Experienced Regulatory Affairs Lifecycle Submissions Professional

jj · Casablanca

Hybrid Mid 🇬🇧 English

Job description

About the role

Johnson & Johnson is seeking an experienced Regulatory Affairs professional to manage lifecycle submissions for emerging markets. The position is based in Casablanca, Morocco and operates in a hybrid work model, collaborating with regional and global teams to ensure timely regulatory filings.

Key responsibilities

Coordinate end‑to‑end lifecycle management procedures, including submissions, database updates and artwork changes.
Prepare submission‑ready dossiers and ensure high‑quality, on‑time delivery to health authorities.
Process health‑authority approvals and initiate post‑approval activities across the MAFSA region.
Propose strategies and timelines for National Procedure submissions and liaise with regional regulatory contacts.
Monitor lifecycle activities, identify risks, and drive internal process‑improvement initiatives.

Required profile

Fluency in French, English and Arabic.
Minimum 3 years of experience in pharmaceutical regulatory affairs.

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Source : ats:workday

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Published 2 weeks ago

Expires 1 month from now

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