Regulatory Affairs Specialist Job Vacancy in Jalalaqsi, Somalia – Pharmaceuticals

Job Description

Position:Regulatory Affairs Specialist

Company:Pfizer

Location:Jalalaqsi, Somalia

Experience:3-5 years in regulatory affairs within pharmaceutical industry

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

Employment Type:Full-time

Industry:Pharmaceuticals

Department:Regulatory Affairs

Salary:5,000,000 – 8,000,000 SSP per month

Vacancies:1

Company Overview

Pfizer is a globally recognized leader in innovative medicines, vaccines, and consumer health products. With a presence in more than 150 countries, Pfizer is committed to improving health outcomes worldwide, including emerging markets such as Somalia. The company’s mission to deliver breakthroughs that change patients’ lives drives a culture of scientific excellence, ethical standards, and community engagement. As part of its expansion strategy, Pfizer is establishing a regulatory hub in Jalalaqsi to support local and regional compliance, ensuring that high‑quality pharmaceutical products reach patients safely and efficiently. This initiative creates a range of Somalia Jobs that contribute to the nation’s healthcare infrastructure and economic development.

Job Overview

The Regulatory Affairs Specialist will play a pivotal role in managing the submission, review, and maintenance of product dossiers for Pfizer’s portfolio in Somalia and the Horn of Africa region. Reporting to the Regional Regulatory Manager, the specialist will collaborate with cross‑functional teams, including Clinical Development, Quality Assurance, and Marketing, to ensure compliance with local regulations and international standards. This position offers a unique opportunity to be part of a dynamic team that influences public health outcomes while advancing your career in a fast‑growing market. For more information about Pfizer’s presence in Somalia, visit https://somaliajobsearch.com/.

Key Responsibilities

• Prepare, review, and submit regulatory applications, variations, and renewals to the Somali Ministry of Health and related authorities.
• Maintain up‑to‑date product dossiers, ensuring all documentation meets local and international guidelines.
• Coordinate with internal stakeholders to gather scientific data, labeling, and safety information required for submissions.
• Monitor regulatory changes in Somalia and the broader East African region, providing strategic guidance to the business.
• Serve as the primary point of contact for regulatory agencies, facilitating inspections and audits.
• Develop and implement regulatory strategies that align with Pfizer’s global standards and local market needs.
• Support post‑marketing surveillance activities, including adverse event reporting and product lifecycle management.

Required Skills

• In‑depth knowledge of Somali pharmaceutical regulations and WHO guidelines.
• Strong analytical and problem‑solving abilities with attention to detail.
• Excellent written and verbal communication skills in English; proficiency in Somali is an advantage.
• Ability to work collaboratively across multidisciplinary teams and manage multiple projects simultaneously.
• Proficiency with regulatory submission software and Microsoft Office Suite.

Education

A minimum of a Bachelor’s degree in Pharmacy, Chemistry, Pharmacology, or a related scientific discipline is required. A Master’s degree or professional certification in regulatory affairs (e.g., RAC) is highly desirable and will be considered an asset 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 emerging markets. Experience in preparing dossiers for new drug applications, variations, and renewals is essential.

Salary

The compensation package ranges from 5,000,000 to 8,000,000 SSP per month, commensurate with experience and qualifications. The package includes performance‑based incentives and statutory benefits.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan aligned with Somali labor regulations.
• Paid annual leave and sick leave.
• Professional development allowance for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• Onboarding program covering Pfizer’s global compliance framework and local regulatory landscape.
• Continuous learning modules on regulatory intelligence, pharmacovigilance, and quality systems.
• Mentorship opportunities with senior regulatory leaders across Pfizer’s global network.

Working Environment

The role is based in a modern office in Jalalaqsi, equipped with state‑of‑the‑art IT infrastructure and collaborative workspaces. Pfizer promotes a culture of inclusion, safety, and innovation, encouraging employees to share ideas and drive continuous improvement.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the online portal on the Pfizer Careers page. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for virtual interviews.

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, gender, sexual orientation, gender identity, national origin, disability, or veteran status. This commitment supports the broader goal of fostering Employment in Somalia and promoting Career Opportunities in Somalia for all talent.