• Leadership and Team Management • Lead and mentor a team of engineers to support operational goals and maintain cGMP compliance. • Foster a collaborative work environment that emphasizes teamwork, accountability, and technical excellence. • Evaluate team performance, provide constructive feedback, and develop training programs to upskill staff. • Process Improvement and Optimization • Analyze current production processes to identify bottlenecks, inefficiencies, and areas for improvement. • Lead efforts to implement lean manufacturing principles and continuous improvement methodologies. • Ensure that equipment and processes are optimized to increase throughput, reduce costs, and maintain high product quality. • Equipment and Facility Management • Oversee the installation, maintenance, and calibration of equipment in compliance with cGMP standards and regulatory requirements. • Develop and manage a preventive maintenance schedule to maximize equipment uptime and minimize unexpected downtime. • Lead troubleshooting efforts and coordinate corrective actions for equipment and facility-related issues. • Project Management • Manage capital projects related to equipment upgrades, process improvements, and facility expansions from concept to completion. • Develop project scopes, budgets, and timelines, and ensure all projects are completed on time, within budget, and in compliance with regulatory standards. • Collaborate with cross-functional teams to ensure project alignment with overall operational objectives. • Compliance and Documentation • Ensure compliance with all relevant regulations, including cGMP, NDA, and ISO standards, through rigorous documentation and record-keeping. • Work closely with the quality assurance team to conduct audits, investigations, and root cause analyses for any deviations or non-conformances. • Implement effective change control processes to manage modifications to processes, equipment, or facility layout. • Environmental Health and Safety (EHS) Standards • Develop and enforce Environmental Health and Safety procedures to ensure a safe working environment for all employees. • Conduct risk assessments and implement mitigation measures to reduce potential hazards. • Ensure compliance with EHS regulations and lead initiatives to continuously improve safety performance. • Vendor and Stakeholder Management • Manage relationships with equipment suppliers, service providers, and contractors to ensure high-quality service and support. • Collaborate with internal stakeholders, including quality, regulatory, supply chain, and production teams, to ensure seamless operations. • Support quality audits and inspections by regulatory authorities, addressing any engineering-related questions or findings.

• Minimum Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related field) Master’s degree is an added advantage. • Minimum of 5 years of engineering experience in a cGMP-regulated environment, with at least 3-5 years in a managerial or supervisory role in pharmaceutical, biotechnology, or diagnostic kit manufacturing. • Project Management Professional (PMP) and cGMP training are desirable. • Technical Knowledge: Strong understanding of cGMP requirements, NDA regulations, and ISO standards in a manufacturing environment. • Leadership and Communication: Proven leadership skills with the ability to effectively communicate and collaborate across departments and with external stakeholders. • Problem-Solving: Proficiency in troubleshooting complex issues and implementing effective corrective actions. • Analytical Skills: Data-driven mindset with experience in using statistical and analytical tools to monitor process performance and drive improvements. • Project Management: Strong organizational and project management skills with a track record of managing complex engineering projects from start to finish. • HSE Awareness: In-depth knowledge of health, safety, and environmental regulations and best practices in a manufacturing setting.

Send the following requirements to recruitment@microhaem.co.ug -Application letter -CV/Resume with at least 3 referees -Academic documents