Senior Pharmaceutical Regulatory Affairs Specialist Job Vacancy in Blida, Algeria – Pharmaceuticals

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Specialist

Company: Sanofi Algeria

Location: Blida, Algeria

Experience: 5-7 years

Education: Master’s Degree in Pharmacy or Pharmaceutical Sciences

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Regulatory Affairs

Salary: 450,000 – 650,000 SSP

Vacancies: 1

Company Overview

Sanofi is a global leader in healthcare, dedicated to transforming science into life-changing medicines for people around the world. As a major player in the pharmaceutical sector, our presence in Algeria is vital to ensuring that high-quality healthcare solutions reach the population efficiently. We focus on innovation, patient-centricity, and rigorous scientific standards to combat various diseases. By joining our team, you become part of a global mission to improve human health through cutting-edge biotechnology and advanced chemical synthesis. We are currently expanding our operations in the Blida region to better serve the local market and provide more robust career opportunities in Algeria for highly skilled professionals.

Job Overview

We are seeking a highly meticulous Senior Pharmaceutical Regulatory Affairs Specialist to join our growing team in Blida. This role is critical in ensuring that all our pharmaceutical products comply with the stringent regulations set by the Algerian Ministry of Health and international standards. You will act as the primary liaison between the company and regulatory authorities, managing the submission of dossiers for new product registrations, variations, and renewals. This position requires a deep understanding of local and international pharmaceutical laws to ensure seamless market access for our innovative therapies. If you are looking for meaningful employment in Algeria within a high-stakes, science-driven environment, this is an exceptional opportunity. You can explore more about our mission at https://algeriajobsearch.com.

Key Responsibilities

• Manage the end-to-end lifecycle of product registrations and regulatory submissions.
• Ensure all marketing authorization applications are technically sound and compliant with local laws.
• Collaborate with Quality Assurance and Production teams to ensure manufacturing processes meet regulatory standards.
• Monitor changes in the regulatory landscape in Algeria and provide strategic advice to management.
• Prepare and review technical documentation, including dossiers for new drug applications.
• Coordinate with external regulatory agencies to resolve queries regarding product licensing.

Required Skills

• Expert knowledge of Algerian pharmaceutical regulations and international ICH guidelines.
• Strong analytical skills for reviewing complex technical and scientific documentation.
• Excellent communication skills for interacting with government officials and internal stakeholders.
• High attention to detail to ensure zero errors in regulatory filings.
• Project management skills to handle multiple product lifecycles simultaneously.

Education

A Master’s degree or Doctorate in Pharmacy, Pharmaceutical Sciences, or a closely related Life Sciences field is mandatory for this position.

Experience

A minimum of 5 to 7 years of direct experience in regulatory affairs within the pharmaceutical industry is required. Proven experience in dealing with the Algerian Ministry of Health is highly preferred.

Salary

The monthly salary for this position ranges from 450,000 SSP to 650,000 SSP, depending on experience and qualifications.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health and life insurance coverage.
• Access to international training and development programs.
• Modern and safe working environment.
• Opportunities for global mobility within the Sanofi network.

For more international career paths, visit https://tanzaniajobsearch.com/.

Training

• Advanced Regulatory Compliance workshops.
• Internal leadership and management training.
• Specialized technical training on new pharmaceutical technologies.

Working Environment

The working environment is professional, collaborative, and highly structured. You will work in a modern office setting in Blida, collaborating with diverse teams including R&D, Quality, and Supply Chain. We foster a culture of scientific excellence and continuous learning.

Application Process

Interested candidates should submit their updated CV and a cover letter detailing their regulatory expertise. Please ensure all certifications are ready for verification. For more job vacancies in the region, check https://kenyajobsearch.com/job-vacancy-in-kenya/.

Equal Opportunity Statement

Sanofi is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, religion, gender, or background. We are hiring in Algeria to build a diverse workforce that reflects the communities we serve.