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Job Title: Quality Specialist

Location: Saudi Arabia, Riyadh

Job Type: Full-Time

Job Summary: We are looking for a Quality Specialist to join our team and contribute to enhancing operational efficiency and achieving the highest quality standards.

Key Responsibilities:

• Monitor the implementation of quality procedures and policies.
• Review and update operational procedures to improve efficiency and reduce errors.
• Conduct field visits to ensure compliance with quality standards.
• Identify operational issues and propose and implement appropriate solutions.
• Manage and execute continuous improvement plans and development projects.
• Handle complaints and feedback to ensure customer satisfaction.

Qualifications:

• Diploma or Bachelor’s degree in Business Administration or a related field.
• 23 years of experience in quality or process improvement.
• Knowledge of quality standards and systems (*, ISO 9001) is an advantage.
• Strong analytical and problem-solving skills, with the ability to work in the field.

Working Conditions: Full-time role with possible shift work.

Join EVA Pharma as a Quality Control Specialist!
We are a leading pharmaceutical company dedicated to empowering health and well-being as a fundamental human right. As a recognized best place to work, we foster 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. You will contribute to our mission of enhancing human health and ensuring that we meet the highest standards of excellence in our industry.

Key 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 according to 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.

Requirements:

• Bachelor's degree in Science, Biotechnology, or Pharmacy with 02 years of relevant lab experience.
• Basic knowledge of GMP/GLP, lab safety, wet chemistry techniques, and instruments like HPLC and UV-Vis.
• Strong attention to detail, time management, adaptability, teamwork, and communication skills.
• 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.

Note: Saudi manufacturing experience is a MUST.