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quality assurance

VITROLIFE

<div><p><i>At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.</i></p><p><b><br>
Make Quality Matter &mdash; Where It Impacts Lives.</b></p><p>
We are looking for a <b>Quality Assurance Specialist</b> to strengthen and advance our local quality operations in Riyadh. This role sits at the intersection of <b>regulatory excellence, operational quality, and continuous improvement</b>, ensuring that our laboratory services meet the highest international and local standards.</p><p>
You will play a key role in <b>driving compliance, enabling safe and effective services, and embedding a proactive quality culture</b> &mdash; working closely with both local teams and regional quality leadership.</p><h4 class="jobSectionHeader"><b><br>
Your Impact</b></h4><p>
As a Quality Assurance Specialist, you will:</p><h6 class="jobSectionHeader"><b>
Drive Quality Operations &amp; Compliance</b></h6><ul><li><p>
Oversee day-to-day quality activities and ensure adherence to local and regional requirements</p></li><li><p>
Maintain accurate quality records and actively participate in quality management forums</p></li><li><p>
Ensure compliance with <b>MOH, SFDA, CBAHI</b>, and other applicable regulations</p></li></ul><h6 class="jobSectionHeader"><b>
Strengthen the Quality Management System (QMS)</b></h6><ul><li><p>
Manage document control processes to ensure procedures are current, compliant, and accessible</p></li><li><p>
Support implementation and updates of local and global procedures</p></li><li><p>
Contribute to continuous improvement of QMS processes</p></li></ul><h6 class="jobSectionHeader"><b>
Lead Audits, Risk &amp; Continuous Improvement</b></h6><ul><li><p>
Plan and conduct internal audits; manage findings and CAPA implementation</p></li><li><p>
Support external audits and regulatory inspections</p></li><li><p>
Lead local risk assessments and foster a proactive risk management culture</p></li></ul><h6 class="jobSectionHeader"><b>
Manage Deviations, CAPA &amp; Performance</b></h6><ul><li><p>
Investigate deviations and ensure effective CAPA closure</p></li><li><p>
Monitor KPIs, incidents, and nonconformities</p></li><li><p>
Identify trends and escalate critical insights to Regional Quality Management</p></li></ul><h6 class="jobSectionHeader"><b>
Enable Regulatory &amp; Operational Excellence</b></h6><ul><li><p>
Monitor regulatory changes and ensure timely implementation</p></li><li><p>
Support licensing, certifications, and renewals</p></li><li><p>
Ensure quality alignment in new or modified services</p></li></ul><h6 class="jobSectionHeader"><b>
Collaborate &amp; Build Capability</b></h6><ul><li><p>
Train and support staff on quality and regulatory requirements</p></li><li><p>
Evaluate the external critical suppliers/service provider and referral laboratories to ensure compliance</p></li><li><p>
Contribute to regional and global quality initiatives and harmonization efforts</p></li></ul><h4 class="jobSectionHeader"><b>
Who You Are</b></h4><p>
You are a <b>structured, analytical, and proactive quality professional</b> who thrives in regulated environments and enjoys collaborating across teams.</p><h4 class="jobSectionHeader"><b>
Qualifications</b></h4><ul><li><p>
Bachelor&rsquo;s degree in Laboratory Sciences, Biomedical Sciences, or related field</p></li><li><p>
SCFHS license (preferred)</p></li><li><p>
Certification in Quality Assurance or Regulatory Affairs is a plus</p></li></ul><h4 class="jobSectionHeader"><b>
Experience</b></h4><ul><li><p>
3&ndash;4 years in a similar QA/regulatory role</p></li><li><p>
Experience within laboratory or medical environment</p></li><li><p>
Strong knowledge of:</p><ul><li><p><b>
MOH and SFDA regulations</b> <i>(required)</i></p></li><li><p><b>
CBAHI standards</b> <i>(required)</i></p></li><li><p><b>
ISO 15189 and CAP accreditation</b> <i>(preferred)</i></p></li></ul></li></ul><h4 class="jobSectionHeader"><b>
Skills</b></h4><ul><li><p>
Strong understanding of QMS, audits, and documentation</p></li><li><p>
Experience with QMS/LIS systems</p></li><li><p>
Excellent problem-solving and organizational skills</p></li><li><p>
Strong communication and collaboration abilities</p></li><li><p>
Fluent in <b>Arabic and English</b> (written and spoken)</p></li></ul><p></p><h4 class="jobSectionHeader"><b>
What You Bring Beyond the Basics</b></h4><ul><li><p>
A <b>proactive mindset</b> &mdash; you don&rsquo;t wait for issues, you prevent them</p></li><li><p>
The ability to <b>translate regulations into practical, working processes</b></p></li><li><p>
Confidence to <b>challenge, improve, and influence</b></p></li><li><p>
A strong sense of <b>ownership and accountability</b></p></li></ul><h4 class="jobSectionHeader"><b>
Why Join Us</b></h4><ul><li><p>
Be part of an organization where <b>quality is central to patient impact</b></p></li><li><p>
Work in a <b>collaborative regional and global environment</b></p></li><li><p>
Contribute to <b>high-standard laboratory services and continuous improvement</b></p></li><li><p>
Grow within a culture that values <b>expertise, structure, and innovation</b></p></li></ul><p></p><h6 class="jobSectionHeader"><b>
Additional Information</b></h6><ul><li><p>
Preference will be given to <b>Saudi Nationals</b></p></li></ul><p><i>
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.</i></p><p><i>
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.</i></p></div><p></p>

Quality Assurance Specialist

SARJ

<div><h3 class="jobSectionHeader"><b>Company Overview</b></h3><p>
Built with in KSA with Silicon Valley experience, we're building a suite of products across Voice AI &amp; AI agents. We're a small team that's growing rapidly and are on the cusp of hyper growth in an extremely exciting market. If you're looking to join a fast-paced, growing start-up, then this is the place for you!</p><h3 class="jobSectionHeader"><b><br>
Role Overview</b></h3><p>
As a <b>Quality Assurance Intern</b>, you'll work closely with our engineering and product teams to ensure the quality, reliability, and performance of our products. You'll contribute to testing processes, identifying bugs, and improving product quality across various stages of development. This is an opportunity to gain hands-on experience in QA practices within a high-growth AI start-up environment.</p><p></p><h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><ul><li><p>
Assist in designing, developing, and executing test plans and test cases</p></li><li><p>
Perform manual and automated testing to ensure product quality</p></li><li><p>
Identify, document, and track bugs and issues using appropriate tools</p></li><li><p>
Collaborate with engineering and product teams to resolve defects</p></li><li><p>
Participate in regression, functional, and performance testing</p></li><li><p>
Help improve QA processes, testing frameworks, and best practices</p></li><li><p>
Support release cycles by validating features before deployment</p></li><li><p>
Contribute to documentation of test cases, results, and QA procedures</p></li></ul><p></p><h3 class="jobSectionHeader"><b>
Requirements</b></h3><ul><li><p>
Final semester or recent university graduate in Computer Science, Engineering, or related field</p></li><li><p>
Interest in software quality assurance, testing, and AI technologies</p></li><li><p>
Basic understanding of software testing concepts and methodologies</p></li><li><p>
Strong attention to detail and problem-solving skills</p></li><li><p>
Excellent communication and analytical abilities</p></li><li><p>
Eagerness to learn and adapt in a fast-paced environment</p></li><li><p>
Ability to speak and write fluently in both Arabic &amp; English</p></li><li><p>
Familiarity with testing tools or programming languages is a plus</p></li><li><p>
Based in KSA, preferably Riyadh</p></li></ul><p></p><h3 class="jobSectionHeader"><b>
Why Join Us?</b></h3><ul><li><p>
Opportunity to be part of a high-growth, innovative tech start-up</p></li><li><p>
Collaborative, mission-driven culture</p></li><li><p>
Hands-on experience working on impactful AI products</p></li><li><p>
Exposure to real-world QA processes and modern testing tools</p></li></ul></div>

Quality Assurance Intern

Jeddah Cables Company

<p><b>Quality Assurance (QA) Engineer in a Jeddah cables manufacturing company</b> is responsible for making sure that all cables meet required standards, safety regulations, and customer specifications before they reach the market.</p><p>Key Responsibilities</p><ul><li><b>Quality Control Testing</b></li><li>Perform tests on raw materials (copper, aluminum, insulation)</li><li>Check finished cables for strength, conductivity, insulation resistance, etc.</li><li><b>Standards Compliance</b></li><li>Ensure products meet standards like <b>IEC, ASTM, ISO</b></li><li>Follow internal quality procedures and documentation</li><li><b>Process Monitoring</b></li><li>Monitor production lines (extrusion, stranding, armoring)</li><li>Identify defects and suggest corrective actions</li><li><b>Inspection &amp; Audits</b></li><li>Conduct in-process and final inspections</li><li>Participate in internal and external audits</li><li><b>Documentation</b></li><li>Maintain test reports, inspection records, and quality logs</li><li>Prepare certificates of conformity (CoC)</li><li><b>Problem Solving</b></li><li>Investigate defects (e.g., insulation failure, diameter variation)</li><li>Work with production teams to improve processes</li></ul><p>Work Location: In person</p>

Quality Assurance Engineer

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<div><b>Location: Saudi Arabia, Riyadh</b></div>
<div><b>
Job Type: [Full-time]</b></div>
<div><b>
Hashtag: #LI-NA1</b></div><br>
<div></div>
<div><b>
About Us:</b></div>
<div>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</div><br>
<div></div>
<div>
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</div><br>
<div></div>
<div><b>
Description:</b></div><br>
<div></div>
<div>
We are looking for a talented <b>Quality Assurance Officer </b>to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</div><br>
<div></div>
<div>
If you want to be part of a team that cares about impact, this is the place for you.</div><br>
<div></div>
<p><b>
Key Responsibilities:</b></p>
<div>
<ul><li><b> </b>Directly responsible for quality assurance of the pharmaceutical drug products by enforcing SFDA requirements, Good Manufacturing Practices, and other quality related tools in order to meet the quality regulations.</li></ul>
</div><div><ul><li>Review drug product Batch Records and other manufacturing related documents to verify compliance and record keeping for all mandated manufacturing process, quality checks, testing, sampling, and sanitization activities.</li></ul>
<ul><li>Quality Audits related to API, Packaging Components, Labels, and finished products to ensure compliance with established specifications and regulatory standards.</li></ul>
<ul><li>Follow up with implemented programs (GMPs, Good Hygiene Practices, HACCP, Allergen Control, Cleaning and Sanitization, Pest Control, Equipment Calibration etc.) to ensure compliance by all employees and other personnel involved in the production process in the manufacturing facility.
</li></ul><ul><li>Co-ordinate for the testing results availability involving finished products, raw materials and packaging components and the appropriate release and hold programs associated with these materials.</li></ul>
<ul><li>Oversee the &ldquo;On Hold&rdquo; product program, including the status, release and destruction of Drug Products including its tailings.</li></ul>
<ul><li>Assist in investigating and correcting quality-related issues (including customer complaints) through proper collaboration with other departments.</li></ul>
<ul><li>Ensure good performance by quality assurance by mentoring, training, setting expectations, providing accountability evaluations.
</li></ul><ul><li>Perform other Quality Assurance duties as directed by the Quality Assurance Supervisor.</li></ul>
<ul><li>Responsible to maintain competence in all responsibility of a Quality Assurance Officer.</li></ul><br>
</div>
<div></div><div><b>Qualifications:</b></div>
<div><b>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</b></div><br>
<div></div>
<div><b>
Education: </b>Bachelor&rsquo;s degree in Chemist, Chemical Engineering and Pharmacist.</div>
<div><b>
Experience</b>: 0-3 years.</div><br>
<div></div>
<div><b>
Learn more about Hikma in KSA </b><b>hikma-ksa-factsheet-aug-2025-en.pdf</b></div>
</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div><p></p>

Quality Assurance Officer (Trainee)

Almarai - المراعي

<div>
 <p>
  <strong>
   QA Technician | Saudi Arabia, Jeddah
  </strong>
 </p>
 <p>
  <strong>
  </strong>
 </p>
 <p>
  <strong>
   The Company:
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Founded in 1977, Almarai Company is the world&rsquo;s largest vertically integrated dairy company and the largest food and beverage manufacturing and distribution company in MENA. Headquartered in Riyadh, Almarai Company is ranked as the number one FMCG Brand in the MENA region and the market leader in all its categories across GCC, Egypt, and Jordan.
 </p>
 <p>
  Over five decades of sustainable growth, Almarai has consistently provided nutritious and healthy products to consumers of all ages, driven by its core principle: &ldquo;Quality you can trust.&rdquo;
 </p>
 <p>
  Almarai has expanded its product range to include, in addition to dairy products, juices and beverages, baked goods, poultry, infant formula, dates, fish and seafood, and bottled water, under more than 20 brands such as Almarai, L&rsquo;usine, 7DAYS, ALYOUM, Nuralac, Farm&rsquo;s Select, Ice Leaf, Almira, Seama, Oska, IVAL, Almara Pro, Premier Chef, Bakemart, and others.
 </p>
 <p>
  Almarai currently employs over 43,000 Quality Makers, across the GCC, Egypt &amp; Jordan.
 </p>
 <p>
  In 2025, Almarai reported net income of SAR 2.4 billion on sales of SAR 22 billion.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About the role:
  </strong>
 </p>
 <p>
  To handle RDNCNs and investigate minor QA related issues in the area of warehouse, transport, workshop and yard operation.
 </p>
 <p>
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 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Manage and follow up on Reefer Delivery Non‑Compliance Notifications (RDNCN) raised by the Sales Division.
  </li>
  <li>
   Conduct regular Good Hygiene Practice (GHP) audits across the Transportation &amp; Logistics (T&amp;L) operations.
  </li>
  <li>
   Perform Pre‑Requisite Program (PRP) verifications in line with quality and food safety standards.
  </li>
  <li>
   Support the maintenance and updating of QA databases, including GHP audit records, training logs, and QA monitoring sheets through data collection and verification.
  </li>
  <li>
   Assist in the preparation of weekly and monthly KPI reports.
  </li>
  <li>
   Monitor Non‑Conformance Notices (NCNs) and ensure timely follow‑up and closure of corrective actions with relevant stakeholders.
  </li>
 </ul>
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 </p>
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  <strong>
   Requirements:
  </strong>
 </p>
 <ul>
  <li>
   Diploma holder in any science discipline.
  </li>
  <li>
   1 Year of working experience in quality function in FMCG environment
  </li>
  <li>
   English Fluency
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
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 </p>
 <p>
  Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.
 </p>
 <p>
  <br/>
 </p>
 <p>
  This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package.
 </p>
</div>


Quality Assurance Technician

2P Perfect Presentation

<div>
 <p>
  We are looking for an experienced
  <strong>
   Software Quality Engineer
  </strong>
  to join our team and ensure the quality, performance, and reliability of large-scale IT systems.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Prepare and execute various types of software testing to ensure system quality, performance, and functionality.
  </li>
  <li>
   Identify, analyze, and report system defects and issues.
  </li>
  <li>
   Test technical changes in pre-production environments.
  </li>
  <li>
   Prepare and document technical change testing reports.
  </li>
  <li>
   Collaborate closely with development and technical teams to ensure quality standards are met.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements:
  </strong>
 </p>
 <ul>
  <li>
   Minimum
   <strong>
    5 years of experience
   </strong>
   in software quality testing.
  </li>
  <li>
   Hands-on experience in testing large-scale IT systems.
  </li>
  <li>
   Strong knowledge of software testing methodologies and QA best practices.
  </li>
  <li>
   High attention to detail with strong analytical skills.
  </li>
  <li>
   Ability to work effectively within a team environment.
  </li>
 </ul>
</div>


Adree

<div>Roles &amp; Responsibilities<ul><li>
Implement quality assurance strategies and methodologies for products and systems, and ensure the application of quality standards.</li><li>
Align solution and product development processes with policies, procedures, and standards throughout the lifecycle of systems and applications.</li><li>
Ensure compliance with product and project development procedures across all methodologies, including Agile and DevOps, from analysis through release.</li><li>
Review different business functions to support and enhance quality assurance strategies.</li><li>
Coordinate with business analysts, developers, system testers, and stakeholders to ensure adherence to quality standards.</li><li>
Conduct audits and review activities to identify potential issues and ensure end-to-end quality.</li><li>
Prepare quality output reports for stakeholders and ensure all processes and products comply with defined standards.</li><li>
Perform any additional tasks as assigned.</li></ul><br>
<b>
Requirements</b><p><br>
Bachelor&rsquo;s degree in Computer Science, Management Information Systems, or equivalent.</p><p>
Master&rsquo;s degree in Computer Science, Business Administration, or equivalent is preferred.</p><p>
Preferred professional certifications: Six Sigma, CSM (Scrum/CSM), ITIL, ISO 9001, and ISO 20000-1.</p></div>

Software Quality Assurance (SQA)

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Software Quality Assurance (SQA)