QC Lab Specialist — Pharma QA & Audits

Olayancareer; Dammam; On-site; SAR 60,000 - 100,000; Full time

Job summary

Olayancareer in Saudi Arabia is seeking a QC Analyst to support testing and documentation across manufacturing stages in the pharmaceutical sector. The role requires a Bachelor degree in Chemistry or Chemical Engineering and at least two years of relevant industry experience.

You will perform tests per approved procedures, troubleshoot instruments, support audits, maintain Good Documentation Practice, and assist with SOP updates and inventory management within a compliant lab environment.

Qualifications

• Bachelor degree in Chemistry, Chemical Engineering or equivalent.
• Two years or more relevant experience in Pharmaceuticals or related industries.

Responsibilities

• QC Analysts prepare, sample, and test samples from all phases of manufacturing or handling processes.
• Prepare documentation/technical reports for tests performed and any adverse events.
• Perform tests according to approved testing procedures.
• May also perform instrument troubleshooting, calibration and repair whenever required.
• Able to handle QC instruments and troubleshoot properly.
• Support in Local and external Audit Programs.
• Pass all internal and external audit without major observation related to human factors.
• Collaborate in the qualification protocols and preparation of SOPs and associated changes to procedures.
• Good documentation practice.
• Assist supervisor in the out of limit (OOL) investigation.
• OOL investigation completion.
• Perform inventory and requests for lab reagents and consumables.

Education

Bachelor degree of Chemistry, Chemical Engineering or equivalent

Job description

Olayancareer in Saudi Arabia is seeking a QC Analyst to support testing and documentation across manufacturing stages in the pharmaceutical sector. The role requires a Bachelor degree in Chemistry or Chemical Engineering and at least two years of relevant industry experience.

You will perform tests per approved procedures, troubleshoot instruments, support audits, maintain Good Documentation Practice, and assist with SOP updates and inventory management within a compliant lab environment.