Executive - Quality Control

Jamjoom Pharma; Jeddah; On-site; SAR 120,000 - 150,000; Full time

Job summary

A leading pharmaceutical company in Saudi Arabia is seeking a Quality Control Analyst to conduct chemical analyses and ensure compliance with established specifications. The ideal candidate will have a degree in Chemistry and 3 to 5 years of experience in pharmaceuticals quality control. Responsibilities include analysis of finished products and maintenance of compliance with regulatory standards.

Qualifications

• 3 to 5 years’ experience in Pharmaceuticals Quality Control.
• Familiarized with cGMP and SFDA regulatory compliance.

Responsibilities

• Conduct routine and non-routine chemical analysis.
• Analyze finished products with emphasis on first pass analysis.
• Maintain documentation practices and compliance.

Skills

Data analysis

Good observation capabilities

Fire safety awareness

Knowledge of pharmaceutical products

Education

Bachelor’s or Master’s degree in Chemistry

Job description

Overview

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 conduct routine and non-routine chemical analysis of bulk, intermediate and finished products and to ensure its compliance with specification and to ascertain that analysis is completed according to established Standard Operating Procedures (SOP’s). To perform routine and Critical Tests in Finished goods samples. To qualify Raw material as Secondary Reference Standards as per protocol.

Responsibilities

• Analysis of Finish Products as per the schedule with emphasis on first pass analysis.
• Inventory of Lab requirements including Glassware/ Stationary.
• Work in another department whenever required like AMD (due to unavailability of instrument in QC).
• To provide training to trainee's on the analytical techniques used for the Finish Goods analysis.
• To learn incorporation of data and other functions related to SAP.
• cGMP / GLP Compliance in QC Laboratory. Maintain good documentation practices.
• To maintain reference standards, chemicals, reagents, and solvents.
• Raise OOS and fill LIR in given time Frame.
• Perform testing of market complaint samples whenever required.
• To look for logbooks for proper entries.
• Maintenance & Daily checks of Analytical Balance, pH Meters.
• Support in procurement procedure related to instruments/Reagents/Standards.
• To prepare User requirement for the CAPEX approved instruments.
• Carryout Analytical Method transfer between the two labs.

Qualifications

• Bachelor’s or Master’s degree in Chemistry.
• 3 to 5 years’ experience in Pharmaceuticals Quality Control.
• Basic fire safety Awareness.
• Knowledge of Pharmaceutical products.
• Data analysis and good observation capabilities.
• Familiarized with cGMP and SFDA regulatory compliance.