Organization Name: Cospharm Pharmaceuticals
Job Title: Regional Regulatory Affairs Officer (Harare)
Key Responsibilities
- **Dossier Management & Submissions:** Compilation and continuous filing of new dossiers in concerned territories. Ensure all submissions meet specific national regulatory requirements
- **Product registration & Lifecycle Maintenance:** Extract registrations of filed products through response submission to NRAs. Also manage post-registration amendments where required and necessary.
- Actively engage with suppliers to ensure all responses to regulatory queries are submitted accurately and on time.
- **Data managment:** Maintain an up-to-date regional dossier database covering concerned territories.
- **Pharmacovigilance (PV) & Compliance System:** assist and ensure a robust system for pharmacovigilance.
- Collaborate with Business Development and Operations based on organizational needs and business direction.
- **Stakeholder Relations:** Build and maintain professional relationships with National Regulatory Authorities (NRAs).
Requirements
- 1st degree in Pharmacy or Life Science
- At least 2-3 years working in pharmaceutical regulatory industry (Experience in regional / multi-country RA industry is an added advantage)
- Understanding the intersection of Regulatory affairs, Pharmacovigilance and product lifecycle management
- Be knowledgeable of the regulatory requirements across SADC and other African countries
How to Apply
Email: [email protected] (Email your CV indicating the position in the subject line)
Due date for applications: 15 April 2026
Due date for applications: 15 April 2026
About the Company
Cospharm Pharmaceuticals (Pvt) Ltd is a prominent diversified pharmaceutical company operating within Zimbabwe, established in 1996. Headquartered in Harare, the company specializes in the importation, marketing, sales, and distribution of a wide range of quality pharmaceuticals, medical devices, reagents, and other essential healthcare products. As a leading distributor and importer, Cospharm Pharmaceuticals plays a crucial role in ensuring access to affordable and safe medicines across the Zimbabwean market, contributing significantly to the nation's healthcare sector.
Committed to better healthcare.
Website: http://www.cospharm.co
Job Summary
Frequently Asked Questions
What qualifications and certifications are typically required for a Regional Regulatory Affairs Officer role in Zimbabwe?
A Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or a related life science field is usually essential. Many employers also prefer candidates with post-graduate qualifications or specific certifications in regulatory affairs, demonstrating a strong understanding of local and regional pharmaceutical regulations. Experience with Zimbabwe's Medicines Control Authority (MCAZ) guidelines is highly valued.
What are the common day-to-day responsibilities of a Regional Regulatory Affairs Officer in Zimbabwe's pharmaceutical sector?
Day-to-day tasks involve preparing, submitting, and maintaining product registration dossiers with regulatory bodies like MCAZ across the region. This includes ensuring compliance with local laws, managing product licenses, and providing regulatory support for product launches and post-market surveillance. Officers also monitor regulatory changes and update internal teams accordingly.
What should I expect regarding the work culture and expectations for this role in Zimbabwean pharmaceutical companies?
The work culture often emphasizes meticulous attention to detail, adherence to strict deadlines, and a strong sense of responsibility due to the critical nature of regulatory compliance. Collaboration with local and regional teams is common, requiring effective communication and adaptability to diverse regulatory landscapes within the region. Professionalism and ethical conduct are highly valued.
What are the typical career progression and growth paths for a Regulatory Affairs Officer in Zimbabwe?
Career progression often leads to Senior Regulatory Affairs Officer, Regulatory Affairs Manager, or even regional leadership roles within the pharmaceutical industry. Opportunities might also extend to specializing in specific product categories or moving into quality assurance or pharmacovigilance. Continuous professional development and staying updated with regulatory changes are key for advancement.
What common benefits are usually offered for a role like the Regional Regulatory Affairs Officer in Zimbabwe?
Typical benefits often include medical aid coverage, a pension scheme, and standard annual leave as mandated by Zimbabwean labour laws. Some companies may also offer performance-based bonuses, fuel allowances, or professional development support. These benefits aim to attract and retain skilled professionals in the competitive pharmaceutical sector.