A pharmaceutical manufacturing entity in is looking for talent to take up the position of Quality Assurance Manager and become an integral part of a high performing team.

The incumbent is to lead the continued development, implementation and maintenance of the quality management system supporting the production and development of good quality medicines and medical products, in accordance with the Botswana Medicines and Related Substances, national, and international guidelines and policies.

• Type: full-time
• Location: Gaborone
• Category: Quality Control
• Closing Date: 202 •••••• 10

Key Responsibilities

• through leadership of a small team at unit level, be responsible for providing technical and operational strategic direction to the quality assurance portfolio.interface and work closely with the Heads of Production and Quality Control and other support functions such as Engineering, Research & Development and Procurement and be responsible for effective QA support of cross-functional activities and coordination of the same.identify and establish appropriate quality standards, specifications and parameters for products; and communicate the quality standards and parameters to the QA team and other appropriate staff to ensure adherence and implementationwrite, revise and approve standard operating procedures for the facility, as necessary.
• The incumbent shall also support document control functionsprovide quality oversight for product manufacturing activities including review of executed batch records, batch release and change control processes associated with manufacturing activitieslead investigations related to product manufacturing activities, product marketing information and complaints, and non-compliances.support the Regulatory Affairs function, and where necessary, liaise with BOMRA, the national regulatory Authority.
• Oversee external and internal quality inspections and closing of CAPA

Requirements

• A bachelor's degree in pharmacy or a relevant Science Degree with at least 5 years working experience.
• The incumbent musthave a working knowledge of c
• GMP.
• Experience in health products manufacturing or regulation environment will be an added advantage.have the ability to pay attention to detail, prioritize work and handle multiple assignmentsdemonstrate management ability and leadership, and potential to drive technical quality strategy implementation.
• Previous management experience will be a distinct advantage.have excellent verbal and written communication skills.
• Experience in conducting training will be a distinct advantage.

How to Apply

Interested candidates who meet the above requirements are invited to submit their CVs , certified certificates and reference letters by 10th July 2026 to: te••••••@••••••.bw