QA Specialist - Validation

Eva Pharma; Saudi Arabia; On-site; SAR 200,000 - 300,000; Full time

Job summary

A leading pharmaceutical company in Riyadh Province, Saudi Arabia is seeking a skilled QA Specialist – Validation. This role involves executing and approving validation protocols, maintaining documentation, and ensuring compliance with regulatory guidelines. The ideal candidate will have a degree in Pharmacy or Engineering and 1-3 years of experience in QA or validation. Joining us means becoming part of a supportive team dedicated to health and well-being. Competitive compensation and training opportunities are offered.

Qualifications

• 1-3 years of experience in QA or validation within the pharmaceutical or biotechnology industry.
• Strong understanding of validation principles and regulatory guidelines.
• Familiarity with SFDA GMP requirements.

Responsibilities

• Execute, review, and approve validation protocols for compliance.
• Coordinate ongoing validation activities and risk assessments.
• Review and approve validation documentation and reports.
• Maintain and update validation master plans and schedules.
• Provide training and support regarding validation practices.

Skills

Analytical skills

Problem-solving skills

Communication skills

Interpersonal skills

Proficiency with validation documentation

Education

Bachelor's degree in Pharmacy, Engineering, or relevant scientific field

Tools

Validation software

Job description

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well‑being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

We are seeking a skilled and motivated QA Specialist – Validation to join our dynamic Quality Assurance team at EVA Pharma's factory in Hautat Sudair, Riyadh Province, Saudi Arabia.

The ideal candidate will ensure the compliance of validation processes and systems, playing a critical role in upholding our commitment to product quality and regulatory compliance.

Key Responsibilities

• Execute, review, and approve validation protocols for equipment, systems, and processes in compliance with industry regulations and internal standards.
• Coordinate and perform ongoing validation activities, including risk assessments, change controls, and requalifications.
• Review and approve validation documentation and reports, ensuring accuracy and compliance with regulatory requirements and internal policies.
• Maintain and update validation master plans and schedules to reflect current practices and regulatory expectations.
• Provide training and support to personnel regarding validation requirements and practices.

Qualifications

• Bachelor's degree in Pharmacy, Engineering, or a relevant 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 and problem‑solving skills.
• Effective communication and interpersonal skills to interact across various departments.
• Proficiency with validation documentation and software.