Number of Positions Available: 10

Department: Quality Control

Reports To: QC manager

Employment Type: Full-Time

• Application Deadline: 1st June, 2026.

• Only shortlisted candidates will be contacted.

• For inquiries, contact HR on +256 707850054.

Required Qualifications & Experience

• Diploma Science technology chemistry from a recognised institution or a related scientific discipline.
• Minimum of 0–above years’ experience in pharmaceutical quality control and Quality assurance or a GMP-regulated laboratory environment.
• Knowledge on HPLC, UV-Vis, FTIR, dissolution testers, Karl Fischer titrators, and analytical balances.
• Sound knowledge of GMP, GLP, ICH guidelines, and pharmacopeial requirements (USP, BP, EP).
• Proven experience in analytical method validation, impurity profiling, and stability studies.
• Experience in documentation control, SOP writing, and regulatory compliance.

Key Competencies & Attributes

• High level of integrity, accuracy, and attention to detail
• Strong analytical and problem-solving skills
• Ability to work independently with minimal supervision
• Excellent teamwork, communication, and mentoring skills
• Strong organizational and documentation skills
• Commitment to continuous professional development and quality improvement

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