Junior QC Chemist: GMP/GLP Analysis & Data Integrity

Julphar; United Arab Emirates; In loco; AED 180.000 - 280.000; Tempo pieno

Descrizione del lavoro

Julphar is seeking a Quality Control professional to perform chemical and physical analysis of raw materials, semi-finished products, and stability samples. The role involves operating HPLC, GC, UV-Vis spectrophotometers, and dissolution equipment to ensure results meet GMP/GLP standards.

The candidate will maintain meticulous records, input data into SAP, and support QMS activities including CAPA and Change Controls. Collaboration with QA, Production, and R&D is essential.

Competenze

• Bachelor's degree in Pharmacy, Chemistry, or related science required.
• Minimum 3–6 years of relevant experience in pharmaceutical quality control.
• Strong 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 method validation, method transfer, and assay analysis.
• Good data integrity practices (ALCOA+) and GDP.

Mansioni

• Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples.
• Operate QC laboratory equipment such as HPLC, GC, UV-Vis, dissolution apparatus.
• Ensure testing is accurate and timely, in GMP/GLP compliance.
• Maintain records of results and observations per GDP.
• Enter results into SAP accurately and timely.
• Support QMS activities including CAPA, AMS, and Change Controls via AmpleLogic.
• Participate in internal and external audits and close observations.
• Maintain lab safety and cleanliness; follow SOPs and GMP.

Conoscenze

HPLC

GC

UV-Vis spectrophotometry

Dissolution testing

GMP/GLP compliance

ALCOA+ data integrity

SAP

AmpleLogic

Analytical method validation

Audit readiness

Formazione

Bachelor's degree in Pharmacy, Chemistry, or a related Science discipline

Strumenti

SAP

AmpleLogic

Descrizione del lavoro

Julphar is seeking a Quality Control professional to perform chemical and physical analysis of raw materials, semi-finished products, and stability samples. The role involves operating HPLC, GC, UV-Vis spectrophotometers, and dissolution equipment to ensure results meet GMP/GLP standards.

The candidate will maintain meticulous records, input data into SAP, and support QMS activities including CAPA and Change Controls. Collaboration with QA, Production, and R&D is essential.