Regulatory Affairs Specialist Job Vacancy in Benguela, Angola – Pharmaceuticals
Job Description
Position: Regulatory Affairs Specialist
Company: Pfizer
Location: Benguela, Angola
Experience: 3-5 years in pharmaceutical regulatory affairs
Education: Bachelor’s degree in Pharmacy, Life Sciences or related field
Employment Type: Full-time
Industry: Pharmaceuticals
Department: Regulatory Affairs
Salary: SSP 250,000 – 400,000 per month
Vacancies:1
Company Overview
Pfizer is a global leader in innovative medicines, vaccines, and consumer health products, operating in more than 150 countries. In Angola, Pfizer is committed to improving health outcomes by providing high‑quality pharmaceuticals and supporting local healthcare infrastructure. Our presence in Benguela strengthens our ability to serve the central region of Angola, fostering partnerships with government agencies, hospitals, and private clinics. As part of our growth strategy, we are expanding our regulatory team to ensure compliance with national and international standards, creating a vibrant career path for professionals seeking to make a difference in the pharmaceutical sector. This role contributes directly to Angola Jobs, Jobs in Angola, and the broader mission of enhancing public health.
Job Overview
The Regulatory Affairs Specialist will lead the preparation, submission, and maintenance of product dossiers with Angola’s National Institute of Medicines (INMAS). You will act as the primary liaison between Pfizer and regulatory authorities, ensuring that all pharmaceutical products meet local compliance requirements while aligning with global standards. This position offers a unique opportunity to influence market access strategies, support product launches, and safeguard patient safety across the region. For more information about our career portal, visit our main website.
Key Responsibilities
- Prepare and submit registration dossiers for new and existing pharmaceutical products to INMAS.
- Maintain up‑to‑date regulatory intelligence on Angola’s health legislation and guidelines.
- Coordinate cross‑functional teams, including Clinical, Quality, and Marketing, to gather required documentation.
- Respond to queries from regulatory authorities and manage post‑approval variations.
- Develop and implement regulatory strategies that support timely market entry.
- Ensure compliance with Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).
- Provide regulatory training and guidance to internal stakeholders.
Required Skills
- Strong knowledge of Angola’s pharmaceutical regulatory framework.
- Excellent written and verbal communication in Portuguese and English.
- Analytical mindset with attention to detail and ability to interpret complex guidelines.
- Proficiency in regulatory submission software and document management tools.
- Project management skills with ability to meet tight deadlines.
- Collaborative approach and ability to work with multidisciplinary teams.
Education
A Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related life‑science discipline is required. Advanced degrees (MSc or PhD) or certifications in regulatory affairs are highly desirable and will be considered an advantage.
Experience
Applicants must have 3‑5 years of hands‑on experience in regulatory affairs within the pharmaceutical industry, preferably with exposure to African markets. Experience with product lifecycle management and submission of dossiers for both generic and innovative medicines is essential.
Salary
The compensation package ranges from SSP 250,000 to SSP 400,000 per month, commensurate with experience and qualifications. The package includes performance‑based bonuses and comprehensive benefits.
Benefits
- Health insurance covering employee and dependents.
- Retirement savings plan with company matching.
- Paid parental and annual leave.
- Transportation allowance for commuting in Benguela.
- Employee assistance program and wellness initiatives.
Training
- Continuous professional development through Pfizer’s global learning platform.
- Access to regulatory conferences and workshops across Africa.
- Mentorship program with senior regulatory leaders.
- On‑the‑job training in dossier preparation and submission processes.
Working Environment
Our Benguela office offers a modern, collaborative workspace equipped with the latest technology. Employees enjoy a culture that values innovation, integrity, and inclusion, fostering a supportive environment for personal and professional growth.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining their regulatory experience through our online portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for virtual interviews.
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https://southafricajobsearch.com/
Equal Opportunity Statement
Pfizer 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, sexual orientation, or disability. Our hiring practices support the principles of fairness and meritocracy, ensuring that every candidate has an equal chance to succeed.
