Veterinary Technical Director

Baladna Dairy Farm Project – Adrar, Algeria

The Baladna Dairy Farm Project in Adrar, Algeria, is being implemented within the framework of a strategic partnership between Baladna Q.P.S.C. and the Government of Algeria.

The project is located in Timokten, approximately 100 kilometers from the city of Adrar and around 1,435 kilometers southwest of Algiers.

Its operations will be carried out across three distinct sites in southern Algeria, primarily within the province of Adrar. Covering a total area of about 117,000 hectares, the Baladna Algeria Project encompasses three major pillars:

• The production of cereals and fodder

• Cattle farming for the production of milk and meat

• A state-of-the-art milk powder processing facility

The project will be executed in several phases, ultimately reaching a production capacity of 198,000 tons of milk powder.

1- Job Purpose: The Veterinary Technical Director is responsible for overseeing the technical and regulatory aspects of veterinary medicinal products, ensuring compliance with applicable Algerian regulations, and coordinating activities related to regulatory affairs, pharmacovigilance, technical dossier assessment, and continuing professional development for the company’s veterinary teams.

The position requires strong veterinary expertise, extensive knowledge of the Algerian regulatory framework, and proven experience in managing regulatory procedures and dossiers with the Veterinary Services Directorate (Direction des Services Vétérinaires – DSV).

2- Key Responsibilities and Duties:

2.1. Regulatory Affairs and Compliance

• Monitor and analyze Algerian legislation and regulatory requirements applicable to veterinary medicinal products and related activities.

• Ensure the timely identification of regulatory changes and assess their potential impact on the company’s operations.

• Prepare, review, and follow up on regulatory dossiers submitted to the competent authorities, particularly the Veterinary Services Directorate (DSV).

• Coordinate the preparation and submission of required administrative, scientific, and technical documentation.

• Maintain professional communication with the relevant regulatory authorities regarding matters falling within the scope of the position.

• Provide technical guidance and recommendations to internal stakeholders to support regulatory compliance.

• Ensure the proper maintenance and updating of regulatory records and documentation.

2.2. Veterinary Pharmacovigilance

• Coordinate the monitoring of pharmacovigilance activities relating to veterinary medicinal products used within the company’s operations.

• Collect, review, analyze, and document information relating to suspected adverse reactions and incidents associated with veterinary medicinal products.

• Assess potential risks associated with the use of veterinary medicinal products and recommend appropriate technical measures.

• Prepare, review, and follow up on pharmacovigilance reports in accordance with applicable regulatory requirements.

• Ensure the appropriate documentation and traceability of pharmacovigilance information.

• Coordinate with relevant internal stakeholders and external parties, as necessary, to support pharmacovigilance compliance.

2.3. Technical Assessment of Veterinary Medicinal Product Registration Dossiers

• Prepare technical assessment and expert reports relating to the safety and efficacy of veterinary medicinal products submitted for registration.

• Review and critically assess scientific, technical, and regulatory documentation included in registration dossiers.

• Evaluate the consistency, completeness, and relevance of the available data relating to product safety and efficacy.

• Identify gaps or deficiencies in submitted documentation and recommend the appropriate corrective actions.

• Contribute to the preparation, review, and updating of registration dossiers and supporting technical documentation.

• Follow up on regulatory requirements and requests for additional information issued by the competent authorities.

• Provide technical recommendations to support the registration and regulatory monitoring of veterinary medicinal products.

2.4. Continuing Professional Development and Veterinary Training

• Identify the training needs of the company’s veterinary professionals in relation to regulatory requirements, pharmacovigilance, and veterinary technical practices.

• Develop and propose an annual continuing professional development plan for veterinary teams.

• Design and deliver training sessions covering veterinary medicinal product regulations, pharmacovigilance, the safe use of medicinal products, and relevant professional practices.

• Support the continuous updating of veterinarians’ scientific, technical, and regulatory knowledge.

• Prepare appropriate training materials, technical guidance documents, and educational resources.

• Monitor training attendance, assess training effectiveness, and maintain records of completed training activities.

• Contribute to ensuring that veterinary training activities are aligned with applicable professional and regulatory requirements.

3. Key Professional Interfaces

The Veterinary Technical Director shall work closely with:

• General Management and relevant operational departments.

• Veterinary teams and livestock operations managers.

• Regulatory affairs, quality, and compliance teams, where applicable.

• The Veterinary Services Directorate (DSV) and other relevant regulatory authorities.

• External technical experts and other stakeholders involved in veterinary medicinal product registration, pharmacovigilance, and regulatory compliance.

4. Required Qualifications and Experience

4.1. Mandatory Requirements

• Education: A Doctor of Veterinary Medicine degree is mandatory.

• Professional Experience: 8 to 10 years of relevant professional experience in the veterinary field.

• Regulatory Experience: Proven experience in preparing, submitting, processing, and following up on regulatory dossiers with the Veterinary Services Directorate (DSV) in Algeria.

• Regulatory Knowledge: Strong knowledge of Algerian legislation and regulatory requirements applicable to veterinary medicinal products.

• Technical Expertise: Demonstrated experience in veterinary pharmaceutical regulations, product registration procedures, and the preparation or assessment of technical and scientific documentation.

4.2. Preferred Qualifications and Experience

• Practical experience in veterinary pharmacovigilance and regulatory reporting.

• Experience in assessing scientific data relating to the safety and efficacy of veterinary medicinal products.

• Experience in preparing technical reports and responding to regulatory requests for additional information.

• Experience in designing and delivering technical training programs for veterinary professionals.

• Additional training or specialization in veterinary pharmaceutical regulations, pharmacovigilance, or regulatory affairs is an advantage.

5. Required Competencies

Technical Competencies

• Strong understanding of the Algerian regulatory framework governing veterinary medicinal products.

• Proven ability to manage regulatory dossiers and procedures with the DSV.

• Strong analytical skills in reviewing scientific and technical documentation.

• Proficiency in preparing technical assessment reports and regulatory submissions.

• Knowledge of pharmacovigilance principles and reporting requirements.

• Ability to develop and deliver technical training programs.

Behavioral Competencies

• High level of accuracy, rigor, and professional integrity.

• Strong analytical and problem-solving abilities.

• Excellent written communication and reporting skills.

• Effective planning, organization, and time management.

• Ability to work independently and collaboratively with multidisciplinary teams.

• Professional discretion and respect for confidentiality.