Letap Pharmaceuticals Limited, Accra is seeking to recruit personnel in the area of Quality Control Operation.

Reports to: Quality Control Manager

Under the strict guidance of the Quality Control Manager, qualified applicant will be responsible for the following:

•  Develops and validates all analytical methods for the control of raw materials, semi-finished products (in-process blend) and finished products
•  Ensures routine maintenance of quality control data to support testing results by demonstrating that measurement processes are maintained in statistical control
•  Prepares specifications for raw materials, intermediates, semi-finished products and/or products used in pharmaceutical preparations
•  Performs routine analytical testing on API's and FDFs as establishment of SOPs for chemical evaluation of diverse samples
•  Maintains technical understanding of the principles of various analytical techniques, instrumentation, and supporting computer applications
•  Performs on-going stability testing of all pharmaceutical products and submit stability report
•  Develops products performance chart for inclusion in the QA annual product quality review report
•  Supervises the receipt of incoming raw materials in the warehouse
•  Tests and releases all products packaging materials
•  Ensures timely closure of QC documentations in Batch Manufacturing Records (Batch Cards)
•  Responsible for annual performance verification of high performance liquid chromatographs in QC

Qualification Required & Experience

•  Bachelor's Degree in Chemistry, Biological Sciences, Biochemistry etc. Master's Degree in any of these areas (Analytical Chemistry, Pharmaceutical Quality Assurance Pharmaceutical Analysis & Quality Control) may be an advantage
•  Not less than three (3) years of working experience in Pharmaceuticals Quality Control testing

Technical Skills & Attributes:

Ability to work under intense pressure, Self reliant, Smart, Flexible, Team player, Sound knowledge in Microsoft office, Knowledge in GLP, cGMP, Conversant with ICH guidelines for finished product stability studies and USP/ICH method validation guidelines, Very strong practical experience in cleaning validation of production equipment

How To Apply For The Job

Submit Application to:

Letap Pharmaceuticals Ltd
P. O. Box GP 3346
Accra-Ghana

Closing Date:  12 November, 2012