Sr. Executive - Quality Control

Jamjoom Pharma

Jeddah, Makkah
US$30,000-40,000 per year
Permanent
Full-time

2 months ago
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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.To conduct routine and non-routine chemical analysis of Raw Materials, Intermediate/bulk and Finished Products manufactured in Jamjoom Pharma in pharmacopeias and cGMP guidelines and to apply and follow the laid down procedures of the quality management system in Quality Control unit as per guidelines of pharmaceutical industry and to maintain Lab. equipment and instruments as per applicable procedure and to achieve business objectives.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

Jamjoom Pharma