Quality Assurance Specialist

Eva Pharma; Riyadh; On-site; SAR 150,000 - 200,000; Full time

Job summary

A pharmaceutical company in Saudi Arabia seeks a Quality Assurance Specialist to ensure compliance with GMP standards and support production quality checks. The ideal candidate holds a Bachelor's degree in Pharmaceutical Sciences, has 0–3 years of experience, and must have Saudi manufacturing experience. This role offers the opportunity to contribute to enhancing human health and well-being in a supportive environment.

Qualifications

• 0–3 years of relevant experience in quality assurance.
• Saudi manufacturing experience is a MUST.

Responsibilities

• Monitor environmental conditions and equipment calibration for GMP compliance.
• Participate in production processes including raw material dispensing.
• Perform routine quality checks including in-process inspections.
• Support deviation handling and documentation for tracking nonconformities.
• Ensure documentation compliance with GDP standards.

Skills

cGMP regulations

CAPA

Change control

ISO 9001 standards

Basic proficiency in statistics

Education

Bachelor’s degree in Pharmaceutical Sciences or Science

Job description

Overview

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.

Qualifications

• 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.