Regulatory Affairs Officer M/F - 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 first aid, as well as medical consumables.
As the exclusive importer and distributor of world-renowned brands, we guarantee quality products approved by healthcare professionals. Our expertise allows us to effectively assist our clients in their equipment choices and medical prescriptions.
With 30 stores in major cities across Morocco, our team is at your service to advise you and provide you with the equipment tailored 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 :
As part of our development, we are recruiting a Regulatory Affairs Officer to join our team based in Rabat.
You will be a key player in ensuring compliance with regulatory requirements for medical devices and will ensure the conformity of our imported and distributed products in Morocco.
This position will offer you a stimulating opportunity to develop your expertise in a fast-growing environment, requiring rigor, regulatory monitoring, and inter-departmental coordination.
Your main tasks:
• Ensure the regulatory compliance of imported and distributed medical products, in accordance with Moroccan and international regulations (local laws, health directives, ISO standards, etc.).
• Prepare and update registration files for medical devices with the competent authorities.
• Conduct active regulatory monitoring of legislative and normative evolutions, both national and international, applicable to medical devices.
• Collaborate with international suppliers to collect necessary documents (CE certificates, technical files, clinical reports, etc.).
• Participate in drafting and updating quality documents related to regulations (procedures, instructions, product sheets, etc.).
• Support sales and marketing teams on the regulatory aspects of products: review of materials, verification of claims, etc.
• Act as the point of contact for health authorities in case of audits or specific requests.
Required profile :
• Bachelor's degree to Master's degree (Bac +3 to Bac +5), ideally in regulatory affairs, biology, biomedical sciences, or quality management.
• 1 to 3 years of experience in a similar role, in the medical device or pharmaceutical field, is highly appreciated.
• Knowledge of applicable standards for medical devices (ISO 13485, CE marking, etc.).
• Ability to read and write technical documents.
• Strong sense of organization, rigor, and autonomy.
• Very good communication and teamwork skills.
• Proficiency in office software (Word, Excel, PowerPoint).
• Professional English would be an asset (written and spoken).
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