261 Head Of Quality jobs in Saudi Arabia

Leverage your abilities and join a leading company specializing in medical device manufacturing in Saudi Arabia.

The Head of Quality Assurance will lead and oversee all quality operations to ensure products meet the highest standards of safety, performance, and compliance with SFDA and ISO 13485 requirements.

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with SFDA and international standards.
• Lead internal and external audits, manage CAPA activities, and ensure continual improvement.
• Monitor and evaluate quality KPIs and performance metrics across all production lines.
• Oversee process validation, supplier qualification, and document control.
• Collaborate with production and R&D to maintain consistent product quality.
• Promote a strong culture of quality awareness and regulatory compliance across departments.
• Ensure staff training, documentation accuracy, and audit readiness at all times.

• Bachelor's degree in Pharmacy, Biomedical Engineering, or Life Sciences (Master's preferred).
• Minimum 10+ years of experience in Quality Assurance within the medical device industry.
• Deep understanding of SFDA requirements, ISO 13485, and GMP standards.
• Strong leadership and analytical skills with proven experience in audit management.
• Excellent command of English; Arabic proficiency is an advantage.

Overview

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 Control Section Head” to join our dynamic team in Sudair City - 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.

• Lead the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation
• Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.
• Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.
• Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.
• Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

• Bachelor’s degree in pharmacy, Chemistry, or Life Sciences.
• 8–10 years in pharmaceutical manufacturing
• Saudi Experience is a Must
• Experience in handling injectables, oral solids, and regulatory audits.
• Strong knowledge of analytical techniques (HPLC, GC, UV, IR).
• Proficient in GMP documentation and data integrity principles.

Job Summary:

We are seeking a passionate and talented "Quality Control Section Head" to join our dynamic team in
Sudair City - 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:
·    Lead the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation

·    Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.

·    Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.

·    Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.

·    Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

Requirements

• Bachelor's degree in pharmacy, Chemistry, or Life Sciences
• 8-10 years in pharmaceutical manufacturing
• Saudi Experience is a Must
• Experience in handling injectables, oral solids, and regulatory audits
• Strong knowledge of analytical techniques (HPLC, GC, UV, IR)
• Proficient in GMP documentation and data integrity principles

Job Summary:

We are seeking a passionate and talented "Quality Control Section Head" to join our dynamic team in Sudair City - 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:·    Lead the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation

·    Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.

·    Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.

·    Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.

·    Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

• Bachelor's degree in pharmacy, Chemistry, or Life Sciences.
• 8–10 years in pharmaceutical manufacturing
• Saudi Experience is a Must
• Experience in handling injectables, oral solids, and regulatory audits.
• Strong knowledge of analytical techniques (HPLC, GC, UV, IR).
• Proficient in GMP documentation and data integrity principles.

Job Summary:

We are seeking a passionate and talented "Quality Control Section Head" to join our dynamic team in Sudair City - 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:

• Lead the setting up of QC laboratories and Plan, coordinate, and execute qualification and calibration of QC instruments, as well as Develop laboratory readiness plan to support site commissioning and validation

• Ensure timely and accurate execution of stability studies and method validations, as well as Review and approve analytical data and reports.

• Ensure adherence to cGMP, SFDA, ICH, FDA, EMA, and other applicable regulatory guidelines.
• Maintain and approve SOPs, STPs, specifications, and other QC documentation and Lead investigations for OOS, deviations, and complaints, ensuring CAPA implementation.
• Prepare for and participate in internal and external audits and ensure timely closure of audit observations and CAPAs.

Requirements

• Bachelor's degree in pharmacy, Chemistry, or Life Sciences.
• 8–10 years in pharmaceutical manufacturing
• Saudi Experience is a Must
• Experience in handling injectables, oral solids, and regulatory audits.
• Strong knowledge of analytical techniques (HPLC, GC, UV, IR).
• Proficient in GMP documentation and data integrity principles.

1. Job Purpose

To ensure the highest standards of service excellence and efficiency across all facets of DACO activities. oversee and guide the developing, implementing and maintaining management system and processes that align with international and aviation regulations and DACO goals. To foster a culture of collaboration with various departments to identify areas of improvement, directing quality inspection and audits, and drive continuous improvement initiatives. This role aims to ensure adherence and compliance to regulatory standards, fostering a culture of excellence, and enhancing overall service quality and operational efficiency.

1. Position Accountability Description

Strategic Leadership

1. Formulate and implement a comprehensive quality management strategy that aligns with DACO’s organizational goals, ensuring adherence to quality standards and regulatory requirements.
2. Oversee the implementation of a quality management system, adopting frameworks such as ISO 9001, to enhance DACO’s performance and maintain high standards of quality.
3. Define key performance indicators (KPIs) to systematically track quality objectives, enabling data-driven decision-making and continuous improvement.

Operational Excellence

1. Direct the development, implementation, and regular updating of management system protocols and documentation to ensure compliance with organizational standards and regulatory requirements.
2. Oversee regular inspections, audits, and performance evaluations of airport facilities and services to ensure regulatory compliance, SLAs, and quality standards.
3. Collaborate with process owners and direct the identification, assessment, and prioritization of opportunities for process improvement using methodologies such as Six Sigma, Lean Management, and Kaizen.
4. Direct the evaluation and analysis of supplier, service, and quality management reports to ensure adherence to standards, while addressing performance issues with actionable insights.
5. Direct the monitoring of quality metrics and lead management reviews to enhance organizational performance and strategic alignment.
6. Direct the risk management process by ensuring implementation and documentation and guide in identifying assessing and mitigating efficient risk management.
7. Direct the establishment, control, and maintenance of all documented information to ensure effectiveness, clarity and traceability.
8. Direct the process of change management to facilitate seamless transitions and minimize negative impact and resistance.
9. Review and update the mitigation plan for external and internal issues related to DACO to maintain operational integrity and to gain interested parties’ confidence.
10. Regularly assess in updating and reviewing the management systems manual to align DACO’s internal requirements and industry best practices.
11. Implement the Total Quality Management (TQM) principles to foster a culture of continuous improvement and customer centricity.
12. Direct the interpretation of policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
13. Direct the process analyses oversights on a continuing basis to implement a culture of excellence by working directly with operating entities.
14. Direct the establishment, implementation, and management of quality management systems, incorporating internationally recognized frameworks like ISO 9001.

Stakeholder Management

1. Cultivate strong relationships with key stakeholders, including vendors, internal departments, and external partners, to be up to date with their needs and expectations and ensure effective management of quality initiatives and adherence to quality standards.
2. Work with vendors to negotiate quality-related contracts and secure optimal solutions for DACO’s quality management needs, fostering continuous improvement and alignment with business objectives.
3. Ensure that quality management activities align with DACO’s strategic goals by collaborating closely with internal and external stakeholders to gather resources and information needed for successful implementation.

Team Leadership and Development

1. Lead, mentor, and develop a high-performing quality management team, promoting a culture of excellence, accountability, and continuous improvement.
2. Establish clear performance expectations for team members, providing regular feedback and support to foster their growth and development.
3. Create and implement training programs to enhance the skills and knowledge of the quality management team, ensuring they are prepared to meet evolving industry challenges and maintain high standards.

Financial Management

1. Oversee the budget for quality management activities, ensuring cost-effectiveness and efficient resource allocation to maximize return on investment.
2. Track the financial performance of quality management initiatives, identifying cost-saving opportunities and implementing measures to achieve financial targets.
3. Manage financial planning within the department, monitoring expenditures to ensure adherence to budgetary guidelines and financial targets.

Innovation and Continuous Improvement

1. Foster innovation in quality management by adopting new technologies and best practices, ensuring DACO remains at the forefront of industry advancements.
2. Regularly assess and enhance quality management processes to improve efficiency, effectiveness, and alignment with DACO’s strategic objectives.
3. Promote a culture of continuous improvement within the team by actively seeking and implementing feedback and ideas for process enhancements.

Join the Team at
ABYAT
- Your Gateway to Retail Excellence

About us

Are you ready to be part of the largest retail store in the Middle East?
ABYAT
, spanning an impressive 22,000 square meters and offering over 22,000 products, is your one-stop destination for all things home improvement and more. From elegant tiles and captivating wallpapers to state-of-the-art lighting solutions and stylish kitchen fixtures, we pride ourselves on offering a diverse array of top-quality products under one roof.

Established locally with a vision for excellence,
ABYAT
has been setting benchmarks since its inception in September 2005. With an unwavering focus on our customers, we've crafted an experience that revolves around their needs, from our meticulously designed store layouts to our unparalleled service offerings.

Expanding beyond our roots in Kuwait,
ABYAT
is now making waves in Saudi Arabia and setting our sights on Qatar and the UAE. As we continue to grow, we're seeking passionate individuals to join our dynamic team and contribute to our journey of success.

Position
: Inbound Quality inspector

Location
: Saudi Arabia – Jeddah

Type
: Full-time

Role Purpose

The QMS Auditor's role is to check if the company's Quality Management System (QMS) is working properly and follows standards like ISO 9001. The auditor does this by performing regular internal audits to make sure the company meets its own policies, SOPs, quality goals & Legal rules. The auditor also helps find gaps, suggests improvements, and supports continuous development. This role is important for reducing risks, improving operations, and helping the company keep its quality certifications by giving clear and efficient feedback to the management.

Duties and Responsibilities

• Conduct periodic audits of warehouses, factories, and field installation teams to verify compliance with quality standards and to ensure alignment with established procedures.
• Supplier On-Site Audits
• Perform on-site inspections of Finishing and Furnishing installations, ensuring compliance with the required technical specifications.
• Prepare detailed audit reports, identify non-conformities, risks, and opportunities for improvement; prepare clear and concise audit reports.
• Follow up on corrective and preventive actions (CAPAs) and verify their implementation and effectiveness.
• Collaborate with process owners to support continuous improvement and best practices.
• Assist in preparing for external audits and certifications.
• Maintain accurate and updated audit records and documentation.

Qualifications/Requirements:

Required Experience

• A minimum of 3 to 5 years of practical experience in internal auditing, quality management and auditing
  operational processes (Manufacturing – Aftersales – Logistics).
• Solid knowledge of quality management systems (e.g., ISO 9001) and Workplace health and safety standards (OSHA).
• Proven experience in auditing manufacturing operations, Logistics, and field installation teams.
• Familiarity with the materials and techniques used in manufacturing and installing aluminum products for windows, doors, and kitchens.
• Proficiency in using computers and report preparation tools.
• It is required that the candidate has good knowledge of the SAP system.

Knowledge and Skills

• Strong knowledge of ISO 9001:2015 standard and quality management principles.
• Familiarity with risk-based thinking, process auditing, and continual improvement techniques.
• Understanding of relevant industry regulations and standards.
• Analytical thinking and attention to detail.
• Strong communication and reporting skills.
• High level of integrity, objectivity, and impartiality.
• Ability to manage time and priorities effectively.

Comfortable working independently and in teams

Education and Certifications

• High School Diploma in Quality Management, Industrial technology, or Business Administration (with quality focus)
• Internal Auditor Certification (ISO 9001 or other applicable standards like ISO 14001, ISO 45001, etc.).

Leverage your abilities and join a leading company specializing in medical device manufacturing in Saudi Arabia.

The Head of Quality Assurance will lead and oversee all quality operations to ensure products meet the highest standards of safety, performance, and compliance with SFDA and ISO 13485 requirements.

• Develop, implement, and maintain the company’s Quality Management System (QMS) in compliance with SFDA and international standards.

• Lead internal and external audits, manage CAPA activities, and ensure continual improvement.

• Monitor and evaluate quality KPIs and performance metrics across all production lines.

• Oversee process validation, supplier qualification, and document control.

• Collaborate with production and R&D to maintain consistent product quality.

• Promote a strong culture of quality awareness and regulatory compliance across departments.

• Ensure staff training, documentation accuracy, and audit readiness at all times.

• Bachelor’s degree in Pharmacy, Biomedical Engineering, or Life Sciences (Master’s preferred).

• Minimum 10+ years of experience in Quality Assurance within the medical device industry.

• Deep understanding of SFDA requirements, ISO 13485, and GMP standards.

• Strong leadership and analytical skills with proven experience in audit management.

• Excellent command of English; Arabic proficiency is an advantage.

Regional Head of Quality & Food Safety – MENAI

Location:
Jeddah, Saudi Arabia

About the Business

Alexander Steele Recruitment have partnered with a global leader in the Food & Beverage industry, home to some of the most iconic brands worldwide. With a workforce of over 16,000 employees, the business is entering an exciting new phase of growth and innovation across the MENAI region. To support this, they are seeking an accomplished Quality & Food Safety leader to oversee the Regional QFS agenda across Saudi Arabia, Egypt, India and the wider MENAI framework.

The Role

The
Regional Head of Quality & Food Safety
will lead and shape the QFS function across MENAI, ensuring compliance with industry standards, legislation, and food safety requirements. Sitting as part of the Global QFS Council, this role will drive consistency, governance and continuous improvement, while future-proofing the organisation against risks and building world-class standards across suppliers, co-packers, manufacturing and storage sites.

Key Responsibilities

• Lead, manage and develop regional QFS teams across Crisis Management, Retailer Technical Management, and Food Safety.
• Drive compliance, consistency, and standardisation across MENAI sites.
• Set strategic goals, metrics and reviews in alignment with the global QFS strategy.
• Audit and approve 600+ raw material and packaging suppliers, ensuring robust Food Safety and Quality Systems.
• Manage relationships with external Food Safety and Quality service providers.
• Monitor and communicate food industry updates and regulatory changes.
• Benchmark against industry best practice through external bodies, suppliers and customers.
• Act as QFS lead on global business-wide initiatives, supporting simplification and functional alignment.

What We're Looking For

• Proven track record in a cross-regional Quality & Food Safety leadership role.
• Strong knowledge of global industry standards and regulatory requirements.
• Degree in Food Science or a related discipline.
• Experienced in stakeholder engagement and managing complex supplier networks.
• Agile, resilient and collaborative leader able to operate in a dynamic, matrix organisation.

Why Apply?

This is a rare opportunity to take ownership of the Quality & Food Safety agenda for a truly global business in a critical growth region. You'll shape future strategy, represent MENAI on a global stage, and lead a diverse, high-performing team.