Senior Validation & Compliance Leader

Julphar

United Arab Emirates

On-site

AED 500,000 - 700,000

Full time

8 days ago

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Job summary

Julphar, a leading pharmaceutical company in the United Arab Emirates, seeks a seasoned professional to lead qualification and validation activities across equipment, utilities, and computerized systems. The role emphasizes GMP/GDP compliance, data integrity, and regulatory readiness, including FDA/WHO/EU guidelines, with a focus on risk-based approaches and continuous improvement.

The candidate will manage qualification lifecycle, calibrations, audits, and cross-functional coordination within a

Qualifications

  • Bachelor’s degree in Engineering, Science, or Pharmacy.
  • 10+ years in equipment/utility qualification, calibration, and validation in pharma.
  • Strong GMP, GDP, ISO 9001, ISO 14001 knowledge.
  • Experience with FDA, WHO, and EU guidelines.
  • CSV experience and calibration systems.
  • Leadership of technical teams and cross-functional projects.
  • Proficiency in data integrity (ALCOA+) and regulatory inspections.

Responsibilities

  • Lead end-to-end qualification lifecycle of equipment, facilities, and utilities.
  • Oversee qualification of critical utilities and cleanrooms per ISO 14644.
  • Lead validation of computerized systems (CSV) and ensure regulatory compliance.
  • Manage calibration activities and deviation resolution.
  • Provide technical guidance and supervise Validation SMEs.
  • Support change controls, CAPA, and audits via EQMS.
  • Coordinate cross-functional activities and documentation management.
  • Drive continuous improvement and risk management initiatives.

Skills

Leadership & people management
Quality systems
Validation & qualification
Regulatory compliance

Education

Bachelor's degree in Engineering, Science, or Pharmacy

Tools

EQMS
Microsoft Office

Job description

Julphar, a leading pharmaceutical company in the United Arab Emirates, seeks a seasoned professional to lead qualification and validation activities across equipment, utilities, and computerized systems. The role emphasizes GMP/GDP compliance, data integrity, and regulatory readiness, including FDA/WHO/EU guidelines, with a focus on risk-based approaches and continuous improvement.

The candidate will manage qualification lifecycle, calibrations, audits, and cross-functional coordination within a

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