Pharma QC Analyst – Analytical Chemist

Julphar; Ras Al Khaimah; On-site; AED 70,000 - 100,000; Full time

Job summary

Julphar is looking for a QC Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in line with GMP, GLP, and internal SOPs.

You will operate HPLC, GC, UV-Vis spectrophotometry, and dissolution equipment, maintain records in GDP, and support QMS activities including CAPA, AMS, and change controls; collaborate with QA, Production, and R&D to ensure regulatory compliance.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry or related science.
• 3–6 years of pharma QC experience.
• Hands-on with HPLC, GC, UV-Vis, and dissolution testing.
• GMP, GLP, SOPs, USP/EP/BP guidelines knowledge.
• Experience in method validation and transfer.
• Data integrity and ALCOA+ compliance.
• SAP and AmpleLogic familiarity.

Responsibilities

• Perform chemical and physical analysis of materials per SOPs and specs.
• Operate QC equipment including HPLC, GC, UV-Vis and dissolution devices.
• Ensure analyses are accurate and timely while complying with GMP/GLP.
• Maintain complete records under GDP and regulatory standards.
• Support QMS activities: CAPA, AMS, Change Controls.

Skills

Analytical testing

GMP/GLP knowledge

Documentation practices

Auditing & CAPA

Team collaboration

Troubleshooting

Time management

Attention to detail

Verbal/written communication

Education

Bachelor's degree in Pharmacy, Chemistry, or related science

Tools

HPLC

GC

UV-Vis spectrophotometry

Dissolution testing

SAP

AmpleLogic

Job description

Julphar is looking for a QC Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in line with GMP, GLP, and internal SOPs.

You will operate HPLC, GC, UV-Vis spectrophotometry, and dissolution equipment, maintain records in GDP, and support QMS activities including CAPA, AMS, and change controls; collaborate with QA, Production, and R&D to ensure regulatory compliance.