Regulatory Affairs Specialist Job Vacancy in Kakata, Liberia – Pharmaceuticals

Job Description

Position:Regulatory Affairs Specialist

Company:GlaxoSmithKline

Location:Kakata, Liberia

Experience:3-5 years in pharmaceutical regulatory affairs

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

Employment Type:Full-time

Industry:Pharmaceuticals

Department:Regulatory Affairs

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

Vacancies:1

Company Overview

GlaxoSmithKline (GSK) is a global healthcare company dedicated to improving the quality of life through innovative medicines, vaccines, and consumer healthcare products. With a strong commitment to research and development, GSK operates in more than 150 countries, delivering solutions that address some of the world’s most pressing health challenges. In Liberia, GSK has established a regional hub that supports the distribution of essential medicines, collaborates with local health authorities, and invests in community health programs. The company’s presence in Kakata reflects its strategic focus on expanding access to high‑quality pharmaceuticals across West Africa, creating a dynamic environment for professionals who are passionate about regulatory excellence and public health impact. This role offers a unique opportunity to contribute to GSK’s mission while gaining exposure to international regulatory standards and local market dynamics, making it an ideal career step for ambitious regulatory professionals.

Job Overview

The Regulatory Affairs Specialist will serve as the primary liaison between GSK’s global regulatory teams and Liberian health authorities, ensuring that all products meet local compliance requirements and international best practices. This position involves preparing and submitting dossiers, managing product registrations, and providing strategic guidance on regulatory pathways for new and existing products. The specialist will also monitor changes in legislation, advise cross‑functional teams on compliance implications, and support the launch of innovative therapies that address unmet medical needs in Liberia. By joining GSK’s regulatory team, you will play a pivotal role in safeguarding product quality, accelerating market access, and enhancing patient outcomes. For more information about GSK’s career opportunities, visit https://liberiajobsearch.com.

Key Responsibilities

• Prepare, compile, and submit regulatory dossiers for product registration, renewal, and variation in Liberia.
• Maintain up‑to‑date knowledge of Liberian pharmaceutical regulations, guidelines, and international standards such as ICH and WHO.
• Collaborate with R&D, Quality Assurance, and Commercial teams to ensure regulatory compliance throughout product lifecycle.
• Provide regulatory strategy recommendations to accelerate product launch timelines while maintaining safety and efficacy standards.
• Monitor and interpret legislative changes, advising internal stakeholders on impact and necessary actions.
• Develop and maintain a comprehensive regulatory intelligence database for Liberia and the West African region.
• Facilitate inspections and audits by health authorities, preparing required documentation and responding to queries.
• Support post‑marketing surveillance activities, ensuring timely reporting of adverse events and product updates.

Required Skills

• Strong understanding of pharmaceutical regulatory frameworks and submission processes.
• Excellent written and verbal communication skills in English; proficiency in French is an advantage.
• Analytical mindset with the ability to interpret complex regulatory documents.
• Proficiency in regulatory software tools and Microsoft Office Suite.
• Effective project management skills, capable of handling multiple dossiers simultaneously.
• Collaborative team player with the ability to influence cross‑functional partners.

Education

A minimum of a Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline is required. Candidates holding a Master’s degree or professional certifications such as RAC (Regulatory Affairs Certification) are highly preferred, reflecting a commitment to continuous professional development.

Experience

Applicants should possess 3‑5 years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to both local (Liberian) and international regulatory environments. Experience in product registration, dossier preparation, and interaction with health authorities is essential.

Salary

The position offers a competitive salary range of SSP 2,500,000 to 3,500,000 per month, commensurate with experience and qualifications. Performance‑based incentives and annual bonuses are also part of the compensation package.

Benefits

• Comprehensive health insurance covering medical, dental, and vision care.
• Retirement savings plan with employer contributions.
• Paid annual leave, sick leave, and public holidays.
• Professional development allowance for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• Onboarding program covering GSK’s regulatory processes, corporate culture, and compliance standards.
• Access to GSK’s global learning platform for continuous skill enhancement.
• Mentorship opportunities with senior regulatory leaders across the region.

Working Environment

GSK’s Kakata office provides a collaborative, inclusive, and modern workspace equipped with state‑of‑the‑art technology and resources. The company promotes a culture of safety, diversity, and innovation, encouraging employees to share ideas and drive positive change. Employees benefit from flexible working arrangements, fostering a healthy work‑life balance while meeting business objectives.

For insights into regional job markets, explore https://eswatinijobsearch.com/job-vacancy-eswatini/.

Application Process

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

Additional resources for job seekers can be found at https://moroccojobsearch.com/.

Equal Opportunity Statement

GlaxoSmithKline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.