Senior QC Specialist: GMP Analytics & Lab Excellence

Julphar; Ras Al Khaimah; Presencial; AED 180.000 - 240.000; Jornada completa

Descripción de la vacante

Julphar is seeking a Senior Specialist – Quality Control (QC) to oversee laboratory operations, analytical testing, and data integrity for finished products and stability studies.

The role requires managing QC instruments (HPLC/GC, UV-Vis, FTIR, AAS, Karl Fischer, dissolution and more), ensuring GMP/GDP compliance, and leading CAPA-driven investigations. A strong background in QC within pharma is essential.

Formación

• Bachelor’s or Master’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a relevant scientific discipline.
• Relevant experience in Quality Control within the pharmaceutical manufacturing industry.
• Experience in pharmaceutical analytical testing, laboratory operations, and analytical data review.
• Practical experience with chromatographic techniques, particularly HPLC and GC, and other relevant QC analytical instruments.
• Experience in stability management, analytical method validation, method transfer, and laboratory investigations.
• Demonstrated experience in supervising, coordinating, or providing technical guidance to QC analysts.
• Experience in GMP‑regulated environments and preparation/review of QC documentation.
• Strong knowledge of pharmaceutical GMP, GLP, GDP, data integrity, and applicable pharmacopoeial standards.
• Proficiency in analytical testing techniques and laboratory instrumentation.
• Strong understanding of OOS, OOT, deviation management, CAPA, root cause analysis, and Quality Risk Management.
• Knowledge of analytical method validation, method transfer, stability studies, and process validation.
• Familiarity with SAP and laboratory documentation systems.
• Knowledge of audit requirements, regulatory compliance, and laboratory safety standards.
• Ability to interpret analytical data and make scientifically sound decisions.
• Strong analytical thinking and scientific problem‑solving capabilities.
• Excellent planning, coordination, and prioritization skills.
• Effective communication and stakeholder management skills.
• Strong people management, coaching, and training capabilities.
• High sense of accountability, ownership, and result orientation.
• Attention to detail, accuracy, and commitment to data integrity.
• Ability to adapt to changing priorities and manage multiple tasks effectively.
• Strong written and verbal communication skills in English.

Responsabilidades

• Oversee QC laboratory operations and analytical testing to ensure timely, compliant results.
• Allocate testing activities to analysts and monitor workload and priorities.
• Ensure products comply with specifications, pharmacopoeial standards, and regulatory requirements.
• Manage instrument calibration and performance monitoring of QC equipment.
• Develop and implement analytical methods per approved specifications and regulatory needs.
• Review HPLC/GC data and ensure accuracy, completeness, and traceability.
• Lead investigations into OOS/OOT and other quality events and implement CAPAs.
• Coordinate stability studies and review related protocols and reports.
• Provide training and mentorship to QC analysts; support onboarding and competency development.
• Support audits, inspections, and readiness activities; ensure safety and GDP compliance.

Educación

Bachelor’s or Master’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences

Herramientas

HPLC

GC

UV-Vis Spectrophotometer

FTIR

AAS

Karl Fischer Titrator

Descripción del empleo

Julphar is seeking a Senior Specialist – Quality Control (QC) to oversee laboratory operations, analytical testing, and data integrity for finished products and stability studies.

The role requires managing QC instruments (HPLC/GC, UV-Vis, FTIR, AAS, Karl Fischer, dissolution and more), ensuring GMP/GDP compliance, and leading CAPA-driven investigations. A strong background in QC within pharma is essential.