Regulatory Affairs and Registration Officer - Rabat
Company sector : Medical Equipment / Drugstore
COMPANY :
For over 30 years, LOCAMED has been the leader in the distribution of medical equipment in Morocco. We offer a wide range of products covering orthopedics, mobility aids, home care, hospital equipment, physiotherapy, sports and emergency care, as well as medical supplies.
Exclusive importer and distributor of world-renowned brands, we guarantee quality products approved by health professionals. Our expertise allows us to effectively support our clients in their equipment choices and medical prescriptions.
With 30 stores in major Moroccan cities, our team is at your service to advise you and provide you with the equipment adapted to your needs. Resolutely focused on the future, we are committed to improving healthcare and contributing to the well-being of the population.
Company culture :
Locamed embraces a largely cooperation-driven culture, placing people, trust and teamwork at the heart of its organization. The company favors a close management style focused on support, empowerment and strong professional relationships. This collaborative foundation is complemented by a notable innovation component, encouraging initiative, creativity and adaptability. Competitive and organizational aspects remain secondary, helping structure operations and support performance objectives.
Job :
Join a dynamic player in the medical equipment sector in Rabat. This opportunity as a Regulatory Affairs and Registration Officer offers a central role in ensuring the market launch and ongoing compliance of medical devices essential for patient health.
The role aims to manage the entire product registration process with the competent authorities to secure commercial activities. It involves ensuring that each piece of equipment strictly complies with current standards, while facilitating the administrative exchanges necessary for the company's catalog development.
Daily responsibilities require accuracy and foresight for optimal file management:
- Prepare and submit registration application files to health authorities.
- Maintain constant regulatory watch to adapt procedures to legislative changes.
- Coordinate communications with health authorities to respond to their requests for additional information.
- Manage technical documentation related to medical devices to ensure impeccable traceability.
- Provide expert support to other departments regarding compliance requirements.
Required profile :
The ideal candidate holds a Bachelor's degree (Bac +3), ideally with further specialization in the medical or paramedical field.
Confirmed professional experience of 3 to 5 years is essential to master the specifics of regulatory files in the medical industry.
Excellent understanding of regulatory affairs issues is expected. Success in this role requires:
- Precise writing skills for compiling administrative files.
- Exemplary rigor in managing technical and scientific documentation.
- Interpersonal skills to interact effectively with authorities and internal partners.
- Excellent analytical ability to anticipate sector changes.
Interested in this challenge? If your profile matches the skills presented, it is advised to submit your application now via the button "Send my CV to the recruiter".
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