Regulatory Affairs Manager Job Vacancy in Louga, Senegal – Pharmaceuticals

Job Description

Position: Regulatory Affairs Manager

Company: Sanofi

Location: Louga, Senegal

Experience: 5+ years in regulatory affairs within pharmaceutical industry

Education: Bachelor’s degree in Pharmacy, Life Sciences, or related field; Master’s preferred

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Regulatory Affairs

Salary: 2,500,000 – 3,500,000 SSP per month

Vacancies:1

Company Overview

Sanofi is a global healthcare leader dedicated to improving lives through innovative medicines, vaccines, and consumer health solutions. With a strong commitment to the African continent, Sanofi operates in Senegal, delivering essential medicines and supporting local health initiatives. The company’s presence in Senegal reflects its strategic focus on emerging markets, fostering partnerships with local authorities, research institutions, and healthcare providers. As part of its mission to enhance public health, Sanofi contributes to capacity building, disease prevention, and access to quality treatments, making it a respected employer for professionals seeking meaningful impact in the pharmaceutical sector.

Located in the vibrant city of Louga, Sanofi’s regional hub serves as a critical node for regulatory compliance, product registration, and market access across West Africa. The organization values diversity, innovation, and ethical standards, offering a collaborative environment where talent can thrive while contributing to the broader goal of improving health outcomes in Senegal and beyond. This role aligns with Sanofi’s vision of delivering life‑changing solutions and offers a unique opportunity to shape regulatory strategies in a dynamic market.

Job Overview

The Regulatory Affairs Manager will lead Sanofi’s regulatory strategy for product submissions, approvals, and compliance within Senegal. Reporting to the Head of Regulatory Affairs, the incumbent will coordinate with cross‑functional teams, government agencies, and external partners to ensure that all pharmaceutical products meet local and international regulatory standards. This position plays a pivotal role in accelerating time‑to‑market for new medicines while safeguarding patient safety and adhering to ethical practices. For more information about Sanofi’s career opportunities, visit https://senegaljobsearch.com/.

As a cornerstone of Sanofi’s operations in Louga, the Regulatory Affairs Manager will be instrumental in navigating the evolving regulatory landscape, influencing policy discussions, and fostering strong relationships with the National Agency for the Pharmaceutical Sector (ANSP). The role offers exposure to a broad portfolio of products, from vaccines to specialty medicines, and requires a proactive approach to regulatory intelligence and risk management.

Key Responsibilities

• Develop and execute regulatory strategies for new product registrations, variations, and renewals in Senegal.
• Prepare, review, and submit dossiers to the ANSP, ensuring compliance with local guidelines and international standards such as ICH and WHO.
• Maintain up‑to‑date regulatory intelligence, monitor legislative changes, and advise internal stakeholders on impact and required actions.
• Collaborate with R&D, Quality Assurance, Clinical, and Commercial teams to align product development with regulatory requirements.
• Lead interactions with health authorities, including meetings, inspections, and negotiations, to facilitate timely approvals.
• Oversee post‑marketing surveillance activities, adverse event reporting, and product lifecycle management.
• Develop and maintain a comprehensive regulatory database and ensure accurate documentation of all submissions.
• Provide training and mentorship to junior regulatory staff and cross‑functional colleagues on regulatory best practices.
• Support business development initiatives by assessing regulatory feasibility of potential acquisitions or partnerships.

Required Skills

• In‑depth knowledge of Senegalese pharmaceutical regulations and international guidelines (ICH, WHO, EU).
• Strong analytical and problem‑solving abilities with attention to detail.
• Excellent written and verbal communication skills in French and English.
• Proven project management skills, capable of handling multiple dossiers simultaneously.
• Ability to build and maintain effective relationships with regulatory authorities and internal stakeholders.
• Proficiency in regulatory submission software and Microsoft Office suite.
• Leadership qualities with experience in coaching and developing teams.

Education

A Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related life‑science discipline is required. A Master’s degree or advanced regulatory certification (e.g., RAC, RAPS) is highly desirable and demonstrates a commitment to professional development in regulatory affairs.

Experience

Minimum of five years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with a focus on African markets. Experience handling full lifecycle submissions, interacting with health authorities, and managing post‑marketing obligations is essential.

Salary

The competitive salary range for this position is 2,500,000 – 3,500,000 SSP per month, commensurate with experience and qualifications. Sanofi also offers performance‑based bonuses and a comprehensive benefits package.

Benefits

• Health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Paid annual leave and public holidays in accordance with Senegalese labor law.
• Professional development allowance for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• Onboarding program covering Sanofi’s global regulatory policies and local compliance requirements.
• Continuous learning opportunities through internal e‑learning platforms and external regulatory workshops.
• Mentorship from senior regulatory leaders across the Sanofi network.

Working Environment

Sanofi’s Louga office provides a modern, collaborative workspace equipped with the latest technology to support regulatory activities. The culture emphasizes teamwork, transparency, and a shared commitment to improving health outcomes. Employees enjoy a balanced work‑life environment, with flexible working arrangements where applicable, and a supportive leadership team that encourages innovation and professional growth.

Application Process

Interested candidates should submit their application through the Sanofi careers portal linked on the Senegal Job Search website. The application must include an updated CV, a cover letter highlighting relevant regulatory experience, and copies of relevant certifications. Shortlisted applicants will be invited to a virtual interview followed by an on‑site assessment at the Louga office.

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 gender, race, religion, age, disability, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.