QC Specialist – GMP/GLP Lab & Data Integrity

Tanqeeb; Abu Dhabi; On-site; AED 180,000 - 240,000; Full time

Job summary

Julphar in Abu Dhabi invites a QC Analyst to join our pharmaceutical quality control team. You will perform chemical and physical analyses of finished/ raw materials, operate QC equipment, and record data in SAP, ensuring product compliance with GMP/GLP and regulatory standards.

The role requires a Bachelor’s degree in pharmacy or science and 3–6 years of relevant experience, with strong attention to detail and data integrity. Proficiency in HPLC, GC, and UV-Vis is preferred.

Qualifications

• Bachelor’s degree in pharmacy or science.
• Proficient with computer software applications.
• Minimum 3–6 years’ experience in QC/analytical labs.
• Familiar with GMP/GLP guidelines.

Responsibilities

• Ensure GLP, GMP and safety procedures in lab.
• Carry out chemical and physical analyses of finished/ raw materials.
• Operate QC equipment and record data.
• Enter analysis data in SAP.
• Ensure final products meet specifications and regulations.
• Support audits and close audit observations.
• Maintain data integrity and document control.

Skills

HPLC

GC

UV-Vis

Data integrity

GMP/GLP

ALCOA+

Method validation

Education

Bachelor’s degree in pharmacy/science

Tools

SAP

Job description

Julphar in Abu Dhabi invites a QC Analyst to join our pharmaceutical quality control team. You will perform chemical and physical analyses of finished/ raw materials, operate QC equipment, and record data in SAP, ensuring product compliance with GMP/GLP and regulatory standards.

The role requires a Bachelor’s degree in pharmacy or science and 3–6 years of relevant experience, with strong attention to detail and data integrity. Proficiency in HPLC, GC, and UV-Vis is preferred.