Quality Control Specialist

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

Job summary

A leading pharmaceutical company is seeking a Quality Control Specialist in Saudi Arabia. The role involves performing tests on materials, ensuring compliance with industry standards, and contributing to health and well-being. Candidates should have a Bachelor's degree in Science or a related field and ideally have Saudi manufacturing experience. This position offers an opportunity to work in a supportive and innovative environment.

Qualifications

• 0–2 years of relevant lab experience required.
• Basic knowledge of GMP/GLP and lab safety.
• Proficiency in Microsoft Office and LIMS.

Responsibilities

• Perform chemical and physical tests on raw materials and products.
• Ensure adherence to cGMP, GLP, and SOPs.
• Operate, calibrate, and maintain laboratory instruments.

Skills

Attention to detail

Time management

Adaptability

Teamwork

Communication

Problem-solving

Education

Bachelor's degree in Science, Biotechnology, or Pharmacy

Tools

HPLC

GC

UV-Vis

Job description

Overview

Job Title: Quality Control 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 Control 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.

Responsibilities

• Perform chemical and physical tests on raw materials, intermediates, and finished products using techniques like HPLC, GC, UV, and FTIR.
• Ensure adherence to cGMP, GLP, and SOPs; accurately record test results, deviations, and observations.
• Operate, calibrate, and maintain laboratory instruments per schedule and SOPs.
• Handle sample receiving, labeling, and traceability; ensure data integrity and proper documentation practices.
• Assist with method development, audits, training, and inventory/reagent management while contributing to continuous improvement efforts.

Qualifications

• Bachelor's degree in Science, Biotechnology, or Pharmacy with 0–2 years of relevant lab experience.
• Basic knowledge of GMP/GLP, lab safety, wet chemistry techniques, and use of instruments like HPLC and UV-Vis.
• Strong attention to detail, time management, adaptability, teamwork, and communication.
• Proficiency in Microsoft Office and basic LIMS or digital documentation systems.
• Demonstrated reliability, receptiveness to feedback, problem-solving ability, and focus on regulatory compliance and data accuracy.
• Saudi manufacturing experience is a MUST.