Senior Pharmaceutical Regulatory Affairs Specialist Job Vacancy in Beledweyne, Somalia – Healthcare & Life Sciences

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Specialist

Company: Pfizer Inc.

Location: Beledweyne, Somalia

Experience: 7+ years

Education: Doctor of Pharmacy (PharmD) or PhD in Pharmacology

Employment Type: Full-time

Industry: Healthcare & Life Sciences

Department: Regulatory Affairs

Salary: 4,500,000 – 6,200,000 SSP

Vacancies: 1

Company Overview

Pfizer Inc. is a global leader in the pharmaceutical industry, dedicated to discovering, developing, and manufacturing breakthrough medicines and vaccines that improve people’s lives. As a pioneer in biotechnology, we strive to set new standards in healthcare through relentless innovation and scientific excellence. Our mission is to deliver transformative treatments for patients facing the most challenging diseases worldwide. By joining our team, you become part of a legacy of scientific breakthroughs that have shaped modern medicine. We are currently expanding our footprint in East Africa to address critical healthcare needs, creating significant career opportunities in Somalia for highly skilled professionals.

Our commitment to excellence extends beyond the laboratory. We invest heavily in research and development to ensure that every product meets the highest safety and efficacy standards. As we grow, we continue to seek talent that shares our passion for science and our dedication to patient outcomes. For more information on our global initiatives, visit https://somaliajobsearch.com.

Job Overview

We are seeking a highly experienced Senior Pharmaceutical Regulatory Affairs Specialist to lead our regulatory strategy and compliance efforts in the region. This role is critical in ensuring that all pharmaceutical products, clinical trials, and manufacturing processes adhere to both local Somali health regulations and international standards set by the WHO and EMA. The successful candidate will act as the primary liaison between the company and national health authorities, navigating complex legal frameworks to facilitate the timely market entry of life-saving medications. This is a high-impact role that requires a deep understanding of drug development lifecycles and a proactive approach to regulatory intelligence.

This position offers a unique chance to influence healthcare delivery in the region. If you are looking for employment in Somalia within a world-class scientific environment, this is an unparalleled opportunity. You will manage complex dossiers, oversee post-market surveillance, and ensure that our entire supply chain remains compliant with evolving pharmaceutical laws.

Key Responsibilities

• Lead the preparation and submission of comprehensive regulatory dossiers for new drug applications and variations.
• Act as the primary point of contact for the Ministry of Health and other regulatory bodies in Somalia.
• Monitor and interpret changes in local and international pharmaceutical regulations to ensure continuous compliance.
• Collaborate with R&D and manufacturing teams to ensure all product documentation meets stringent quality standards.
• Oversee the lifecycle management of existing products, including renewals and safety updates.
• Provide expert guidance on clinical trial protocols and regulatory requirements for new therapeutic areas.
• Conduct regular audits of internal processes to ensure adherence to Good Manufacturing Practices (GMP).

Required Skills

• Expert knowledge of international regulatory guidelines (ICH, FDA, EMA) and local Somali health laws.
• Exceptional technical writing skills for the preparation of complex regulatory documents.
• Strong analytical thinking and the ability to interpret complex scientific data.
• Advanced negotiation and communication skills for interacting with government officials.
• Project management expertise to handle multiple regulatory submissions simultaneously.
• High level of attention to detail and commitment to quality assurance.

Education

A minimum of a Doctor of Pharmacy (PharmD), a PhD in Pharmacology, or a Master’s degree in Regulatory Affairs from a recognized international university is mandatory. Advanced certification in Clinical Research or Quality Management is highly preferred.

Experience

Candidates must possess a minimum of 7 years of professional experience in pharmaceutical regulatory affairs, preferably within a multinational pharmaceutical corporation. Proven experience in navigating the regulatory landscape of East African markets is a significant advantage. You should have a track record of successful drug registrations and interactions with national health authorities.

Salary

The monthly salary for this position is highly competitive, ranging from 4,500,000 SSP to 6,200,000 SSP, depending on the candidate’s expertise and previous experience in the sector.

Benefits

• Comprehensive health and dental insurance coverage for the employee and immediate family.
• Performance-based annual bonuses and long-term incentive plans.
• Generous paid time off and parental leave policies.
• Subsidized wellness programs and mental health support services.
• Professional development allowance for advanced certifications and conferences.

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Training

• Continuous professional development through Pfizer’s internal Global Regulatory Academy.
• Specialized training on updated WHO regulatory standards and local compliance updates.
• Leadership development programs for senior-level management roles.

Working Environment

The working environment is professional, highly collaborative, and science-driven. While the role is primarily office-based in our Beledweyne regional hub, it requires occasional travel to government offices and manufacturing sites. We foster a culture of integrity, diversity, and scientific rigor, ensuring that every team member feels empowered to contribute to our global mission of improving human health.

Application Process

Interested candidates who meet the specified requirements should submit their updated CV and a cover letter detailing their regulatory expertise through our official career portal. We are looking for individuals who are passionate about healthcare innovation and are eager to contribute to the growing pharmaceutical sector in the region. Please note that only shortlisted candidates will be contacted for interviews. For more job vacancies in Somalia, please visit our career page regularly.

For additional career opportunities in various sectors, visit https://zambiajobssearch.com/.

Equal Opportunity Statement

Pfizer 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, marital status, veteran status, or disability status.