رئيس قسم الشؤون التنظيمية

Company Description Pharmacon Pharmaceuticals is a Germany-Egyptian pharmaceutical company focused on introducing licensed, high-quality products to the Egyptian market. Established in 2004, the company aims to improve patient health by providing alternative medical solutions and addressing unmet needs across diverse therapeutic areas. Pharmacon’s portfolio is sourced from high-standard European partners, prioritizing safety, efficacy, and competitive pricing. The organization is committed to enhancing quality of life through accessible, affordable treatments and to recruiting and developing high-caliber employees who share its values. Pharmacon’s long-term vision is to expand its presence across multiple therapeutic areas and become one of the leading pharmaceutical companies in Egypt.

Role Description Execute the regulatory plans ensuring close follow up with the licensors and timely reporting.

• Preparation and submission of registration dossiers, variations, renewals, and relevant activities, ensuring timely execution.

• Ensure compliance of product labeling, packaging, with local regulations and internal policies.

• Monitors timelines for key submissions for all types of products; pharmaceuticals, biological, medical devices, food supplement and cosmetics.

• execute of registration of local pharmaceuticals, food supplements, cosmetics at EDA and NFSA.

• prepare, submit and follow up the importation license, importation plans & approvals, lot release documentation, custom medical release, inspection release for all type of products.

• prepare, submit and follow up the importation license, plans, lot release documentation, custom medical release, inspection release for all type of products.

• Contribute to the development, improvement and expansion of the company`s portfolio and related project management.

Qualifications

• Bachelor’s degree in Pharmacy.

• Minimum of 2 years of experience in a similar position.

• Fluency in English, both written and verbal are a must.

• Good understanding of regulations and related guidelines.

• Familiarity with different regulatory dossiers (CTD, eCTD) is a must.

• Strong personality, organizational skills and ability to plan and manage own work agenda independently.

• Ability to collaborate effectively.

• Strong interpersonal communication and organizational skills.

• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

• Ability to collaborate effectively.