At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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:

Casablanca, Morocco

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 an Experienced RA Professional Lifecycle Submissions to be in Casablanca, Morocco.

Cross-Regional Operations & Strategic Support (C-ROSS) is a regional capability driven Regulatory Affairs organization working in close collaboration with Local Operation Companies (LOC), regional and global teams.

The responsibility of C-ROSS Lifecycle Submissions for Maghreb (Tunisia, Morocco and Algeria) and FFrench-speakingAfrica is to coordinate lifecycle management procedures in-scope from end to end, ensuring timely submission, implementation of the change in the applicable databases and, if applicable, artwork.

Main Duties And Responsibilities

• Perform lifecycle management activities per established processes and country-specific requirements.

• Propose strategy and timeline for National Procedure (NP) to the LOC.

• Prepare submission-ready documents/dossier(s) and ensure timely submission of high-quality (response) dossier.

• Process Health Authority (HA) approvals to initiate post-approval activities promptly.

• Ensure timely update of databases throughout lifecycle management.

• Involve ERMC colleagues and external stakeholders at appropriate process steps.

• Proactively monitor from end-to-end perspective regarding timely completion of lifecycle management activities and escalate issues.

• Actively engage in internal process improvement initiatives and contributing to the implementation of new regional/local requirements, tools, and systems.

• Act as Subject Matter Expert (SME)/ Single Point of Contact (SPOC) for assigned topics as ERMC (sub) team representative.

• Involvement in other tasks and/or projects based on business needs as assigned by line manager.

Qualifications

• Arabic and English knowledge is required, French is an asset.

• Pharmacist bachelor’s degree

• Minimum of 3 years of Regulatory Affairs experience within Emerging Markets.

• Works under general supervision to contribute to projects and tasks.

• Individual contributor who performs more complex assignments and contributes to projects and processes within their area of responsibility.

• Applies general knowledge and understanding of principles and practices to address problems.

Required Skills

Preferred Skills: