Pharma QC Analyst: Lab Precision & Compliance

Tanqeeb; Abu Dhabi; On-site; AED 90,000 - 150,000; Full time

Job summary

Tanqeeb is seeking a Pharmaceutical Quality Control Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in accordance with approved methods and GMP/GLP standards.

The role requires 3–6 years in pharmaceutical QC, hands-on expertise with HPLC, GC, UV-Vis, and dissolution testing, and strong data integrity skills. You will document results, support QMS activities, and collaborate with QA, Production and R&D.

Qualifications

• Bachelor’s degree in Pharmacy or Chemistry or related Science.
• 3–6 years pharmaceutical Quality Control experience.
• Hands-on experience with HPLC, GC, UV-Vis spectrophotometry and dissolution testing.
• Solid knowledge of GMP, GLP, SOPs and regulatory guidelines (USP/EP/BP).
• Experience in analytical method validation and method transfer.
• Strong data integrity and ALCOA+ compliance.

Responsibilities

• Perform chemical and physical analysis of raw materials, finished products, and stability samples.
• Operate QC lab equipment (HPLC, GC, UV-Vis, dissolution testers, etc.).
• Ensure testing is accurate, timely, and compliant with GMP/GLP and regulatory standards.
• Maintain records in line with GDP and Good Documentation Practices.
• Enter results into SAP accurately and on time.
• Support QMS activities including CAPA, AMS, Change Controls.

Skills

HPLC

GC

UV-Vis spectrophotometry

Dissolution testing

GMP/GLP knowledge

SOP adherence

Data integrity ALCOA+

Analytical method validation

Method transfer

SAP

AmpleLogic

Cross-functional collaboration

Education

Bachelor’s degree in Pharmacy or Chemistry

Tools

SAP

AmpleLogic

Job description

Tanqeeb is seeking a Pharmaceutical Quality Control Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in accordance with approved methods and GMP/GLP standards.

The role requires 3–6 years in pharmaceutical QC, hands-on expertise with HPLC, GC, UV-Vis, and dissolution testing, and strong data integrity skills. You will document results, support QMS activities, and collaborate with QA, Production and R&D.