Regulatory Affairs Specialist Job Vacancy in Kericho, Kenya – Pharmaceuticals

Job Description

Position: Regulatory Affairs Specialist

Company: Pfizer Kenya

Location: Kericho, Kenya

Experience: 3-5 years in pharmaceutical regulatory affairs

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

Employment Type: Full-time

Industry: Pharmaceuticals

Department: Regulatory Affairs

Salary: SSP 150,000 – 250,000 per month

Vacancies:1

Company Overview

Pfizer Kenya is a leading global pharmaceutical company dedicated to improving health outcomes across the continent. With a strong presence in Kenya for over two decades, Pfizer Kenya combines cutting‑edge research, innovative medicines, and a commitment to community health. The company operates state‑of‑the‑art manufacturing facilities, robust distribution networks, and collaborative partnerships with local health ministries. As part of Pfizer’s worldwide mission, the Kenya branch offers dynamic career pathways, fostering professional growth while contributing to the nation’s healthcare advancement. This role supports Pfizer’s vision of delivering breakthrough therapies and aligns with the growing demand for skilled regulatory professionals in the Kenyan market, making it a prime opportunity among Kenya Jobs and Jobs in Kenya.

Job Overview

The Regulatory Affairs Specialist will be responsible for ensuring that all Pfizer products comply with Kenyan regulatory requirements and international standards. This includes preparing and submitting dossiers, liaising with the Pharmacy and Poisons Board, and monitoring changes in legislation that affect product registration and post‑marketing obligations. The specialist will work closely with cross‑functional teams, including Clinical Development, Quality Assurance, and Marketing, to guarantee seamless product launches and sustained compliance. The role is central to Pfizer’s commitment to safety, efficacy, and regulatory excellence, offering a unique platform for career development within the pharmaceutical sector. For more information about Pfizer Kenya and to explore other Career Opportunities in Kenya, visit Kenya Job Search.

Key Responsibilities

• Prepare, review, and submit regulatory dossiers for new product registrations, variations, and renewals in Kenya.
• Maintain ongoing communication with the Pharmacy and Poisons Board and other relevant authorities.
• Monitor and interpret local and international regulatory guidelines, ensuring timely updates to internal policies.
• Collaborate with R&D, Quality, and Commercial teams to align product development with regulatory expectations.
• Provide regulatory strategy input for product lifecycle management and market expansion.
• Conduct internal audits and support external inspections to verify compliance.
• Develop and deliver regulatory training sessions for internal stakeholders.
• Prepare risk assessments and manage post‑marketing surveillance documentation.

Required Skills

• In‑depth knowledge of Kenyan pharmaceutical regulations and ICH guidelines.
• Strong analytical and problem‑solving abilities.
• Excellent written and verbal communication skills in English; proficiency in Swahili is an advantage.
• Ability to manage multiple projects and meet strict deadlines.
• Proficiency with regulatory submission software and document management systems.
• Collaborative mindset with experience working in cross‑functional teams.

Education

A Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related 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 a minimum of three to five years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with a focus on product registration and compliance in Kenya or other East African markets.

Salary

The position offers a competitive salary range of SSP 150,000 to 250,000 per month, commensurate with experience and qualifications. Additional performance‑based incentives may be provided.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with employer contributions.
• Paid annual leave, sick leave, and public holidays.
• Professional development allowance for certifications and conferences.
• Employee assistance program and wellness initiatives.

Training

• On‑boarding program covering Pfizer’s global regulatory framework and local compliance requirements.
• Continuous learning modules on emerging regulatory trends and digital submission tools.
• Mentorship opportunities with senior regulatory leaders across Pfizer’s global network.

Working Environment

Pfizer Kenya provides a modern, collaborative workspace in Kericho, equipped with the latest technology and resources to support regulatory activities. The culture emphasizes innovation, integrity, and a commitment to improving health outcomes, fostering an environment where employees can thrive and contribute meaningfully to the company’s mission.

Application Process

Interested candidates should submit their application through the online portal on the Pfizer Kenya careers page. Ensure your resume highlights relevant regulatory experience, education, and any certifications. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for interviews. This is a prime Hiring in Kenya opportunity for professionals seeking to advance their regulatory career.

Equal Opportunity Statement

Pfizer Kenya is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, religion, disability, or sexual orientation. All qualified applicants will receive consideration for employment without discrimination.