Letap Pharmaceutical Limited Careers

Posted on :

1 Nov, 2011

Category :

Research Jobs in Ghana

Analytical Research & Development/Quality Control Officer

Letap Pharmaceutical Limited, Accra is seeking to recruit personnel in the areas of Analytical Research and Development, and Quality Control Operations.

Reports to: Research and Development Manager

Under the guidance of the R&D Manager, qualified applicant will be responsible for the following:

  • Development of specifications and analytical test procedures for raw materials, in-process, finished products and packaging materials
  • Responsible for development of stability indicating analytical test procedures, validation and/or verification of analytical procedures as per regulatory requirements
  • Assists in the development of stability protocols for newly developed products and executes stability studies (stress, in-use, on-going, real and accelerated) on finished products
  • Control of all Research and Development documents
  • Assists in the compilation of product dossiers (CTD formal) for regulatory submission
  • Engineers the transfer of all verified and/or validated test procedures from R&D to Quality Control
  • Identifies gaps in QC functions and helps build them appropriately for quality systems improvements
  • Assists in training of QC functions and helps build them appropriately for quality systems improvements
  • Assists in training of QC Analysts/Chemists on new analytical methodologies
  • Involves in preparations of analytical and production equipment qualifications documents

 

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Required Skills or Experience

  • Bachelors Degree in Chemistry, Biological Sciences, Biochemistry etc. Masters Degree in any of these areas (Analytical Chemistry, Pharmaceutical Analysis & Quality Control) may be an advantage
  • Not less than two years of working experience in Pharmaceutical Quality Control

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 products stability studies and USP/ICH method validation guidelines, very strong practical experience in cleaning validation of production equipment

 

How To Apply

Submit Application to:


Letap Pharmaceuticals Ltd
P. O. Box 3346
Accra – Ghana
Closing 01 Dec, 2011


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