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

Job Description

Position: Senior Pharmaceutical Regulatory Affairs Specialist

Company: Pfizer Liberia

Location: Monrovia, Liberia

Experience: 7+ years

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

Employment Type: Full-time

Industry: Healthcare & Life Sciences

Department: Regulatory Affairs

Salary: 450,000 – 750,000 SSP

Vacancies: 1

Company Overview

Pfizer Liberia is a leading force in the pharmaceutical sector, dedicated to transforming patient lives through groundbreaking science and innovative medical solutions. As a key player in the West African healthcare landscape, our mission is to ensure that life-saving medications and vaccines are accessible, safe, and effective for the population of Liberia. We operate at the intersection of cutting-edge biotechnology and public health necessity, working tirelessly to address some of the most challenging medical conditions in the region. Our commitment to excellence is reflected in our rigorous quality standards and our unwavering dedication to ethical medical practices. By joining our team, you become part of a global legacy of scientific innovation and a local mission of health equity. We are actively seeking top-tier talent to help us navigate the complex regulatory landscapes of the African continent, ensuring that every product we bring to market meets the highest international benchmarks of safety and efficacy. This is a premier opportunity for professionals looking for meaningful career opportunities in Liberia within a highly respected multinational corporation.

Job Overview

The Senior Pharmaceutical Regulatory Affairs Specialist will play a critical role in ensuring that all Pfizer products are compliant with both local Liberian health regulations and international standards. This position involves managing the lifecycle of pharmaceutical products, from initial clinical trial documentation to post-market surveillance. You will act as the primary liaison between the company and the Liberia Medicines and Health Products Regulatory Authority (LMHRA). This role requires a deep understanding of drug registration processes, labeling requirements, and safety reporting protocols. As we expand our footprint in West Africa, this position is vital for maintaining our reputation for integrity and compliance. We are looking for a strategic thinker who can navigate complex legal frameworks while facilitating the timely launch of new therapeutic options. For more information on global career trends, visit https://zimbabwejobsearch.com.

Key Responsibilities

• Lead the preparation and submission of dossiers for new drug applications to local regulatory bodies.
• Ensure all marketing and promotional materials comply with pharmaceutical advertising regulations.
• Monitor changes in local and international healthcare laws to ensure continuous organizational compliance.
• Coordinate with the clinical research team to manage regulatory requirements for ongoing trials.
• Oversee the lifecycle management of existing products, including renewals and variations.
• Collaborate with the quality assurance team to investigate and report any adverse drug reactions.
• Represent the company in meetings with government health officials and industry stakeholders.

Required Skills

• Expert knowledge of pharmaceutical regulatory frameworks and drug registration processes.
• Strong analytical skills with the ability to interpret complex scientific and legal documentation.
• Exceptional communication skills for interacting with government officials and internal stakeholders.
• High level of attention to detail regarding compliance and documentation standards.
• Project management expertise to handle multiple product registrations simultaneously.
• Strategic problem-solving abilities to navigate regulatory hurdles.

Education

Candidates must possess a terminal degree in Pharmacy (PharmD), Pharmacology, or a closely related life sciences field. A Master’s degree in Regulatory Affairs or a related legal field may be considered if accompanied by extensive industry experience.

Experience

A minimum of 7 years of experience in pharmaceutical regulatory affairs is required. Proven experience working within the African regulatory environment or with international pharmaceutical companies is highly preferred. Candidates should demonstrate a track record of successful product registrations and regulatory inspections.

Salary

The offered salary for this position ranges from 450,000 SSP to 750,000 SSP per annum, depending on the candidate’s expertise and experience level. This is a competitive package designed to attract the best talent in the industry.

Benefits

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

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Training

• Advanced Regulatory Compliance Certification.
• Leadership and Management Development Program.
• Specialized training on new pharmaceutical technologies.
• Internal workshops on international health standards.

Working Environment

The working environment is a professional, high-stakes office setting located in the heart of Monrovia. While the role is primarily office-based, it requires occasional travel to government offices and regional distribution centers. We foster a culture of scientific rigor, collaboration, and continuous learning. You will work alongside highly skilled scientists, medical professionals, and legal experts in a fast-paced, mission-driven environment. This is a prime example of employment in Liberia for those seeking high-level corporate responsibility.

Application Process

Interested candidates should submit their updated CV and a cover letter detailing their regulatory experience through our official recruitment portal. Please ensure all certifications are ready for verification upon request. We are currently hiring in Liberia and look forward to reviewing your application. For more job vacancy in Liberia listings, please check our portal regularly.

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Equal Opportunity Statement

Pfizer Liberia 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. We are dedicated to hiring the most qualified candidates to drive innovation in healthcare.