Sr. Executive

2 weeks ago

Jeddah, Makkah Province, Saudi Arabia Jamjoom Pharma Full time

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region.

The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions.

Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.


Role Summary:


To perform sampling of pharmaceutical Raw materials (API & Excipient) as per SOP and guidelines provided under the established environmental condition.

The samples to be submitted to QC lab as required for testing.

Responsibilities:

  • To perform sampling of Raw Material as per schedule and Lead time.
  • To use the SAP, ERP System for the sampling of Raw Materials
  • To perform identification test of required samples on NIR.
  • Maintenance & Daily checks of Analytical Balance and humidity /temperature records of dispensing booths
  • To observe, record and inform any deviation during sampling of Raw Materials.
  • To inform any discrepancies /damages observe during sampling to the supervisor.
  • To maintain sampling tools as per procedure.
- cGMP and GLP Compliance in sampling area. Maintain good documentation practice.

  • Analysis of all types of raw materials including APIs and Excipients.
  • To obtain training on various techniques used for Raw Material analysis.
  • To learn advanced analytical techniques and operation of analytical instruments.
  • Maintenance & Daily checks of Analytical Balance, pH Meters
- cGMP / GLP Compliance in QC Laboratory. Maintain good documentation practices.

  • To maintain the reference standards, chemicals, reagents, Volumetric Solutions and solvents list and report to the supervisor.
  • To maintain logbooks and record of all lab activities.
  • Perform test method transfers in compliance with relevant pharmacopeia, existing SOP / Protocol & cGMP.
  • To perform the calibration of the laboratory instruments as per schedule.
  • Preparation of secondary reference standards.
  • Sample receiving, Sample quantity deduction and Entry of ATR in logbook.
  • To perform different functions authorized in quality module of SAP

Qualifications:

  • Bachelor's or Master's degree in Chemistry or B. Pharm.
  • 3 to 6 years' experience in Pharmaceuticals Quality Control
  • Knowledge of using computer. MS Excell and MS words
  • Working with Business process software such as ERP-SAP
  • Knowledge of Pharmaceutical Quality control and GMP/ GLP values

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