Assistant Pharmacist

SARL MEDEC

Main responsibilities:   

• Assist the DT in ensuring that each batch of pharmaceutical product is manufactured and controlled, in accordance with applicable legislation and regulations and in compliance with the requirements set out in the registration decision.
• To ensure compliance with technical and administrative regulations established in the interest of public health, as well as good manufacturing practices. Within the scope of his duties, he is specifically responsible for:
• To organize and monitor all pharmaceutical operations of the establishment, including manufacturing, pharmacovigilance, monitoring and recall of batches of pharmaceutical products and medical devices concerned, as well as related storage operations.
• Ensure that transport conditions guarantee the proper preservation, integrity and safety of pharmaceutical products or related inputs.
• Take all measures to ensure that the conditions of transport, storage and preservation of medical samples cannot compromise the safety, efficacy and quality of the samples
• To declare, on a weekly basis, to the relevant departments of the Ministry of Pharmaceutical Industry the stock levels of pharmaceutical products
• Report expired products, incinerated products, and planned production schedules to the relevant departments of the ministry responsible for the pharmaceutical industry.
• Prepare the provisional import schedule for raw materials and packaging materials
• Participate in the development of the research and development program
• Ensure that a pharmaceutical quality management system is implemented and respected
• Ensure that self-inspections are carried out at regular intervals, following a pre-established program, and that the necessary corrective and preventive measures are implemented.
• Preparation of packaging materials in accordance with regulations.
• Prepare registration files for new products.
• Collect, from the R&D, testing and trials, and production departments, the various technical documentation in order to compile the registration files.

Secondary responsibilities:

• Monitoring of the various operations carried out by the technical department
• Preparation of various documents originating from the Technical Department
• Drafting and revising the procedures of the Technical Directorate

Competency criteria:

• Pharmacy degree
• Having knowledge of Good Manufacturing Practices
• Proficiency in computer skills, proficiency in the OFFICE suite (Word, Excel, PowerPoint)
• Strong organizational skills, rigor and methodology, sense of responsibility, and management qualities
• Available immediately