This role provides an opportunity to introduce professionals to the field, provide hands-on experience and develop the necessary skills for quality assurance and control in an IVD manufacturing environment.
Duties and Responsibilities:
- Assist in in-process inspection during test kit manufacturing.
- Support accurate and timely documentation of batch records, deviations, and quality logs.
- Ensure adherence to GMP, ISO 13485:2016, and internal quality standards.
- Participate in line clearance, sampling, and non-conformance reporting.
- Supporting equipment and facility qualification activities.
- Contribute to continuous improvement in quality control processes.
Who We’re Looking For:
Bachelor’s degree in:
• Industrial Chemistry
• Pharmacy
• Biomedical Sciences
• Biological Sciences
• Quality Management
• Any related science or technical discipline
What you need to succeed in this role:
Strong interest in quality systems, medical device manufacturing, and documentation
Basic understanding of ISO 13485, ISO 9001 and cGMP is an added advantage
Excellent observation and reporting skills
Willingness to learn and grow in a fast-paced, regulated environment
All eligible applicants should submit their applications with detailed and up to date CVs, copies of academic transcripts and certificates and any other supporting documents, day time telephone contacts or email to:
The Director Human Resource,
Microhaem Scientifics and Medical Supplies Limited
Plot 16 A-C Martyrs Way Ntinda
P.O Box 73496, Kampala, Uganda
Applications should be sent by email to: recruitment@microhaem.co.ug as a single file in Portable Document Format (PDF) not later thanFriday, 23rd May 2025 by 5:00pm.
Please note that only shortlisted applicants will be contacted.
