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 seeking a Quality Assurance Specialist to join their dynamic team. The ideal candidate will ensure compliance with GMP standards and contribute to enhancing human health and well-being. Responsibilities include monitoring environmental conditions, performing routine quality checks, and supporting deviation handling. Candidates should possess a Bachelor's degree in Pharmaceutical Sciences or Science and have knowledge of cGMP regulations, with Saudi manufacturing experience being mandatory.

Qualifications

• Strong knowledge of cGMP regulations, including documentation and inspections.
• Familiar with quality systems such as CAPA and ISO 9001.
• Saudi manufacturing experience is a MUST.

Responsibilities

• Monitor environmental conditions and equipment calibration.
• Participate in raw material dispensing and cleanliness checks.
• Perform routine quality checks and packaging verification.

Skills

Knowledge of cGMP regulations

Understanding of validation processes

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 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.

Job Summary

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

The ideal 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.