Job Details
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Job Description
- Analyzes & tests bulk product intermediates and finished products, in addition, to perform analytical method transfer bulk and re-testing according to the approved protocols and specifications independently.
- Responsible for close supervision of all routine analysis steps done by Q.C. senior and junior analysts and highlighting any deviations noticed to the QC Assistant Manager.
- Performs, supervises and maintains GLP, safety regulations and high standards of lab. performance and housekeeping.
- Prepares, standardizes and maintains availability of reference standards, volumetric solutions, glassware, reagents and ensures their good handling and storage according to the approved SOPs.
- Assist in B.A.R. for products and SOPs. of different section function.
- Receiving of New Product specifications and the Validated Method of analysis from the R&D department.
- Achieving of export requirements concerning finished good section, coordinating with raw and packing section.
- Determining lab requirement (chemicals, instrumental or accessories), and following up purchasing orders.
- Recording after receiving the product samples (Bulk or Finished) from the QA officer and re-delivers it to the senior or junior analysts to be tested.
- Monitoring the laboratory log books (Analyst, Samples & Instruments).
- Changing the status of the bulk product on the ORACLE system from “Quarantine” to “Released” under supervision of the QC Assistant Manager.
Job Requirements
Job Qualification & Requirements :
- General: University graduate, faculty of pharmaceutical sciences or faculty of sciences.
- Technical: At least five years of practical experience in the related job in Pharmaceutical labs:
Knowledge,skills&experience:
- Training courses on instrumental analysis, GLP & safety.
- Excellent knowledge of English language.
- Equipment manipulation and computer skills