Senior Pharmaceutical Regulatory Affairs Specialist Job Vacancy in Wau, South Sudan – Healthcare & Life Sciences

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Specialist

Company: Pfizer South Sudan

Location: Wau, South Sudan

Experience: 7+ years

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

Employment Type: Full-time

Industry: Healthcare & Life Sciences

Department: Regulatory Affairs

Salary: 1,200,000 – 2,500,000 SSP

Vacancies: 1

Company Overview

Pfizer is a global leader in the pharmaceutical industry, dedicated to discovering, developing, and manufacturing innovative medicines and vaccines that improve the lives of patients worldwide. Our mission is to transform patient health through science and innovation. In South Sudan, we are committed to expanding access to life-saving treatments and ensuring that the highest standards of medical safety and efficacy are met across the region. As part of our global network, our local operations focus on bridging the gap between advanced biotechnology and community healthcare needs. We pride ourselves on a culture of integrity, excellence, and patient-centricity, making us one of the most sought-after employers for professionals seeking meaningful career opportunities in South Sudan.

Job Overview

We are seeking a highly skilled Senior Pharmaceutical Regulatory Affairs Specialist to lead our compliance and registration efforts in the Western Bahr el Ghazal region. This critical role involves navigating complex local and international regulatory frameworks to ensure that all pharmaceutical products are registered, labeled, and distributed in strict accordance with South Sudanese health laws and international standards. The successful candidate will act as the primary liaison between the company and national health authorities, ensuring that our pipeline of innovative medicines reaches the people who need them most. This is a high-impact role that requires a deep understanding of clinical data, dossier preparation, and post-market surveillance. For those looking for professional growth, this position offers unparalleled exposure to global regulatory standards. You can learn more about our global mission at https://southsudanjobsearch.com.

Key Responsibilities

• Lead the preparation and submission of comprehensive dossiers for new drug applications to local health authorities.
• Ensure all pharmaceutical labeling, packaging, and promotional materials comply with national regulatory requirements.
• Monitor changes in local healthcare legislation and provide strategic guidance to internal stakeholders.
• Coordinate with clinical teams to ensure all regulatory documentation supports the safety and efficacy profiles of products.
• Manage post-market surveillance activities and report any adverse events to the relevant authorities immediately.
• Maintain meticulous records of all regulatory interactions and approvals to ensure audit readiness.

Required Skills

• Advanced knowledge of pharmaceutical regulatory processes and international compliance standards.
• Exceptional technical writing skills for the preparation of complex scientific dossiers.
• Strong analytical skills to interpret clinical trial data and regulatory guidelines.
• Excellent communication and negotiation skills for interacting with government officials.
• High level of attention to detail regarding legal and medical documentation.

Education

A Doctor of Pharmacy (PharmD), Master of Science in Regulatory Affairs, or a PhD in Pharmacology or a related life sciences field is mandatory for this position.

Experience

Candidates must possess a minimum of 7 years of experience in pharmaceutical regulatory affairs, preferably within a multinational pharmaceutical corporation. Proven experience in navigating the regulatory landscape of East African markets is highly desirable.

Salary

The monthly salary for this position ranges from 1,200,000 SSP to 2,500,000 SSP, depending on the candidate’s expertise and previous experience in the sector.

Benefits

• Comprehensive health and life insurance coverage.
• Performance-based annual bonuses.
• Professional development and continuous education allowances.
• Generous annual leave and paid sick leave.
• Commuter and relocation assistance for qualified candidates.

Training

Successful candidates will undergo intensive training on Pfizer’s global compliance protocols and specialized training on local South Sudanese health regulations. We also provide access to international regulatory certification programs. For more information on regional job trends, visit https://malawijobsearch.com/.

Working Environment

This role is primarily based in our Wau regional office, with occasional travel to Juba or other regional hubs for meetings with health officials. The environment is professional, fast-paced, and highly collaborative, requiring a balance of independent research and team-based strategic planning. We foster a culture of scientific rigor and ethical excellence.

Application Process

Interested candidates should submit their updated CV and a cover letter detailing their regulatory expertise through our official recruitment portal. Please ensure all certifications are ready for verification upon request. For more career opportunities in South Sudan, please monitor our portal regularly. You can also find similar roles across the continent at https://rwandajobsearch.com/job-vacancy-in-rwanda/.

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, or disability status.