227 Assurance Specialist jobs in Saudi Arabia

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.

• 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.

• 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.

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.

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.

• 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.

• 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.

Summary:

QA Specialist is responsible for implementing and executing quality assurance standards and procedures to ensure products/services consistently meet high standards of quality, reliability, and customer satisfaction.

Duties and Responsibilities:

• Collaborate with stakeholders to gather and analyze user requirements.
• Work collaboratively with team members and stakeholders to deliver high-quality software.
• Perform various types of testing, including unit testing, integration testing, system testing, and regression testing.
• Identify areas for improvement in processes, workflows, and systems to enhance quality, efficiency, and minimize errors or defects.
• Identify, document and track software defects using a bug tracking system.
• Analyze test results and provide clear and concise reports on findings.
• Collaborate with developers to understand and resolve identified defects.
• Contribute to the development and maintenance of automated test scripts (if applicable).
• Ensure the changes or deployed effectively and follow MEDGULF IT QA Policy and Procedures
• Participate in test planning and review meetings.
• Ensure the overall quality and stability of applications.
• Any other relevant tasks assigned by the IT management.

Minimum Requirements:

• 2 to 3 years of experience in Quality Assurance Standards
• Experience in planning, conducting, and analyzing usability testing
• Experience with bug tracking systems
• Familiar with software testing methodologies and best practices.
• Strong knowledge about ITIL and related processes.
• Experience with Agile and Scrum methodologies.

Qualification:

• Bachelor's degree in Computer Science, Information Technology, or a related field.
• Certifications in relevant field.

Job Title: Quality Assurance Specialist

Job Responsibilities:

• Implement and follow up on quality policies and procedures within the organization.
• Conduct regular audits of operations and products in accordance with approved standards.
• Continuously improve processes and ensure high-quality outputs.
• Prepare detailed inspection reports and document findings.
• Collaborate with teams to identify issues and recommend appropriate solutions.
• Support internal and external audit processes and ensure readiness.
• Train employees on quality systems and procedures.
• Analyze quality-related data and generate performance indicators.
• Ensure compliance with international standards such as ISO 9001 and others.

Required Qualifications:

• Bachelor's degree in Quality Management, Engineering, Science, or a related field.
• 1 to 3 years of practical experience in quality assurance or a similar field.

Preferred Certifications:

• ISO 9001 Lead Auditor or Internal Auditor
• Six Sigma (any belt level)
• Certified Quality Auditor (CQA)

Required Skills:

• Strong knowledge of quality systems and international standards.
• Excellent analytical skills and attention to detail.
• Proficiency in preparing technical reports and documentation.
• Effective communication and teamwork skills.
• Proficient in Microsoft Office applications.
• English proficiency (reading and writing) is preferred.

Company Description

القلزم يقدم تجارب طعام بحرية فاخرة في جدة والرياض. تشمل خدماتنا تناول الطعام في المطعم، غرف خاصة لكبار الشخصيات، التموين للحفلات الخارجية، وأماكن ترفيهية للعائلات، وكلها مصممة لتقديم لحظات لا تُنسى بجودة وضيافة استثنائية

.

Alqalzam offers premium seafood dining experiences with locations in Jeddah and Riyadh. Our services include in-restaurant dining, private VIP rooms, outdoor catering, and family entertainment options. We are committed to delivering memorable moments with exceptional quality and hospitality

.

Role Description

This is a full-time on-site role located in Jeddah and Riyadh for a Quality Assurance Specialist. The Quality Assurance Specialist will be responsible for ensuring that products and services meet the established standards set by the company. Daily tasks include quality control, quality assurance, quality management, conducting quality audits, and ensuring good manufacturing practice (GMP) compliance. The specialist will also collaborate with various departments to implement and monitor quality control measures

.

Qualifications

• Experience in Quality Control and Quality Assuranc
• eSkills in Quality Management and Good Manufacturing Practice (GMP
• )Proficiency in Quality Auditin
• gStrong analytical and problem-solving skill
• sExcellent communication and teamwork abilitie
• sAttention to detail and a commitment to qualit
• yBachelor's degree in Quality

Company Description

Amana Light, part of RWAZEN Group, is a Saudi Arabian company based in Riyadh, specializing in comprehensive indoor and outdoor lighting systems. We provide clients with the most suitable products for their needs along with full service that resonates with their expectations. Our expertise in lighting solutions helps us deliver top-quality, tailored products and services.

Role Description

This is a full-time, on-site role for a Quality Assurance Specialist based in Riyadh, Saudi Arabia. The Quality Assurance Specialist will be responsible for monitoring and ensuring the quality of indoor and outdoor lighting systems. Daily tasks include performing quality control checks, managing quality assurance processes, adhering to good manufacturing practices, and conducting quality audits. The specialist will also work closely with other departments to maintain consistent quality standards and implement continuous improvement initiatives.

Qualifications

• Quality Control and Quality Assurance skills
• Experience in Quality Management and adhering to Good Manufacturing Practice (GMP)
• Quality Auditing skills
• Strong attention to detail and problem-solving abilities
• Excellent communication and teamwork skills
• Ability to work on-site in Riyadh, Saudi Arabia
• Bachelor's degree in Quality Management, Engineering, or a related field
• Experience in the lighting poles or steel industries.

Company Description

KBE INTERNATIONAL is a leading manufacturer of air movement products for the HVAC market with a focus on quality and safety. The company's products have been tested and certified at renowned laboratories and test facilities, ensuring high performance in various building types and operating conditions. KBE maintains strict quality control standards throughout the manufacturing process and complies with industry regulations and standards set by organizations like UL, ETL-ITS, and AMCA. Based in Riyadh, KBE prides itself on delivering top-notch air distribution solutions for residential, commercial, industrial, and institutional buildings.

Role Description

This is a full-time on-site role for a Quality Assurance Specialist at KBE INTERNATIONAL in Riyadh. The Quality Assurance Specialist will be responsible for overseeing and implementing quality control processes, conducting quality audits, and ensuring compliance with Good Manufacturing Practices (GMP). The role will involve maintaining and improving quality management systems to uphold the company's high standards in air movement product manufacturing.

Qualifications

• Quality Control and Quality Assurance skills
• Experience in Quality Management and Good Manufacturing Practices (GMP)
• Knowledge of Quality Auditing processes
• Strong attention to detail and analytical skills
• Excellent communication and problem-solving abilities
• Certifications in quality management systems (e.g., ISO 9001) is a plus
• Experience in the HVAC industry or manufacturing sector is desirable
• Bachelor's degree in Engineering or related field
• Saudi applicants will be prioritized

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.

We are seeking a detail-oriented and dedicated
Quality Control Specialist
to join our team in the medical devices manufacturing industry. The ideal candidate will have a strong background in chemistry or microbiology, with hands-on experience in quality control testing and compliance with regulatory standards.

Key Responsibilities:

• Perform routine quality control testing of raw materials, in-process samples, and finished medical devices.
• Ensure compliance with ISO standards, GMP, and regulatory requirements.
• Develop, validate, and document laboratory procedures and test methods.
• Conduct microbiological and chemical testing as required.
• Maintain accurate and detailed QC records and reports.
• Support investigations, root cause analysis, and implementation of corrective and preventive actions (CAPA).
• Collaborate with production, QA, and R&D teams to ensure product quality and safety.

Qualifications & Requirements:

• Bachelor's degree in
  Chemistry
  or
  Microbiology
  (or related field).
• Previous experience in
  medical devices
  or
  pharmaceutical/biotech industry
  is preferred.
• Strong knowledge of
  ISO 13485
  ,
  GMP
  , and other regulatory standards.
• Proficiency in laboratory techniques, equipment handling, and data analysis.
• Excellent attention to detail, problem-solving, and communication skills.