Senior Pharmaceutical Regulatory Affairs Specialist Job Vacancy in Gbarbo, Liberia – Healthcare & Life Sciences

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Specialist

Company: Pfizer Liberia

Location: Gbarbo, Liberia

Experience: 7+ years of specialized regulatory experience

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

Employment Type: Full-time

Industry: Healthcare & Life Sciences

Department: Regulatory Affairs & Compliance

Salary: 450,000 – 750,000 SSP

Vacancies: 1

Company Overview

Pfizer Liberia is a leading force in the pharmaceutical landscape, dedicated to delivering life-changing medicines and breakthroughs that make a difference to patients every day. As a global leader in healthcare, our mission is to transform patient health through science and innovation. In Liberia, we are committed to improving access to essential medications and ensuring that the highest standards of medical safety and efficacy are met across all our operations. We pride ourselves on a culture of excellence, integrity, and scientific rigor, making us one of the most sought-after employers for professionals seeking meaningful career opportunities in Liberia.

Job Overview

We are seeking a highly skilled Senior Pharmaceutical Regulatory Affairs Specialist to join our growing team in Gbarbo. This critical role involves navigating the complex landscape of national and international pharmaceutical regulations to ensure that all our products are compliant with local laws and global standards. You will act as a primary liaison between the company and the Liberia Medicines and Drugs Control Authority (LMDCA). This position is vital for our mission to bring innovative treatments to the Liberian market safely and efficiently. For more information on our global mission, visit liberiajobsearch.com.

Key Responsibilities

• Lead the preparation and submission of dossiers for new drug applications and product variations.
• Ensure all marketing and labeling materials comply with local regulatory requirements.
• Monitor changes in pharmaceutical legislation and provide strategic guidance to internal stakeholders.
• Coordinate with clinical research teams to ensure regulatory compliance during trials.
• Manage post-market surveillance data and report safety concerns to relevant authorities.
• Oversee the lifecycle management of existing product registrations.

Required Skills

• Expert knowledge of pharmaceutical regulatory frameworks and compliance standards.
• Strong analytical skills with the ability to interpret complex scientific data.
• Exceptional communication skills for interacting with government officials and internal teams.
• Project management expertise to handle multiple submission timelines simultaneously.
• High attention to detail regarding technical documentation and legal requirements.

Education

A professional doctorate in Pharmacy (PharmD), a PhD in Pharmacology, or a Master’s degree in Regulatory Affairs from an accredited institution is mandatory for this role.

Experience

Candidates must possess a minimum of 7 years of experience in pharmaceutical regulatory affairs, preferably within a multinational pharmaceutical corporation. Proven experience in dealing with West African regulatory bodies is highly advantageous. You can find similar high-level roles by checking namibiajobsearch.com for regional insights.

Salary

The offered salary for this position ranges from 450,000 SSP to 750,000 SSP, depending on the candidate’s expertise and qualifications.

Benefits

• Comprehensive health and dental insurance coverage.
• Performance-based annual bonuses.
• Generous paid time off and parental leave.
• Retirement savings plan contributions.
• Professional development and certification reimbursement.

Training

• Advanced Regulatory Intelligence workshops.
• Leadership and management training programs.
• Specialized pharmaceutical compliance seminars.

Working Environment

The working environment is a professional, high-stakes office setting that requires a balance of independent research and collaborative team meetings. While the role is primarily office-based in Gbarbo, occasional travel to regional offices or regulatory headquarters may be required. We offer a supportive atmosphere that encourages continuous learning and scientific inquiry. If you are looking for employment in Liberia, this is a premier opportunity to join a world-class organization.

Application Process

Interested candidates should submit their updated CV and a cover letter detailing their regulatory expertise through our official portal. Please note that we only accept applications through verified channels. For more diverse job listings across the continent, please visit somaliajobsearch.com.

Equal Opportunity Statement

Pfizer Liberia is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment is decided on the basis of qualifications, merit, and business needs, regardless of race, religion, color, or national origin.