• Quality Compliance: Monitor and ensure compliance with all relevant regulations, guidelines, and industry standards for pharmaceutical manufacturing and quality control. • Documentation Management: Maintain accurate and organized documentation related to quality control processes, including batch records, standard operating procedures (SOPs), and quality testing data. • Batch Release: Review batch records and associated documentation to ensure that products meet quality specifications before release for distribution. • Quality Audits: Participate in internal and external quality audits to assess compliance with regulatory requirements and identify areas for improvement. • CAPA Management: Contribute to the identification and implementation of Corrective and Preventive Actions (CAPA) in response to quality issues, deviations, and non-conformances. • Root cause and investigation: Identify the gaps or deviations in the system and follow up to ensure that they are resolved. • Change Control: Review and assess proposed changes to processes, equipment, or procedures to determine their potential impact on product quality and compliance. • Supplier Quality: Collaborate with suppliers and vendors to evaluate their quality systems and ensure the quality of incoming raw materials and components. • Quality Training: Assist in the development and delivery of quality-related training programs for employees to enhance their understanding of quality principles and practices. • Product Complaints: Investigate and analyze customer complaints related to product quality and work with relevant departments to implement corrective actions. • Validation Activities: Support validation activities, including equipment qualification, process validation, and cleaning validation, to ensure that processes are capable of consistently producing quality products. • Risk Assessment: Participate in risk assessment activities to identify potential quality risks and develop strategies to mitigate them. • Continuous Improvement: Contribute to the continuous improvement of quality systems by identifying opportunities for streamlining processes and enhancing efficiency.

• Bachelor’s degree in Medical/Pharmacy/Biomedical Engineering or related fields. • Strong information retrieval and data analysis skills, as well as excellent official document writing abilities； • Strong resilience, ability to face challenges and adapt to new things. • Previous experience (3+ years) in quality assurance within the pharmaceutical or related industry. • Familiarity with pharmaceutical regulations and guidelines, such as Good Manufacturing Practices (GMP) and International Council for Harmonisation (ICH) guidelines. • Strong attention to detail and analytical skills to assess quality data and trends. • Experience with quality management systems and documentation practices. • Problem-solving abilities to address quality issues and implement appropriate solutions. • Knowledge of risk assessment and root cause analysis methodologies. • Certification in Quality Management or Quality Assurance is desirable.

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