Regulatory Affairs Officer - Medical Devices - Rabat

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 an exclusive importer and distributor of world-renowned brands, we guarantee quality products validated by healthcare professionals. Our expertise allows us to effectively support our clients in their equipment choices and medical prescriptions.

With 30 stores in the major cities of Morocco, our team is at your service to advise you and provide you with the equipment adapted to your needs. Looking resolutely towards 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 company in the Medical Equipment sector, where your expertise will be at the heart of our development. We are looking for a Regulatory Affairs Officer - Medical Devices for our site in Rabat. If you aspire to contribute to bringing innovative products to market and ensure their compliance, this opportunity is for you.

Actively contribute to the company's regulatory strategy, ensuring the compliance of medical device products with national and international standards. The main objective is to facilitate market access while maintaining the highest standards of quality and safety.

Your main responsibilities will focus on several key areas:

• Preparation and submission of medical device registration files to the competent authorities.
• Proactive regulatory monitoring to anticipate legislative and normative changes.
• Regulatory support for development, production, and marketing teams.
• Management of audits and inspections by authorities.
• Evaluation and management of risks related to product compliance.
• Writing and updating technical and regulatory documentation.
• Advice and support on medical device regulation issues.

Required profile :

To excel in this role, a Bachelor's degree (Bac+3) is required.

Professional experience of 3 to 5 years in the regulatory field of medical devices is essential to fully grasp the challenges of the position.

This position requires a combination of strong technical and behavioral skills:

• Excellent knowledge of regulations applicable to medical devices (national and international).
• Proven analytical and synthesis skills.
• Rigor, organization, and attention to detail.
• Proficiency in computer tools and regulatory databases.
• Ability to communicate effectively with various stakeholders.
• Autonomy and proactivity in file management.
• Good command of French and English, both written and spoken.

If you see yourself in this description and are motivated by the idea of taking on new challenges, do not hesitate to apply!

Head office address :

Desired personality traits :

Respect of the rules Tenacity Need for action Team work Involvement at work Humbleness Organization