission of accelerating patient access to innovative healthcare solutions.

The role offers broad exposure to regulatory strategy, portfolio management, external stakeholder engagement, and cross-functional collaboration across multiple markets.

You will join a high-performing team recognized for its commitment to excellence, innovation, and patient-focused impact.

Essential Job Duties and Responsibilities

Act as Associate Regulatory Affairs Professional for NE Countries within specific therapeutic areas: Hematology-PAH-CNS

Extended - CVT member


* Provide strategic and valuable RA input into CVT and Value excellence teams, whenever needed.


* Understand Business model and strategy drivers.


* Cooperation and partnership horizontally with commercial, MAF and other functions (Govern.

Affairs, BQ, Human Resources, Logistics...)


* Act as regulatory representative on project teams and provide advice on specific projects contributing to the development of project plans and target product profiles; whenever needed

TA Specialist



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


* b.

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; MA transfer and distributor changes...) 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:
+ Receive, assess completeness/relevance, track and archive core dossiers received from international groups.
+ Forward all relevant information/data from and in accordance with internat...