Quality Control jobs in Saudi Arabia
Quality Control Inspector
Packers Plus Energy Services Inc
Discover more opportunities than anywhere else. Find more jobs nowSenior Quality Control Officer
Tabuk Pharmaceuticals
Connect with headhunters to apply for similar jobsHead of Quality Assurance – Medical Devices | Saudi Arabia
RAWAJ
Head of Quality Assurance – Medical Devices | Saudi Arabia
Rawaj HCM Jobs
Senior Health & Safety Coordinator (Saudi National) - Night Shift
Parsons Oman
Executive - Quality Control
Job summary
A leading pharmaceutical company in Jeddah is seeking a professional to conduct routine and non-routine chemical analysis of products. The ideal candidate will have a Bachelor’s or Master’s in Chemistry and 3-5 years of experience in Pharmaceuticals Quality Control. Responsibilities include ensuring compliance with specifications and providing training on analytical techniques. Knowledge of cGMP and SFDA regulations is required.
Qualifications
- 3 to 5 years' experience in Pharmaceuticals Quality Control.
- Familiar with cGMP and SFDA regulatory compliance.
Responsibilities
- Conduct routine and non-routine chemical analysis of products.
- Perform testing of market complaint samples whenever required.
- Provide training to trainees on analytical techniques.
Skills
Education
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 (SOPs). To perform routine and Critical Tests in Finished goods samples. To qualify Raw material as Secondary Reference Standards as per protocol.
- 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.
- 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.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.