Experienced Regulatory Affairs Lifecycle Submissions Professional
jj · Casablanca
Description du poste
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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jj
Casablanca
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