Regulatory Affairs Manager Job Vacancy in Gunjur, Gambia – Pharmaceuticals

Job Description

Position: Regulatory Affairs Manager

Company: GlaxoSmithKline (GSK)

Location: Gunjur, Gambia

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: 150,000 – 250,000 SSP per month

Vacancies:1

Company Overview

GlaxoSmithKline (GSK) is a global healthcare company dedicated to improving the health and well‑being of people around the world. With a strong presence across Africa, GSK operates manufacturing, research, and commercial facilities that adhere to the highest standards of quality and compliance. In Gambia, GSK collaborates with local health authorities, distributors, and research institutions to ensure that essential medicines and vaccines reach underserved communities. The company’s commitment to innovation, sustainability, and community development makes it a leading employer for professionals seeking meaningful impact in the pharmaceutical sector. As part of its expansion strategy, GSK is establishing a Regulatory Affairs hub in Gunjur to support product registration, compliance monitoring, and market access across West Africa.

GSK’s reputation for excellence, combined with its focus on employee growth, creates a dynamic environment where talent thrives. The organization consistently ranks among the top employers for its inclusive culture, competitive compensation, and robust training programs. Candidates joining GSK in Gambia will be part of a diverse team that values scientific rigor, ethical conduct, and collaborative problem‑solving.

Job Overview

The Regulatory Affairs Manager will lead the regulatory strategy for GSK’s product portfolio in Gambia and neighboring markets. This role involves preparing and submitting dossiers to the National Medicines Regulatory Authority (NMRA), ensuring compliance with local and international guidelines, and providing strategic advice to cross‑functional teams. The manager will act as the primary liaison between GSK and regulatory bodies, facilitating timely approvals and maintaining product integrity throughout the product lifecycle.

For more information about career opportunities in Gambia, visit our main portal: https://gambiajobsearch.com

Explore similar roles across East Africa at https://tanzaniajobsearch.com/job-vacancy-tanzania/

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Key Responsibilities

• Develop and execute regulatory strategies for new product registrations, variations, and renewals in Gambia.
• Prepare, review, and submit comprehensive dossiers, including CTD modules, to the NMRA and other relevant authorities.
• Maintain up‑to‑date knowledge of local and international regulations, guidelines, and best practices.
• Coordinate with R&D, Quality Assurance, Clinical, and Commercial teams to ensure alignment on regulatory requirements.
• Lead interactions with regulatory agencies, responding to queries, and negotiating timelines.
• Monitor post‑approval compliance, adverse event reporting, and product labeling updates.
• Provide regulatory risk assessments and advise senior management on market entry decisions.
• Train internal stakeholders on regulatory processes, documentation standards, and compliance expectations.

Required Skills

• In‑depth understanding of Gambia’s pharmaceutical regulations and ICH guidelines.
• Proven experience preparing successful regulatory submissions for medicines or vaccines.
• Excellent written and verbal communication skills in English; French is an advantage.
• Strong analytical and problem‑solving abilities with attention to detail.
• Ability to manage multiple projects simultaneously and meet tight deadlines.
• Leadership skills to mentor junior staff and drive cross‑functional collaboration.
• Proficiency with regulatory software tools and document management systems.

Education

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

Experience

Minimum of five years of hands‑on regulatory affairs experience within a multinational pharmaceutical company or a reputable contract research organization. Experience with product registration in African markets, especially West Africa, will be considered a strong asset.

Salary

The position offers a competitive salary range of 150,000 to 250,000 SSP per month, commensurate with experience and qualifications. Performance‑based bonuses and annual cost‑of‑living adjustments are part of the total compensation package.

Benefits

• Comprehensive health insurance covering medical, dental, and vision.
• Retirement savings plan with employer contributions.
• Generous paid time off, including vacation, sick leave, and public holidays.
• Professional development allowance for certifications, conferences, and courses.
• Employee assistance program and wellness initiatives.

Training

• Onboarding program covering GSK’s global regulatory framework and local compliance requirements.
• Access to GSK’s internal learning platform for continuous skill enhancement.
• Mentorship from senior regulatory leaders across the region.
• Opportunities to attend international regulatory workshops and industry conferences.

Working Environment

GSK’s Gunjur office provides a modern, collaborative workspace equipped with state‑of‑the‑art technology and comfortable meeting areas. The company promotes a culture of safety, inclusivity, and work‑life balance, encouraging flexible working arrangements where feasible. Employees benefit from a supportive leadership team that values transparency, ethical conduct, and employee well‑being.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their regulatory experience through the GSK careers portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be invited for a virtual interview followed by an on‑site assessment at the Gunjur office.

Equal Opportunity Statement

GlaxoSmithKline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic. All qualified applicants will receive consideration for employment without discrimination.