QA Specialist - Validation

About the role

EVA Pharma is seeking a motivated QA Specialist – Validation to join its Quality Assurance team at the factory in Hautat Sudair, Riyadh Province. The role ensures validation processes meet regulatory standards and supports product quality.

Key responsibilities

• Execute, review, and approve validation protocols for equipment, systems, and processes.
• Coordinate and perform ongoing validation activities, including risk assessments, change controls, and requalifications.
• Review and approve validation documentation and reports for accuracy and regulatory compliance.
• Maintain and update validation master plans and schedules.
• Provide training and support to personnel on validation requirements and best practices.

Required profile

• Bachelor’s degree in Pharmacy, Engineering, or a related scientific field.
• 1‑3 years of experience in QA or validation within the pharmaceutical or biotechnology industry.
• Strong understanding of validation principles, regulatory guidelines, and SFDA GMP requirements.
• Excellent analytical, problem‑solving, communication, and interpersonal skills.
• Proficiency with validation documentation and related software tools.

Required skills

• SFDA GMP requirements
• Risk assessments
• Validation protocols
• Change controls
• Validation documentation
• Requalifications
• Regulatory compliance