Job Description
Position: Senior Pharmaceutical Regulatory Affairs Specialist
Company: GSK Gambia
Location: Brikama, Gambia
Experience: 5-7 years
Education: Master’s Degree in Pharmacy or Regulatory Science
Employment Type: Full-time
Industry: Healthcare & Pharmaceuticals
Department: Regulatory Affairs
Salary: 450,000 – 750,000 SSP
Vacancies: 1
Company Overview
GSK Gambia is a leading force in the healthcare sector, dedicated to improving human health by preventing and treating disease. As a global leader in the pharmaceutical industry, our mission is to combine science, technology, and talent to deliver life-changing medicines and vaccines. We operate with a deep commitment to ethics, integrity, and scientific excellence, ensuring that every product we bring to market meets the highest standards of safety and efficacy. Our presence in the West African region is growing, and we are looking for top-tier professionals to join our mission of enhancing patient outcomes across the continent. We provide a platform for innovation and professional growth, making us one of the most sought-after employers for those seeking meaningful career opportunities in Gambia.
Job Overview
We are currently seeking a highly skilled Senior Pharmaceutical Regulatory Affairs Specialist to join our expanding team in Brikama. This critical role is essential for ensuring that all our pharmaceutical products comply with local and international regulatory standards. The successful candidate will act as a primary liaison between the company and national health authorities, managing the lifecycle of product registrations and ensuring continuous compliance. This position is ideal for a professional who thrives in a complex, highly regulated environment and possesses a deep understanding of pharmaceutical law and clinical data. If you are looking for employment in Gambia within a world-class organization, this is a premier opportunity to advance your career. For more information on available roles, visit https://gambiajobsearch.com.
Key Responsibilities
- Lead the preparation and submission of dossiers for new product registrations and variations.
- Maintain and update regulatory licenses and ensure all documentation is current.
- Collaborate with the Quality Assurance and Manufacturing teams to ensure compliance with Good Manufacturing Practices (GMP).
- Monitor changes in local and international pharmaceutical regulations and assess their impact on current operations.
- Provide expert guidance to marketing and clinical teams regarding regulatory requirements for promotional materials.
- Manage relationships with the Ministry of Health and local regulatory bodies.
Required Skills
- Advanced knowledge of pharmaceutical regulatory frameworks and submission processes.
- Exceptional attention to detail and analytical thinking.
- Strong communication skills for interacting with government officials and internal stakeholders.
- Project management expertise in handling multiple regulatory timelines simultaneously.
- Proficiency in technical writing and dossier compilation.
Education
A Master’s degree in Pharmacy, Pharmaceutical Sciences, or Regulatory Affairs is mandatory. A Bachelor’s degree in a related life sciences field with significant specialized experience may be considered.
Experience
A minimum of 5 to 7 years of experience in regulatory affairs within the pharmaceutical industry is required. Proven experience in navigating the regulatory landscape in West Africa is highly advantageous.
Salary
The monthly salary for this position ranges from 450,000 SSP to 750,000 SSP, depending on experience and qualifications. This is a competitive package designed to attract the best talent in the region.
Benefits
- Comprehensive health and dental insurance.
- Performance-based annual bonuses.
- Generous paid time off and parental leave.
- Pension scheme and retirement planning support.
- Professional development and certification reimbursement.
Training
We believe in continuous learning. Successful candidates will have access to specialized training programs, including advanced regulatory updates and leadership development workshops. Explore more career opportunities in Gambia by visiting https://eritreajobsearch.com/.
Working Environment
The working environment is professional, collaborative, and highly structured. You will work in a modern office setting in Brikama, supported by a diverse team of scientists, clinicians, and logistics experts. We foster a culture of respect and scientific rigor.
Application Process
Interested candidates should submit their updated CV and a cover letter detailing their regulatory expertise. Please note that all applications are reviewed through our centralized recruitment portal. For more diverse job listings, check https://namibiajobsearch.com/job-vacancy-in-namibia/.
Equal Opportunity Statement
GSK Gambia 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.