Senior QC Specialist — GMP/GLP Analytics

Julphar; United Arab Emirates; On-site; AED 100,000 - 201,000; Full time

Job summary

Julphar in the United Arab Emirates seeks a QC Analyst to ensure GLP and GMP adherence, perform chemical and physical analyses, operate QC instruments, and maintain meticulous records. The role includes data entry in SAP, analytical method validation, and support for audits and CAPAs.

The ideal candidate holds a Bachelor’s degree in pharmacy or science with 3–6 years of relevant experience in a pharma QC environment, and a strong commitment to data integrity and regulatory compliance.

Qualifications

• Bachelor’s degree in pharmacy or science required.
• Experience in GMP/GLP environments is essential.
• Proficient with QA/QC documentation and record-keeping.

Responsibilities

• Ensure GLP, GMP, safety procedures and maintain hygienic lab conditions.
• Carry out chemical and physical analysis of finished/ raw material and stability.
• Operate QC equipment as per section assignment.
• Record all analytical data accurately.
• Enter analysis data into SAP.
• Ensure final products meet specifications and regulatory requirements.
• Adhere to SOPs and assist audits; address observations.
• Manage CAPAs, AMS, and change controls in the quality system.
• Maintain data integrity and good documentation practices in QC labs.
• Support problem solving and troubleshoot day-to-day operations.
• Assist supervisors and delegates in assigned tasks.

Skills

GMP/GLP knowledge

Data integrity

Analytical method validation

Auditing

Documentation & data recording

Cross-functional communication

Troubleshooting

EMS & EHS compliance

Education

Bachelor’s degree in pharmacy/science

Tools

SAP

HPLC

GC

UV-Vis

Job description

Julphar in the United Arab Emirates seeks a QC Analyst to ensure GLP and GMP adherence, perform chemical and physical analyses, operate QC instruments, and maintain meticulous records. The role includes data entry in SAP, analytical method validation, and support for audits and CAPAs.

The ideal candidate holds a Bachelor’s degree in pharmacy or science with 3–6 years of relevant experience in a pharma QC environment, and a strong commitment to data integrity and regulatory compliance.