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

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Manager

Company: Sanofi Algeria

Location: Blida, Algeria

Experience: 8-10 years

Education: Master’s Degree in Pharmacy or Life 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 mission is to pursue the breakthroughs in science to improve people’s lives. In Algeria, we are committed to providing high-quality healthcare solutions and ensuring that innovative treatments reach the patients who need them most. We foster a culture of innovation, integrity, and excellence, making us one of the most sought-after employers for professionals seeking meaningful career opportunities in Algeria. Our presence in the region is marked by a commitment to local health standards and global scientific excellence.

Job Overview

We are seeking a highly skilled and strategic Senior Pharmaceutical Regulatory Affairs Manager to lead our regulatory compliance efforts in the Algerian market. This critical role involves navigating complex legal frameworks to ensure all our products meet the stringent requirements of local and international health authorities. The successful candidate will act as the primary liaison between the company and regulatory bodies, ensuring that all product registrations, variations, and compliance documentation are handled with precision. This is a high-impact role that directly influences our ability to bring life-saving medications to the Algerian population. For those looking for professional growth, this position offers unparalleled career opportunities in Algeria within a world-class scientific environment. You can explore more professional paths at https://algeriajobsearch.com.

Key Responsibilities

• Lead the preparation and submission of all regulatory dossiers for new product registrations and lifecycle management.
• Ensure continuous compliance with Algerian Ministry of Health regulations and international standards.
• Manage relationships with local health authorities and represent the company during inspections.
• Collaborate with global R&D and supply chain teams to align local requirements with international manufacturing standards.
• Monitor changes in the regulatory landscape to proactively adjust company strategies and documentation.
• Oversee the labeling and packaging compliance for all products entering the Algerian market.

Required Skills

• Expert knowledge of local and international pharmaceutical regulatory guidelines.
• Strong strategic thinking and ability to manage complex, multi-stakeholder projects.
• Exceptional communication skills in both Arabic and French.
• High attention to detail regarding technical documentation and legal compliance.
• Proven ability to lead and mentor a team of regulatory specialists.

Education

A Master’s degree or Doctorate in Pharmacy, Pharmaceutical Sciences, or a closely related Life Sciences field is mandatory. Advanced certifications in Regulatory Affairs are highly preferred.

Experience

A minimum of 8 to 10 years of progressive experience in pharmaceutical regulatory affairs is required, with at least 3 years in a leadership or managerial capacity. Previous experience working within a multinational pharmaceutical corporation is essential for success in this role.

Salary

The offered salary for this position is between 450,000 and 650,000 SSP per month, depending on the candidate’s expertise and proven track record in the industry.

Benefits

• Competitive compensation package aligned with international standards.
• Comprehensive health and wellness insurance for employees and dependents.
• Performance-based annual bonuses.
• Access to global training and development programs.
• Opportunities for international mobility within the Sanofi network.

Training

Successful candidates will undergo intensive onboarding regarding Sanofi’s global compliance protocols. We also provide continuous professional development through specialized workshops and access to international regulatory seminars. For more information on global job trends, visit https://tanzaniajobsearch.com/.

Working Environment

The working environment is professional, collaborative, and highly structured. You will work in a modern office setting in Blida, interacting with diverse teams across different time zones. While the role is primarily office-based, occasional travel to regulatory agencies or manufacturing sites may be required. We prioritize a work-life balance and provide the tools necessary for remote collaboration when required.

Application Process

Interested candidates should submit their updated CV and a cover letter detailing their regulatory expertise through our official portal. We are looking for individuals who demonstrate a passion for healthcare and a commitment to excellence. Please note that only shortlisted candidates will be contacted for interviews. For more diverse employment options, 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. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, or disability status.