556 Quality 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 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.

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.

• 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.

The Quality Specialist is responsible for monitoring and maintaining product and service quality standards to enhance customer satisfaction and ensure compliance with regulatory and company standards. This role involves supporting the commercial teams by identifying improvement areas, implementing quality control measures, and coordinating corrective actions to ensure consistent quality in products, processes, and services.

• Quality Monitoring & Inspection: Perform regular checks on commercial products and services, ensuring they meet company quality standards and specifications. Collaborate with suppliers and vendors to address quality concerns.
• Customer Complaint Handling: Investigate and analyze customer complaints related to product quality or service. Identify root causes and work with relevant teams to implement corrective actions to prevent recurrence.
• Documentation & Compliance: Ensure all documentation related to quality standards, audits, and corrective actions is accurately maintained. Support compliance with applicable regulations, industry standards, and company policies.
• Process Improvement: Support continuous improvement initiatives by analyzing data, identifying areas for enhancement, and suggesting process adjustments to improve efficiency, reduce costs, and increase customer satisfaction.
• Supplier & Vendor Management : Work closely with the purchasing team to assess and monitor supplier quality performance, ensure supplier compliance with company standards, and support supplier audits.
• Training & Support: Provide training to the employees and support teams on quality standards, policies, and procedures. Promote a quality-focused culture across departments to enhance awareness and commitment.

• Customer Complaint Resolution Time: Achieve an average resolution time of 7 working days for customer complaints.
• Product Return Rate: Maintain a product return rate of X% (set by management) or below.
• Compliance Rate: Ensure 100% compliance with regulatory and company quality standards.
• Supplier Quality Compliance: Achieve X% (set by management) of suppliers meeting company quality standards consistently.
• Process Improvement Initiatives : Successfully implement X (set by management) quality improvement initiatives per year.

• Education : Diploma or bachelor’s degree in a related field.
• Experience: Minimum 1-2 years of experience in quality assurance, compliance, or a similar role in a commercial or retail environment.
• Certifications: Certification as a Certified Quality lead audit, Certified Quality Technician, or similar is preferred.

• Technical Knowledge : Familiarity with quality management systems (QMS), ISO standards, and data analysis tools.
• Skills: Strong analytical skills, problem-solving, and attention to detail with the ability to work across various departments.
• Abilities: Capable of managing multiple tasks effectively and working in a fast-paced commercial environment.

• Language Requirements: Fluent in English; proficiency in additional languages is a plus.
• Communication Skills : Excellent verbal and written communication skills, with the ability to work effectively with internal teams and external partners.

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.

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.

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.

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

Oversee Quality Control and Assurance for raw materials, products, and machinery to ensure compliance with SPC's standards, customer requirements, and operational plans. Support management through KPIs, audits, customer satisfaction tracking, and supplier evaluations.

Key Responsibilities:

• Review and align SPC's Quality Management System (QMS) with international standards; implement necessary updates.
• Communicate and train teams on quality inspection and testing changes.
• Approve or escalate rejection notes; coordinate with Engineering and Production to resolve quality issues.
• Ensure non-compliant products are held until properly reviewed and approved.
• Develop and monitor corrective/preventative actions to address quality concerns.
• Handle customer complaints through root-cause analysis and action plans.
• Identify improvement opportunities in processes, costs, and productivity.
• Ensure daily operations comply with SPC policies and procedures.

Requirements:

• Experience:
  4+ years in Quality Control/Assurance; Internal Auditing and Lean Manufacturing preferred.
• Education:
  Bachelor's in Industrial or Mechanical Engineering.
• Certifications:
  ISO 14001 and ISO or equivalent).