Key responsibilities:
Analyse samples of raw materials and finished pharmaceutical products to determine quality against set standards
Compile and record data for documentation required for preparation of certificates of analysis
Maintain inventory of laboratory reagents, chemicals, glassware for accountability
Review and update standard operating procedures related to the quality control laboratory.
Ensure compliance to safety and regulatory requirements while working under Good Laboratory Practices (GLP).
Manage equipment including performing calibration and basic maintenance as required.
Maintain records for consumables e.g HPLC columns, reference standards and reagents during sample analysis.
Maintain general cleanliness of the quality control laboratory.
Job requirements:
Bachelor’s Degree in Analytical Chemistry or any other related course
At least 5 years experience in a pharmaceutical laboratory
If you fit this profile, kindly email your written application and CV to hr@meds.or.ke
Apply via :
hr@meds.or.ke
