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Hikma Pharmaceuticals

Methodology Validation Analyst – Contingent Worker

Hikma Pharmaceuticals

Methodology Validation Analyst at Hikma Pharma responsible for analytical validation and quality control analysis. Performing chemical and physical analysis of drug products in compliance with GMP standards.

Posted 6/21/2026full-timeGiza • 🇪🇬 EgyptMid-LevelSeniorWebsite

About the role

Key responsibilities & impact
  • Performing analytical method Validation for Cleaning.
  • Performing analytical method Validation for products and method development.
  • Performing analysis of bulk, semi-finished and finished drug product, if required.
  • Chemical and Physical analysis of HIKMA PHARMA and licensors drug product according to the applicable analytical procedure and after having the necessary training.
  • Performing instrumental analysis using HPLC, UPLC, Gas chromatographs, UV-Vis spectrophotometer, ICP, IR- spectrophotometers and Atomic absorption spectrometer and other minor analytical equipment after having the necessary training).
  • Performing comparative dissolution.
  • Performing Method transfer between R&D and QC departments.
  • Ensures that all obtained results are within the specified approved limit, using a valid method of analysis.
  • Immediate reporting of out of specification test results and preparing deviation reports.
  • Perform Verification for method validation and performing samples for specific analysis in a specific matrix and making validation for test method.
  • Documentation and reporting the analytical results according to the predetermined procedures.
  • Preparation of chemical reagents and other required volumetric solution as directed.

Requirements

What you’ll need
  • Bachelor’s degree in pharmacy with grade Very good.
  • Minimum Experience: 2-3 years of experience in the same position.
  • Ability to work with a team and being an effective team member.
  • Fluency in English, both written and verbal.

Benefits

Comp & perks
  • Complying with the occupational safety and waste procedures in Hikma Pharma plant.
  • Complying with the applicable GMP standards and procedures after having the necessary training.
  • Documentation of analytical results according to the predetermined procedures and reporting events according to the applicable procedures after having the necessary training on the process.

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Hard Skills & Tools
analytical method validationmethod developmentchemical analysisphysical analysisinstrumental analysisHPLCUPLCgas chromatographyUV-Vis spectrophotometryICP
Soft Skills
teamworkeffective communication
Certifications
Bachelor’s degree in pharmacy