Senior Validation Executive

Join Jamjoom Pharma as a Senior Validation Executive 

Are you a detail‑obsessed professional with a passion for operational excellence and quality assurance? Jamjoom Pharma is seeking a dynamic Senior Validation Executive to drive precision, compliance, and efficiency in our fast‑paced Quality team. This is your chance to make a measurable impact in one of the region’s leading pharmaceutical companies.

Key Responsibilities

• Ensure all validation activities comply with current Good Manufacturing Practices (cGMP).

• Prepare and maintain the Validation Master Plan and oversee the full validation lifecycle.

• Collaborate cross‑functionally with Manufacturing, Quality Control, Engineering, and Regulatory Affairs.

• Act as a subject matter expert during regulatory inspections and internal audits.

• Prepare and execute Aseptic Process Simulation (APS) protocols and reports.

• Develop and implement Cleaning Validation protocols aligned with global standards.

• Author and execute validation protocols (IQ/OQ/PQ) for equipment, APS, utilities, manufacturing processes, and cleaning procedures.

• Lead and manage smaller validation projects from initiation to completion.

• Analyze validation data, identify discrepancies, and prepare comprehensive summary reports.

• Investigate and resolve validation deviations and non‑conformances.

• Collect, review, and verify complete documentation for validation processes.

• Prepare Process Validation files for export markets, including CTD and eCTD formats.

• Lead Performance Qualification (PQ) for machines, utilities, and production equipment.

• Prepare Computerized System Validation (CSV) protocols and reports to support data integrity and system compliance.

• Drive validation strategy in collaboration with QA, Production, Engineering, and RA teams.

What We’re Looking For

• Proven experience in pharmaceutical validation.

• Strong knowledge of international regulatory frameworks (ICH, WHO, FDA, EMA, GMP).

• Detail‑oriented, organized, and proactive leadership style.

• Excellent documentation, communication, and analytical skills.

• Strong problem‑solving abilities and a collaborative team spirit.

Qualifications & Experience

• Bachelor’s degree in pharmacy.

• Minimum 6+ years of hands‑on experience in Validation and Qualification within the pharmaceutical industry.

• Proven experience preparing CTD/eCTD dossiers for international markets.

• Hands‑on execution of validation protocols including Equipment Qualification, CSV, Media Fill, Cleaning Validation, and Utilities Qualification.

• Deep understanding of cGMP, FDA 21 CFR Part 211, EU Annex 15, and other relevant guidelines.

• Ability to manage multiple priorities in a dynamic environment.