Regulatory Affairs Specialist Job Vacancy in Bo, Sierra Leone – Pharmaceuticals

Job Description

Position: Regulatory Affairs Specialist

Company: GlaxoSmithKline Sierra Leone

Location: Bo, Sierra Leone

Experience: 2-4 years

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

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Regulatory Affairs

Salary: SSP 1,200,000 – 1,800,000 per annum

Vacancies:1

Company Overview

GlaxoSmithKline Sierra Leone (GSK) is a leading global healthcare company dedicated to improving the health and well-being of people worldwide. With a strong presence in Sierra Leone, GSK operates from its regional hub in Bo, delivering innovative medicines, vaccines, and consumer health products. The company is committed to sustainable development, local capacity building, and fostering partnerships that enhance public health outcomes across the nation. As part of its mission, GSK actively supports Sierra Leone Jobs initiatives, contributing to economic growth and creating meaningful career opportunities in the pharmaceutical sector.

Job Overview

The Regulatory Affairs Specialist will play a pivotal role in ensuring that all GSK products comply with local and international regulatory requirements. This position involves preparing and submitting dossiers, liaising with the Sierra Leone Ministry of Health and Sanitation, and supporting cross‑functional teams to navigate complex regulatory landscapes. The role is essential for maintaining product quality, safety, and market access, directly influencing the success of GSK’s portfolio in the region. For more information about GSK’s commitment to career development, visit our partner portal at https://sierraleonejobsearch.com.

Key Responsibilities

• Prepare, review, and submit regulatory dossiers for new product registrations and variations.
• Maintain up‑to‑date knowledge of Sierra Leonean pharmaceutical regulations and international guidelines.
• Coordinate with internal teams to gather technical documentation and ensure compliance.
• Act as the primary point of contact with regulatory authorities, facilitating inspections and audits.
• Monitor regulatory changes and advise senior management on potential impacts.
• Develop and maintain a regulatory intelligence database to support strategic decision‑making.

Required Skills

• Strong analytical and problem‑solving abilities with attention to detail.
• Excellent written and verbal communication skills in English.
• Proficiency in regulatory submission software and Microsoft Office Suite.
• Ability to work collaboratively across multidisciplinary teams.
• Project management experience with the capacity to meet tight deadlines.
• Understanding of Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP) standards.

Education

A minimum of a Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related life‑science discipline is required. Advanced certifications in regulatory affairs or a Master’s degree are considered an asset and demonstrate a commitment to professional growth.

Experience

Candidates should have 2 to 4 years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to both local and international regulatory environments. Experience with product lifecycle management and submission processes for medicines and vaccines is highly desirable.

Salary

The compensation package ranges from SSP 1,200,000 to SSP 1,800,000 per annum, commensurate with experience and qualifications. The package includes performance‑based incentives and comprehensive benefits designed to support employee well‑being.

Benefits

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

Training

• Onboarding program covering GSK’s regulatory framework and SOPs.
• Continuous learning modules on global regulatory updates.
• Mentorship opportunities with senior regulatory experts.
• Access to internal e‑learning platforms for skill enhancement.

Working Environment

GSK Sierra Leone offers a collaborative, inclusive, and dynamic workplace where innovation thrives. Employees benefit from modern office facilities in Bo, flexible working arrangements, and a culture that values diversity, integrity, and scientific excellence. The company encourages a healthy work‑life balance and supports community engagement initiatives.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their suitability for the role through our online portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. For detailed application instructions, please visit https://www.sierraleonejobsearch.com/. GSK is an equal opportunity employer and welcomes applications from all qualified individuals.

Equal Opportunity Statement

GlaxoSmithKline Sierra Leone is committed to creating a diverse workforce and an inclusive environment. We do not discriminate on the basis of race, color, religion, gender, sexual orientation, age, disability, or any other protected characteristic. All qualified applicants will receive consideration for employment without regard to any such factor.