Junior Pharma QC Specialist – HPLC/GC Focus

Julphar; Ras Al Khaimah; On-site; AED 90,000 - 150,000; Full time

Job summary

Julphar is seeking a Quality Control Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in accordance with GMP, GLP, and SOPs. You will operate QC instruments (HPLC, GC, UV-Vis, dissolution), maintain lab documentation, and ensure data integrity.

You will enter results into SAP, support QMS activities (CAPA, AMS, Change Controls), participate in audits, and help continuous improvement while maintaining safety and quality standards.

Qualifications

• Perform chemical and physical analysis of raw materials, intermediates, and stability samples per SOPs and GMP/GLP.
• Maintain accurate laboratory records and data integrity according to GDP.
• Operate QC instruments and ensure timely testing and availability of results.

Responsibilities

• Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in accordance with approved analytical methods, specifications, and SOPs.
• Operate QC laboratory equipment, including HPLC, GC, UV-Vis spectrophotometers, dissolution apparatus, and other analytical instruments.
• Ensure all analytical testing activities are performed accurately and within established timelines, in compliance with GMP, GLP, and regulatory requirements.
• Enter analytical results and relevant laboratory data into SAP accurately and on time.
• Support analytical method validation and method transfer activities as required.
• Participate in internal and external audits, provide required laboratory documentation, and support timely closure of audit observations.

Skills

HPLC

GC

UV-Vis

Dissolution

GMP/GLP

SOPs

ALCOA+

Data integrity

SAP

AmpleLogic

Education

Bachelor's degree in Pharmacy

Bachelor's degree in Chemistry

Tools

SAP

AmpleLogic

Job description

Julphar is seeking a Quality Control Analyst to perform chemical and physical analysis of raw materials, intermediates, and stability samples in accordance with GMP, GLP, and SOPs. You will operate QC instruments (HPLC, GC, UV-Vis, dissolution), maintain lab documentation, and ensure data integrity.

You will enter results into SAP, support QMS activities (CAPA, AMS, Change Controls), participate in audits, and help continuous improvement while maintaining safety and quality standards.