Validation Engineer

AL Alamiya Veterinary Medicines Manufacturer; Al Ain; On-site; AED 120,000 - 200,000; Full time

Job summary

A leading veterinary pharmaceutical firm in Al Ain is seeking a skilled Validation Engineer to manage and lead validation activities. This role involves developing compliance protocols, ensuring proper documentation, and collaborating across departments. Candidates should have a relevant degree and experience in pharmaceutical validation. Strong knowledge of GMP and ISO standards is essential.

Qualifications

• 3–8 years of experience in pharmaceutical, veterinary, or feed manufacturing validation.
• Strong knowledge of GMP, ISO, and international validation guidelines.
• Broad understanding of validation for different production lines.

Responsibilities

• Lead and manage validation activities across various systems.
• Develop and implement the Validation Master Plan.
• Ensure documentation and audit readiness for validations.

Skills

GMP compliance

Validation protocols

Risk assessment

Documentation skills

Communication skills

Education

Bachelor’s degree in Pharmaceutical Engineering

Bachelor’s degree in Chemical Engineering

Bachelor’s degree in Biotechnology

Job description

Al Alamia Vet is a leading veterinary pharmaceutical and feed additive manufacturer in the UAE, committed to high-quality, GMP-compliant products for poultry, ruminants, camels, and equine. We are expanding our operations and seeking a skilled Validation Engineer to join our growing team.

Role & Responsibilities

• Lead and manage all validation activities across equipment, utilities, processes, cleaning, computerized systems, and analytical methods.
• Develop, implement, and update the Validation Master Plan (VMP) for the site.
• Plan, prepare, and execute validation and qualification protocols in compliance with GMP and regulatory requirements.
• Ensure proper documentation, reporting, and audit readiness for all validation activities.
• Conduct risk assessments and propose improvements to maintain compliance and efficiency.
• Collaborate with QA, QC, R&D, Manufacturing, and Engineering to support new projects and ongoing operations.
• Investigate validation-related deviations and oversee CAPA (Corrective and Preventive Actions).
• Provide training and guidance to staff on validation practices and standards.

Qualifications

• Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, Biotechnology, or related field.
• 3–8 years of experience in pharmaceutical, veterinary, or feed manufacturing validation.
• Strong knowledge of GMP, ISO, and international validation guidelines (EU / FDA / WHO).
• Broad understanding of equipment, process, cleaning, computer system, and method validation for different production line and other supportive machine.
• Excellent documentation and communication skills.