Regulatory Affairs Specialist Job Vacancy in Tubmanburg, Liberia – Pharmaceuticals

Job Description

Position: Regulatory Affairs Specialist

Company: Pfizer Inc.

Location: Tubmanburg, Liberia

Experience: 3-5 years in regulatory affairs within the 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: SSP 2,500,000 – SSP 4,500,000 per month

Vacancies:1

Company Overview

Pfizer Inc. is a global leader in innovative medicines, vaccines, and consumer health products, committed to improving health outcomes worldwide. With a strong presence across Africa, Pfizer has established partnerships with local health ministries, distributors, and research institutions to ensure access to high‑quality pharmaceuticals. In Liberia, Pfizer collaborates with the Ministry of Health to support disease prevention programs, capacity building, and the introduction of life‑saving treatments. The company’s dedication to scientific excellence, ethical standards, and community impact makes it a preferred employer for professionals seeking meaningful careers in the pharmaceutical sector. As part of its expansion strategy, Pfizer is investing in regulatory infrastructure and talent development in Tubmanburg, creating new pathways for career growth and contributing to the nation’s health ecosystem.

Joining Pfizer means becoming part of a diverse, inclusive, and forward‑thinking organization that values integrity, collaboration, and continuous learning. Employees benefit from a supportive work environment that encourages innovation, professional development, and a balanced lifestyle. Pfizer’s commitment to corporate social responsibility is reflected in its community outreach initiatives, scholarships, and health education programs that align with national development goals. For candidates looking for dynamic career opportunities, Pfizer offers a platform to make a tangible difference in the lives of Liberians while advancing their own expertise in regulatory affairs.

Job Overview

The Regulatory Affairs Specialist will play a pivotal role in ensuring that Pfizer’s products comply with all applicable local and international regulations, guidelines, and standards. Based in Tubmanburg, the specialist will work closely with cross‑functional teams, including Quality Assurance, Clinical Development, and Marketing, to prepare and submit regulatory dossiers, maintain product registrations, and liaise with the Liberia Food and Drug Authority (LFDA). This position is essential for safeguarding product integrity, accelerating market access, and supporting Pfizer’s mission to deliver innovative therapies to patients across Liberia. The role offers exposure to a broad range of regulatory activities, from initial product filings to post‑approval monitoring, providing a comprehensive understanding of the pharmaceutical regulatory landscape.

As part of Pfizer’s commitment to hiring in Liberia, the Regulatory Affairs Specialist will also contribute to capacity‑building initiatives, mentoring junior staff and participating in stakeholder workshops aimed at strengthening the country’s regulatory framework. The successful candidate will be instrumental in driving compliance excellence, fostering relationships with health authorities, and ensuring that Pfizer’s products meet the highest safety and efficacy standards. This is a unique opportunity to be at the forefront of pharmaceutical regulation in a rapidly evolving market, supporting both corporate objectives and national health priorities.

Key Responsibilities

• Prepare, review, and submit regulatory dossiers for new product registrations, variations, and renewals in accordance with LFDA requirements.
• Maintain and update product registration files, ensuring all documentation is current and compliant.
• Act as the primary liaison between Pfizer and the Liberia Food and Drug Authority, facilitating clear communication and timely resolution of regulatory queries.
• Collaborate with Quality Assurance, Clinical Development, and Marketing teams to gather necessary data and ensure alignment with regulatory expectations.
• Monitor changes in local and international regulatory guidelines, providing proactive recommendations to internal stakeholders.
• Support post‑approval activities, including product labeling updates, adverse event reporting, and compliance audits.
• Participate in training sessions and workshops to enhance regulatory knowledge across the organization.
• Contribute to the development of standard operating procedures (SOPs) for regulatory processes.

Required Skills

• Strong knowledge of pharmaceutical regulations, guidelines, and submission processes in Liberia and the African region.
• Excellent written and verbal communication skills, with the ability to convey complex regulatory information clearly.
• Detail‑oriented mindset with strong analytical and problem‑solving abilities.
• Proficiency in regulatory software tools and Microsoft Office Suite.
• Ability to work independently and collaboratively in a multicultural environment.
• Effective time management and ability to prioritize multiple projects under tight deadlines.

Education

A Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline is required. A Master’s degree or professional certification in regulatory affairs (e.g., RAC) is highly desirable and will be considered an advantage during the selection process.

Experience

Applicants must have 3‑5 years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to African regulatory authorities. Experience in preparing dossiers for product registration, variation, and renewal is essential.

Salary

The compensation package ranges from SSP 2,500,000 to SSP 4,500,000 per month, commensurate with experience and qualifications. The package includes performance‑based incentives and benefits aligned with Pfizer’s global standards.

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 Pfizer’s regulatory processes, compliance standards, and corporate culture.
• Continuous learning opportunities through internal e‑learning platforms and external workshops.
• Mentorship from senior regulatory professionals within the global network.

Working Environment

Pfizer’s Tubmanburg office offers a modern, collaborative workspace equipped with the latest technology to support regulatory activities. The environment promotes teamwork, innovation, and a healthy work‑life balance, reflecting Pfizer’s commitment to employee well‑being and productivity.

Application Process

Interested candidates should submit their updated resume and a cover letter outlining their relevant experience through the online portal at https://liberiajobsearch.com/. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. Pfizer encourages applications from qualified individuals of all backgrounds.

Equal Opportunity Statement

Pfizer 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, sex, sexual orientation, gender identity, national origin, disability, or veteran status.