The role involves conducting analysis of raw materials and finished products using HPLC equipment in line with regulatory and internal standards. The successful candidate must be able to work independently and follow established laboratory and manufacturing procedures.

Key Responsibilities:

• Operate and maintain HPLC equipment for routine analysis of raw materials and finished pharmaceutical products.
• Document and report analytical results in compliance with Good Laboratory Practices (GLP).
• Support quality control processes by identifying deviations and reporting results accurately.
• Adhere to Good Manufacturing Practices (GMP), GLP, and KEPHIS standards during all laboratory activities.
• Work with minimal supervision and complete assigned tasks within required timelines.
• Collaborate with other departments to ensure product quality and compliance.

Qualifications and Experience:

• Bachelor’s degree in chemistry or a related field.
• Minimum of 5 years’ experience operating HPLC equipment in a pharmaceutical manufacturing setting.
• Knowledge of analytical techniques and procedures in raw material analysis, and finished product analysis
• Experience in Agro-chemical product analysis is an added advantage
• Familiarity with GMP, GLP, and KEPHIS standards.
• Ability to work independently, follow procedures, and maintain accurate records.
• References demonstrating a consistent and reliable work ethic.

Deadline for applications: 30/07/2025