Job Summary
- Type: full-time
- Location: Gaborone
- Category: Pharmaceutical
- Closing Date: 2026-08-21
Key Responsibilities
- hold accountability for the technical and regulatory integrity of the manufacturing site and its product portfolio
- bring and sustain the facility at a compliance standard capable of withstanding inspection by the Botswana Medicines Regulatory Authority (BoMRA), the ZaZiBoNa joint inspectorate and WHO Prequalification
- lead the closure of regulatory findings and Corrective and Preventive Action (CAPA) programmes
- direct dossier compilation and lifecycle management across SADC and EAC markets
- establish, from first principles, a site Quality Management System capable of certification and of sustaining national and international market authorisations
Requirements
- A minimum of ten (10) years’ post-registration experience in medicines regulation and industrial pharmacy field.
- Demonstrated performance in GMP and GSDP audits and gap assessments across countries in Africa and Asia, comprising physical, virtual and desktop inspection modalities.
- Industrial or inspection competence across the full range of dosage forms general oral solids, sterile products including large volume parenterals, biologicals and vaccines, sensitising materials, and Quality Control Laboratories.
- Hands-on coordination of oral dosage technology transfer and in-house generic research and development.
- Development and implementation from the ground up of GMP- and GSDP-compliant Quality Management Systems, and participation in accreditation audits against ISO 9001, ISO/IEC 17020 and ISO/IEC 17025.
- Bachelor of Pharmacy (Honours) degree from a recognised university, and eligibility for immediate registration as a Pharmacist with the Botswana Health Professions Council.
- A Master’s degree in Pharmaceutical Sciences specialising in Regulatory Affairs (or a directly equivalent postgraduate qualification in medicines regulation).
- Postgraduate qualification or formal training in Monitoring and Evaluation of GMP and GSDP standards and regulations
- Ability to open and defend a technical position before a regulatory authority, a joint regional inspectorate and a board of directors with equal command.
- Proven record of building and mentoring regulatory and quality teams across multiple national markets.
How to Apply
Only shortlisted candidates will be contacted.
About the Company
Portfolio Pharmaceuticals Botswana (Pty) Ltd. stands as a significant contributor to the nation's healthcare industry. The company is recognized as a leader in pharmaceutical drug manufacturing and packaging, supplying essential medical products within Botswana. As an integral member of the Avacare Health Group, it leverages a broader network while focusing on local operations. Through its dedicated facilities, Portfolio Pharmaceuticals Botswana plays a vital role in strengthening the country's pharmaceutical supply chain. This commitment underscores its importance in ensuring access to quality medicines across Botswana.
A leader in pharmaceutical drug manufacturing and packaging in Botswana.
Website: http://portfoliopharma.co.bw/
Frequently Asked Questions
What are the typical educational qualifications and certifications needed for a Pharmaceutical Technology Transfer and Industrialisation Specialist in Botswana?
This role usually requires a Bachelor's or Master's degree in Pharmacy, Pharmaceutical Science, Chemical Engineering, or a related scientific field. Relevant certifications in Good Manufacturing Practices (GMP), project management, or quality assurance are also highly valued by employers in Botswana.
What are the common day-to-day responsibilities for a Specialist in Pharmaceutical Technology Transfer and Industrialisation in Botswana?
Daily tasks often involve coordinating technology transfer projects, ensuring compliance with local and international regulatory standards for pharmaceutical products. You would also be involved in optimizing manufacturing processes and overseeing the industrialization of new drug formulations.
What is the typical work culture like for a Pharmaceutical Technology Transfer Specialist in Botswana's pharmaceutical industry?
The work culture in Botswana's pharmaceutical sector emphasizes strict adherence to quality standards, regulatory compliance, and collaborative teamwork. Professionals are expected to be meticulous, adaptable, and committed to maintaining high levels of integrity and safety.
What are the realistic career progression opportunities for a Pharmaceutical Technology Transfer and Industrialisation Specialist in Botswana?
Successful specialists can advance into senior management positions such as Head of Manufacturing, Quality Assurance Manager, or R&D Director within pharmaceutical companies. Opportunities also exist to move into consultancy or regulatory affairs roles, leveraging their specialized expertise.
What kind of typical benefits package (e.g., leave, medical aid, pension) can a Specialist expect from a pharmaceutical employer in Botswana?
Employers in Botswana generally offer competitive benefits packages that include standard annual leave, a provident or pension fund, and comprehensive medical aid coverage. Some companies may also provide professional development opportunities and performance-based incentives.
What should job seekers highlight in their application, and what do employers in Botswana look for in this specialist role?
Job seekers should highlight strong technical expertise in pharmaceutical manufacturing, quality systems, and regulatory compliance, particularly experience with technology transfer protocols. Employers in Botswana seek candidates with proven problem-solving abilities, excellent communication skills, and a commitment to maintaining high industry standards.