Quality Assurance Specialist

Eva Pharma; Riyad Al Khabra; On-site; SAR 150,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in Saudi Arabia is looking for a Quality Assurance Specialist to ensure compliance with GMP standards and participate in production processes. The ideal candidate should have a Bachelor’s degree in Pharmaceutical Sciences and 0–3 years of relevant experience, with strong knowledge of cGMP regulations and familiarity with quality systems. Experience in Saudi manufacturing is essential.

Qualifications

• 0–3 years of relevant experience in a quality assurance role.
• Familiarity with quality systems such as CAPA and ISO 9001.
• Understanding of validation processes and compliance protocols.

Responsibilities

• Monitor environmental conditions and equipment to comply with GMP standards.
• Participate in production processes and cleanliness checks.
• Perform routine quality checks and inspections.
• Support documentation for nonconformities and CAPA follow-up.
• Review batch records for compliance with GDP standards.

Skills

Knowledge of cGMP regulations

Basic proficiency in statistics

Education

Bachelor’s degree in Pharmaceutical Sciences or Science

Job description

Job Title: Quality Assurance Specialist

Location: Saudi Arabia

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight forHealth 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 forour team members.

Job Summary

We are seeking a passionate and talented Quality Assurance Specialist to join our dynamic team in Saudi Arabia.

Theideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Key Responsibilities

• Monitor environmental conditions and equipment calibration to ensure compliance with GMP standards in all classified production areas.
• Participate in production processes, including raw material dispensing, cleanliness checks, and manufacturing of solid and cephalosporin dosage forms.
• Perform routine quality checks, including in-process inspections, packaging verification, sampling, and warehouse inspections.
• Support deviation handling and documentation, including tracking nonconformities, change controls, and CAPA follow-up.
• Ensure proper documentation and compliance with GDP standards by reviewing batch records, logbooks, and quality reports.

Requirements

• Bachelor’s degree in Pharmaceutical Sciences or Science with 0–3 years of relevant experience.
• Strong knowledge of cGMP regulations, including documentation, inspections, sampling, and contamination prevention.
• Familiarity with quality systems such as CAPA, change control, and ISO 9001 standards.
• Understanding of validation processes, safety programs, and quality compliance protocols.
• Basic proficiency in statistics for quality data interpretation and reporting.
• Saudi manufacturing experience is a MUST.