planning engineer Jobs in Jeddah Saudi Arabia

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qa/qc architect Jobs in Jeddah Saudi Arabia

qa/qc architect

qa/qc civil engineer (aramco approved) Jobs in Jeddah Saudi Arabia

qa/qc civil engineer (aramco approved)

quality assurance executive Jobs in Jeddah Saudi Arabia

quality assurance executive

qa qc architect

Surbana Jurong Private Limited

<div><div>About Surbana Jurong</div><div>
Surbana Jurong (SJ) is a leading global urban, infrastructure, and managed services consulting firm, driven by a vision to build cities and shape lives. Headquartered in Singapore, SJ is a diverse collective of experts delivering sustainable and high-impact solutions across the built environment.</div><div></div><div>
The Role</div><div>
As part of our Architecture team, the QA/QC Architect will play a key role in ensuring design and documentation quality across multiple building projects. This role involves reviewing architectural deliverables to ensure alignment with design intent, technical standards, and client requirements, while promoting a culture of continuous improvement and design excellence. The QA/QC Architect will work closely with design teams, project managers, and multidisciplinary teams to uphold Surbana Jurong&rsquo;s commitment to quality and compliance.</div><div></div><div>
Key Responsibilities</div><ul><li><div>
Review and audit architectural drawings, specifications, and deliverables to ensure compliance with project requirements, codes, and company standards.</div></li><li><div>
Establish and maintain QA/QC procedures, checklists, and review processes to enhance design and documentation quality.</div></li><li><div>
Coordinate with project architects, engineers, and consultants to resolve design discrepancies and ensure consistency across disciplines.</div></li><li><div>
Conduct periodic quality reviews at various project stages (concept, schematic, detailed design, and construction documentation).</div></li><li><div>
Support teams in implementing corrective actions and lessons learned from previous quality audits.</div></li><li><div>
Contribute to continuous improvement initiatives within the Architecture discipline to streamline workflows and enhance technical accuracy.</div></li><li><div>
Ensure all deliverables adhere to client specifications, regulatory requirements, and Surbana Jurong&rsquo;s internal QA/QC framework.</div></li></ul><div></div><div>
Key Qualifications and Experience</div><ul><li><div>
Bachelor&rsquo;s degree in Architecture from a recognized university.</div></li><li><div>
8&ndash;12 years of experience in architectural design, quality control, or design management within a consultancy or multidisciplinary environment.</div></li><li><div>
Strong understanding of design processes, documentation standards, and quality management systems.</div></li><li><div>
Proven experience reviewing and coordinating architectural and multidisciplinary design packages for large-scale projects.</div></li><li><div>
Familiarity with regional and international building codes, standards, and best practices.</div></li><li><div>
Experience in PMC or design review roles within major building or infrastructure projects is an advantage.</div></li></ul><div></div><div>
Key Knowledge and Skills</div><ul><li><div>
Proficiency in design and review tools such as AutoCAD, Revit, and BIM-based coordination platforms.</div></li><li><div>
Excellent attention to detail and ability to identify technical inconsistencies and design issues.</div></li><li><div>
Strong understanding of QA/QC principles, documentation workflows, and version control systems.</div></li><li><div>
Effective communication, coordination, and stakeholder management skills.</div></li><li><div>
Ability to work collaboratively across multidisciplinary teams and mentor junior architects on quality processes.</div></li></ul><div></div><div>
How to Apply</div><div>
Please submit your application through our official careers portal. Click on the &ldquo;Apply Now&rdquo; button below and follow the instructions.</div><div>
Note: Recruitment for this role is managed internally. Unsolicited CVs from recruitment agencies will not be considered.</div><div></div><div>
At Surbana Jurong, we put talent, hard work, teamwork and a fun workplace together to approach problems and solve them creatively and collaboratively. Join us in making a positive impact on the world!</div></div>

QA/QC Architect

Petroraq Engineering

<p>Job Purpose</p><p>To ensure all civil works (earthworks, concrete, structural, finishing, roadworks, etc.) in Aramco projects are executed in full compliance with Aramco standards, project specifications, applicable codes, and quality procedures through systematic inspection, documentation, and quality assurance activities.</p><p>Key Responsibilities</p><ul><li>Review and interpret <b>Aramco project specifications, drawings, ITPs, and procedures</b> specific to civil engineering works.</li><li>Prepare, implement, and monitor the <b>Project Quality Plan (PQP)</b>, <b>Inspection and Test Plans (ITPs)</b>, and <b>Method Statements</b> for civil activities.</li><li>Conduct daily inspections and verification of <b>formwork, rebar, concrete works, backfilling, compaction, asphalt paving, waterproofing</b>, etc.</li><li>Monitor and control <b>concrete batching</b>, slump testing, cube testing, curing, etc., and ensure traceability.</li><li>Coordinate third-party and client inspections and ensure proper <b>Request for Inspection (RFI)</b> submissions with complete documentation.</li><li>Identify and report <b>non-conformities</b>, initiate <b>Corrective and Preventive Actions (CAPA)</b>, and verify closures.</li><li>Ensure proper material approvals and that all <b>civil materials</b> (e.g., cement, aggregates, rebar, waterproofing membranes, etc.) are <b>Aramco-approved</b> and tested per specifications.</li><li>Maintain QA/QC documentation: inspection records, NCR logs, material approvals, concrete test results, compaction tests, etc.</li><li>Conduct <b>internal audits</b> and ensure civil construction compliance with <b>ISO 9001</b>, Aramco <b>SAES-Q-001</b>, <b>SAES-A-112</b>, and relevant international codes (ACI, ASTM, BS, etc.).</li><li>Interface with <b>Aramco Civil QC Inspectors</b>, consultants, and internal site teams to resolve technical and quality issues.</li><li>Participate in <b>Pre-Inspection Meetings (PIMs)</b> and ensure quality deliverables are submitted for Aramco Mechanical Completion and Final Acceptance.</li><li>Support QA/QC Manager in ensuring all civil works pass <b>final inspections and handover</b> processes.</li></ul><p>Qualifications &amp; ExperienceCriteriaRequirement<b>Education</b>BSc / BEng in Civil Engineering (Mandatory)<b>Approval</b>Must be <b>Aramco-approved as a Civil QA/QC Engineer</b> (with SAP/ID approval number or via Aramco CBT / vendor portal)<b>Experience</b>5&ndash;10+ years in QA/QC Civil on Aramco or Oil &amp; Gas infrastructure projects in Saudi Arabia<b>Certifications</b>ISO 9001:2015 QMS (Lead Auditor is a plus); relevant civil inspection training; concrete or soil lab testing certificates (preferred)<b>Codes &amp; Standards</b>Deep knowledge of Aramco <b>SAES, SATIP, SAIC</b>, <b>ACI</b>, <b>ASTM</b>, <b>ACI 301/318</b>, <b>IBC</b>, <b>IBC</b>, <b>BS 8110</b>, etc.</p><p>Required Skills</p><ul><li>Attention to detail, analytical mindset</li><li>Strong knowledge of <b>construction materials testing</b> (soil, concrete, asphalt)</li><li>Good communication and report writing skills</li><li>Capable of interpreting technical drawings and specifications</li><li>Ability to manage documentation for audits and inspections</li><li>Experience using quality software tools or inspection systems (e.g., QMIS, Aramco SAP interface)</li></ul><p>Key Responsibilities &ndash; Specific ActivitiesActivityQA/QC Involvement<b>Excavation &amp; Backfilling</b>Verify approved soil, compaction tests (FDT, Proctor), layer thickness<b>Formwork &amp; Rebar</b>Check alignment, cover, tying, cleaning prior to pour<b>Concrete Works</b>Monitor pouring, slump, temperature, test cubes, curing methods<b>Asphalt Works</b>Ensure approved mix, compaction, density testing<b>Structural Works</b>Ensure compliance in alignment, bolting, grouting, etc.<b>Finishes &amp; Masonry</b>Ensure level/plumb, joints, curing, workmanship</p><p>Reporting &amp; Documentation</p><ul><li>Daily QC inspection reports</li><li>Non-Conformance Reports (NCRs)</li><li>Corrective &amp; Preventive Actions (CAPAs)</li><li>Materials approval submissions</li><li>Site testing logs and lab reports</li><li>Final dossier preparation for handover</li></ul><p>Job Type: Full-time</p><p>Pay: &#65020;5,000.00 - &#65020;6,000.00 per month</p>

QA/QC Civil Engineer (Aramco Approved)

HanmiGlobal Saudi

<p></p><div><p><b>Role Purpose</b></p><p>
The BIM Manager (PMC) is responsible for <b>overseeing the planning, implementation, and monitoring of BIM processes</b> across all project phases. to ensures that design consultants, contractors, and sub-consultants comply with BIM standards, that models are coordinated and clash-free, and that information deliverables are structured to support construction, operation, and facilities management in alignment with <b>ISO 19650</b> and Rua Al Harams strategic digital requirements.</p><p><b>
Key Responsibilities</b></p><p><b>
1. BIM Standards &amp; Governance</b></p><ul><li>
Ensure all stakeholders (design consultants, contractors, sub-consultants, vendors) comply with the project BIM scope and standards.</li><li>
Implement ISO 19650-compliant BIM processes.</li><li>
Review and approve BIM software platforms (Autodesk Suite, Navisworks, Civil 3D, etc.).</li><li>
Enforce model naming conventions, file exchange protocols, and project coding standards (WBS-based).</li></ul><p><b>
2. Model Development &amp; Information Management</b></p><ul><li>
Define and monitor progressive Levels of Development (LOD 100 500) across disciplines.</li><li>
Ensure design consultants deliver LOD 300 models and contractors progress to LOD 400/500.</li><li>
Review BIM models for data integrity, geometry accuracy, and alignment with project scope.</li><li>
Guarantee that BIM deliverables align with project scheduling, cost planning (5D), sustainability, and FM handover requirements.</li></ul><p><b>
3. Coordination &amp; Clash Detection</b></p><ul><li>
Lead the federation of architectural, structural, MEP, civil, infrastructure, and ID models.</li><li>
Perform regular clash detection and coordination sessions.</li><li>
Track and close out BIM-related RFIs, NCRs, and outstanding issues.</li><li>
Facilitate weekly BIM coordination meetings and issue logs.</li></ul><p><b>
4. QA/QC &amp; Risk Management</b></p><ul><li>
Establish and implement BIM QA/QC protocols and checklists.</li><li>
Audit model submissions and produce compliance review reports.</li><li>
Identify BIM-related risks and develop mitigation strategies.</li><li>
Ensure vendor and sub-consultant data is integrated into the master model.</li></ul><p><b>
5. Information Exchange &amp; CDE Management</b></p><ul><li>
Oversee Common Data Environment (CDE) setup, permissions, and workflows (e.g., ACC/BIM 360).</li><li>
Define data exchange formats (RVT, IFC, NWC, COBie).</li><li>
Ensure proper documentation of approvals, revisions, and handover packages.</li></ul><p><b>
6. Reporting &amp; Communication</b></p><ul><li>
Produce <b>monthly BIM reports and dashboards</b>, covering clash metrics, compliance, risks, and progress.</li><li>
Provide digital presentations and workshops to Rua and stakeholders on BIM progress and strategy.</li><li>
Act as the PMCs <b>BIM Champion</b>, liaising between Rua, design consultants, contractors, and FM teams.</li></ul><p><b>
7. Handover &amp; Asset Information Management</b></p><ul><li>
Define and enforce model handover protocols (design contractor operator).</li><li>
Ensure As-Built models are fully updated, validated, and FM-ready (including COBie or equivalent data).</li><li>
Support Rua in establishing a digital twin strategy for future operations.</li></ul><p><b>
Required Skills &amp; Competencies</b></p><ul><li>
Strong expertise in <b>BIM management for high-rise large-scale, multi-disciplinary projects</b> (architecture, structure, MEP, infrastructure, interiors).</li><li>
In-depth knowledge of <b>ISO 19650 standards</b>, PAS 1192, and best-practice BIM workflows.</li><li>
Proficiency in Autodesk Suite (Revit, Navisworks, Civil 3D), CDE platforms (ACC/BIM 360, Aconex), and BIM coordination tools (Solibri, BIM Track, etc.).</li><li>
Proven experience in clash detection, model auditing, and QA/QC.</li><li>
Ability to align BIM deliverables with <b>project controls, scheduling (4D), cost management (5D), and FM handover</b>.</li><li>
Strong leadership and stakeholder management skills.</li><li>
Excellent reporting, presentation, and communication abilities.</li><li>
Experience in the Middle East (preferred), particularly with <b>luxury residential, hospitality, or mixed-use developments</b>.</li></ul><p><b>
Qualifications</b></p><ul><li>
Bachelors degree in Architecture, Engineering, or Construction Management.</li><li>
Professional certification in BIM (e.g., Autodesk Certified Professional, BRE BIM ISO 19650 Practitioner, RICS BIM Manager).</li><li>
Minimum 15 years BIM experience, including <b>BIM Manager role for PMC </b>.</li><li>
Experience working with multidisciplinary teams and major international projects.</li></ul></div><p></p>

BIM Manager - MRF 25057

IVD Almubtakara Factory

<p><b>&#1575;&#1604;&#1605;&#1587;&#1605;&#1617;&#1609; &#1575;&#1604;&#1608;&#1592;&#1610;&#1601;&#1610;: &#1571;&#1582;&#1589;&#1575;&#1574;&#1610; &#1571;&#1606;&#1587;&#1580;&#1577;/&#1601;&#1606;&#1610; &#1573;&#1606;&#1578;&#1575;&#1580; &#1608;&#1605;&#1576;&#1610;&#1593;&#1575;&#1578;: &#1602;&#1587;&#1605; &#1593;&#1604;&#1605; &#1575;&#1604;&#1571;&#1605;&#1585;&#1575;&#1590; &#1575;&#1604;&#1606;&#1587;&#1610;&#1580;&#1610; (Histopathology)</b></p><p><b>Job Title: Histotechnologist &amp; Sales Specialist: Histopathology Production Line</b></p><p><b>&#1575;&#1604;&#1608;&#1592;&#1575;&#1574;&#1601; &#1608;&#1575;&#1604;&#1605;&#1587;&#1572;&#1608;&#1604;&#1610;&#1575;&#1578; (Roles &amp; Responsibilities)&#1571;&#1608;&#1604;&#1575;&#1611;: &#1603;&#1601;&#1606;&#1617;&#1610; &#1573;&#1606;&#1578;&#1575;&#1580; (As a Production Technologist)</b></p><ul><li>&#1578;&#1606;&#1601;&#1610;&#1584; &#1593;&#1605;&#1604;&#1610;&#1575;&#1578; &#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580; 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&#1608;&#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580; &#1576;&#1583;&#1602;&#1577; &#1608;&#1601;&#1602; &#1605;&#1605;&#1575;&#1585;&#1587;&#1575;&#1578; &#1575;&#1604;&#1578;&#1608;&#1579;&#1610;&#1602; &#1575;&#1604;&#1580;&#1610;&#1583; (GDP)&#1548; &#1608;&#1573;&#1580;&#1585;&#1575;&#1569; &#1575;&#1604;&#1601;&#1581;&#1608;&#1589;&#1575;&#1578; &#1571;&#1579;&#1606;&#1575;&#1569; &#1575;&#1604;&#1593;&#1605;&#1604;&#1610;&#1577; (&#1605;&#1579;&#1604; pH&#1548; &#1575;&#1604;&#1603;&#1579;&#1575;&#1601;&#1577;&#1548; &#1575;&#1604;&#1604;&#1586;&#1608;&#1580;&#1577;)&#1548; &#1608;&#1575;&#1604;&#1578;&#1606;&#1587;&#1610;&#1602; &#1605;&#1593; &#1571;&#1602;&#1587;&#1575;&#1605; &#1590;&#1605;&#1575;&#1606; &#1575;&#1604;&#1580;&#1608;&#1583;&#1577; &#1608;&#1605;&#1585;&#1575;&#1602;&#1576;&#1577; &#1575;&#1604;&#1580;&#1608;&#1583;&#1577; (QA/QC) &#1604;&#1604;&#1601;&#1581;&#1589; &#1608;&#1575;&#1604;&#1573;&#1591;&#1604;&#1575;&#1602; &#1608;&#1605;&#1593;&#1575;&#1604;&#1580;&#1577; &#1575;&#1604;&#1575;&#1606;&#1581;&#1585;&#1575;&#1601;&#1575;&#1578;.</li><li>&#1575;&#1604;&#1581;&#1601;&#1575;&#1592; &#1593;&#1604;&#1609; &#1580;&#1575;&#1607;&#1586;&#1610;&#1577; &#1605;&#1606;&#1591;&#1602;&#1577; &#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580; &#1608;&#1606;&#1592;&#1575;&#1601;&#1578;&#1607;&#1575; &#1608;&#1601;&#1602; &#1575;&#1604;&#1582;&#1591;&#1591; &#1575;&#1604;&#1605;&#1593;&#1578;&#1605;&#1583;&#1577;&#1548; &#1608;&#1575;&#1604;&#1575;&#1604;&#1578;&#1586;&#1575;&#1605; &#1576;&#1575;&#1585;&#1578;&#1583;&#1575;&#1569; &#1605;&#1593;&#1583;&#1575;&#1578; &#1575;&#1604;&#1608;&#1602;&#1575;&#1610;&#1577; &#1575;&#1604;&#1588;&#1582;&#1589;&#1610;&#1577; (PPE) &#1608;&#1575;&#1578;&#1576;&#1575;&#1593; &#1578;&#1593;&#1604;&#1610;&#1605;&#1575;&#1578; &#1606;&#1588;&#1585;&#1575;&#1578; &#1575;&#1604;&#1587;&#1604;&#1575;&#1605;&#1577; &#1575;&#1604;&#1603;&#1610;&#1605;&#1610;&#1575;&#1574;&#1610;&#1577; (MSDS)&#1548; &#1608;&#1590;&#1605;&#1575;&#1606; &#1575;&#1604;&#1575;&#1604;&#1578;&#1586;&#1575;&#1605; &#1576;&#1573;&#1580;&#1585;&#1575;&#1569;&#1575;&#1578; &#1575;&#1604;&#1587;&#1604;&#1575;&#1605;&#1577; &#1608;&#1575;&#1604;&#1589;&#1581;&#1577; &#1575;&#1604;&#1605;&#1607;&#1606;&#1610;&#1577; &#1608;&#1575;&#1604;&#1576;&#1610;&#1574;&#1577; &#1608;&#1575;&#1604;&#1578;&#1582;&#1604;&#1589; &#1575;&#1604;&#1570;&#1605;&#1606; &#1605;&#1606; &#1575;&#1604;&#1606;&#1601;&#1575;&#1610;&#1575;&#1578;.</li></ul><p>- Execute production and manufacturing processes in accordance with approved formulations, Standard Operating Procedures (SOPs), and the requirements of ISO 13485 and the Saudi Food and Drug Authority (SFDA).</p><p>- Contribute to the creation and revision of production procedures and related records, ensuring accuracy and compliance. Production activities include but are not limited to mixing, filling, capping, labeling, stacking, and final product handling to achieve high-quality output.</p><p>- Verify raw materials (batch numbers, expiry dates, certificates of analysis) and ensure calibration and functionality of production equipment (balances, pH meters, mixers, measuring tools).</p><p>- Record production data accurately following Good Documentation Practice (GDP), perform in-process quality checks (pH, density, viscosity), and coordinate with QA/QC for inspection, release, and deviation management.</p><p>- Maintain readiness and cleanliness of the production area as per the established housekeeping plan, comply with PPE requirements, follow Safety Data Sheet (SDS) instructions, and adhere to Health, Safety, and Environmental (HSE) procedures including waste management.</p><ul><li>&#1575;&#1604;&#1576;&#1581;&#1579; &#1593;&#1606; &#1593;&#1605;&#1604;&#1575;&#1569; &#1580;&#1583;&#1583; (&#1605;&#1587;&#1578;&#1588;&#1601;&#1610;&#1575;&#1578;&#1548; &#1605;&#1582;&#1578;&#1576;&#1585;&#1575;&#1578;&#1548; &#1605;&#1608;&#1586;&#1593;&#1608;&#1606;&#1548; &#1580;&#1575;&#1605;&#1593;&#1575;&#1578;...) &#1608;&#1575;&#1604;&#1581;&#1601;&#1575;&#1592; &#1593;&#1604;&#1609; &#1575;&#1604;&#1593;&#1604;&#1575;&#1602;&#1575;&#1578; &#1605;&#1593; &#1575;&#1604;&#1593;&#1605;&#1604;&#1575;&#1569; &#1575;&#1604;&#1581;&#1575;&#1604;&#1610;&#1610;&#1606; &#1605;&#1606; &#1582;&#1604;&#1575;&#1604; &#1575;&#1604;&#1586;&#1610;&#1575;&#1585;&#1575;&#1578; &#1575;&#1604;&#1605;&#1610;&#1583;&#1575;&#1606;&#1610;&#1577; &#1608;&#1575;&#1604;&#1593;&#1585;&#1608;&#1590; &#1575;&#1604;&#1578;&#1602;&#1583;&#1610;&#1605;&#1610;&#1577; &#1575;&#1604;&#1583;&#1608;&#1585;&#1610;&#1577;.</li><li>&#1573;&#1593;&#1583;&#1575;&#1583; &#1593;&#1585;&#1608;&#1590; &#1575;&#1604;&#1571;&#1587;&#1593;&#1575;&#1585; &#1576;&#1606;&#1575;&#1569;&#1611; &#1593;&#1604;&#1609; &#1578;&#1603;&#1575;&#1604;&#1610;&#1601; &#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580; &#1608;&#1607;&#1575;&#1605;&#1588; &#1575;&#1604;&#1585;&#1576;&#1581; &#1575;&#1604;&#1605;&#1593;&#1578;&#1605;&#1583;&#1548; &#1608;&#1605;&#1578;&#1575;&#1576;&#1593;&#1577; &#1571;&#1608;&#1575;&#1605;&#1585; &#1575;&#1604;&#1588;&#1585;&#1575;&#1569; &#1608;&#1575;&#1604;&#1578;&#1587;&#1604;&#1610;&#1605; &#1608;&#1575;&#1604;&#1601;&#1608;&#1575;&#1578;&#1610;&#1585; &#1581;&#1578;&#1609; &#1575;&#1604;&#1578;&#1581;&#1589;&#1610;&#1604; &#1575;&#1604;&#1606;&#1607;&#1575;&#1574;&#1610;.</li><li>&#1578;&#1602;&#1583;&#1610;&#1605; &#1588;&#1585;&#1608;&#1581;&#1575;&#1578; &#1601;&#1606;&#1610;&#1577; &#1571;&#1587;&#1575;&#1587;&#1610;&#1577; &#1604;&#1604;&#1593;&#1605;&#1604;&#1575;&#1569; &#1581;&#1608;&#1604; &#1575;&#1587;&#1578;&#1582;&#1583;&#1575;&#1605; &#1575;&#1604;&#1605;&#1606;&#1578;&#1580;&#1575;&#1578; &#1608;&#1578;&#1591;&#1576;&#1610;&#1602;&#1575;&#1578;&#1607;&#1575;&#1548; &#1608;&#1575;&#1604;&#1578;&#1593;&#1575;&#1605;&#1604; &#1605;&#1593; &#1575;&#1604;&#1605;&#1604;&#1575;&#1581;&#1592;&#1575;&#1578; &#1571;&#1608; &#1575;&#1604;&#1588;&#1603;&#1575;&#1608;&#1609; &#1575;&#1604;&#1601;&#1606;&#1610;&#1577; &#1576;&#1575;&#1604;&#1578;&#1606;&#1587;&#1610;&#1602; &#1605;&#1593; &#1602;&#1587;&#1605; &#1575;&#1604;&#1580;&#1608;&#1583;&#1577; &#1608;&#1585;&#1576;&#1591;&#1607;&#1575; &#1576;&#1606;&#1592;&#1575;&#1605; PMS/CAPA.</li><li>&#1580;&#1605;&#1593; &#1608;&#1578;&#1581;&#1604;&#1610;&#1604; &#1605;&#1604;&#1575;&#1581;&#1592;&#1575;&#1578; &#1575;&#1604;&#1587;&#1608;&#1602; &#1608;&#1575;&#1604;&#1605;&#1606;&#1575;&#1601;&#1587;&#1610;&#1606;&#1548; &#1608;&#1575;&#1604;&#1605;&#1588;&#1575;&#1585;&#1603;&#1577; &#1601;&#1610; &#1573;&#1593;&#1583;&#1575;&#1583; &#1575;&#1604;&#1605;&#1608;&#1575;&#1583; &#1575;&#1604;&#1578;&#1587;&#1608;&#1610;&#1602;&#1610;&#1577; (Datasheets / IFU / Catalogues) &#1608;&#1575;&#1604;&#1605;&#1587;&#1575;&#1607;&#1605;&#1577; &#1601;&#1610; &#1578;&#1591;&#1608;&#1610;&#1585; &#1575;&#1604;&#1605;&#1606;&#1578;&#1580;&#1575;&#1578; &#1608;&#1578;&#1581;&#1587;&#1610;&#1606; &#1582;&#1591;&#1591; &#1575;&#1604;&#1605;&#1576;&#1610;&#1593;&#1575;&#1578; &#1575;&#1604;&#1605;&#1587;&#1578;&#1602;&#1576;&#1604;&#1610;&#1577;.</li></ul><p>- Identify and develop new customer accounts (hospitals, laboratories, distributors, universities, etc.) while maintaining strong relationships with existing clients through regular visits and presentations.</p><p>- Prepare quotations based on production cost and target profit margins, and manage the full sales process &mdash; from purchase orders and delivery follow-up to invoicing and collection.</p><p>- Provide basic technical support and product guidance to customers, handle feedback and complaints, and ensure all are reported through the PMS/CAPA system in coordination with the Quality Department.</p><p>- Collect and analyze market and competitor information, contribute to the preparation of marketing materials (Datasheets / IFUs / Catalogues), and assist in product improvement and sales planning initiatives.</p><p>Job Type: Full-time</p><p>Ability to commute/relocate:</p><ul><li>Jeddah: Reliably commute or planning to relocate before starting work (Preferred)</li></ul><p>Application Question(s):</p><ul><li>Experienced in the preparation of routine histopathology products</li></ul><p>Education:</p><ul><li>Master's (Preferred)</li></ul><p>Language:</p><ul><li>English (Preferred)</li></ul><p>License/Certification:</p><ul><li>driving license (Preferred)</li></ul><p>Location:</p><ul><li>Jeddah (Preferred)</li></ul><p>Willingness to travel:</p><ul><li>25% (Preferred)</li></ul>

Histotechnologist / Histopathology Specialist

<div>
 <strong>
  Site Name:
 </strong>
 Saudi Arabia - Jeddah
 <br/>
 <br/>
 <strong>
  Posted Date:
 </strong>
 Oct 22 2025
 <br/>
 <br/>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
  <br/>
  <br/>
 </strong>
 Are you a
 <strong>
  Quality professional
 </strong>
 who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role
 <strong>
  QC Chemist
 </strong>
 is the one for you to explore.
 <br/>
 <br/>
 As
 <strong>
  QC Chemist
 </strong>
 you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements
 <br/>
 <br/>
 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Following all EHS guidelines in the analytical laboratory and on the entire facility
  </li>
  <li>
   Compliance with all GMP, QMS and data integrity requirements, as well as regulatory expectations.
  </li>
  <li>
   Perform the sampling activity for Microbiology, Materials and Finished goods, in compliance to GMP requirements.
  </li>
  <li>
   Perform the chemical and microbiological testing for stability samples, finished product and raw materials.
  </li>
  <li>
   Perform and execute the utilities and cross contamination testing plan.
  </li>
  <li>
   Test to be comply with local methods and specification as per SOP, BARs &amp; RMA or RMS methods.
  </li>
  <li>
   Preparation of all required documentation for testing, including BARs, stability protocols and reports.
  </li>
  <li>
   Preparation of all required reagents for testing.
  </li>
  <li>
   Perform calibration and maintenance of certain laboratory equipment as assigned.
  </li>
  <li>
   Inventory check and ordering of chemical and glassware as required.
  </li>
  <li>
   On time complete training curricula assigned in My-Learning or QMS training and provide the training to the staff where it is required.
  </li>
  <li>
   Maintain the Data record and entree in all QC related documents and files.
  </li>
  <li>
   Adhering to the OOS procedure and documenting investigations as required.
  </li>
  <li>
   To provide support to PPR by providing trend results for critical product (release) parameters, OOS investigation reports, providing laboratory equipment validation status and analytical method status.
  </li>
  <li>
   Identify any risk and escalate to the line manager, where applicable.
  </li>
  <li>
   Following and sustaining GPS standards for all lab activities.
  </li>
  <li>
   Supervisor, develop, implement and monitor chemical laboratory procedures (SOP/ BAR/ RMA/ BPS) against regulatory, QMS, CAPs and pharmacopoeia requirements, and ensuring compliance of laboratory activities with local SOPs. And provide the training to the analyst and technicians as required.
  </li>
  <li>
   Perform and supervisor analytical method validation or transfer as required, cleaning validation, analytical equipments validation (IQ, OQ &amp; PQ), Calibration and maintenance with related scheduled.
  </li>
  <li>
   Checking / verifying the entire chemical lab result and submit to QC manager for final approval, execute OOS investigations when required and ensure trending of critical product parameters are trended, reviewed and available for PPR.
  </li>
  <li>
   Maintain the Data record and entree in all QC related documents and files.
  </li>
  <li>
   Monitoring the lab inventory of the lab wear, consumables materials, chemicals and reference standard.
  </li>
  <li>
   Promote safe-working and laboratory environment that complies with company EHS requirements.
  </li>
  <li>
   Identify any risk and escalate to the line manager,
  </li>
  <li>
   Adhere to Safety, Quality and GPS standards and sustain the relevant QA &amp; EHS KPI metrics to achieve Zero Accident, Zero Defect, Zero Waste and continues improvements.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <em>
   Why you?
   <br/>
   <br/>
  </em>
 </strong>
 <strong>
  <em>
   Basic Qualifications:
   <br/>
   <br/>
  </em>
 </strong>
 We are looking for professionals with these required skills to achieve our goals:
 <br/>
 <br/>
 <br/>
 <ul>
  <li>
   Bachelor&rsquo;s degree with majors in Chemistry, Biochemistry or Pharmacy.
  </li>
  <li>
   2 - 4 years of experience in similar role.
  </li>
  <li>
   Good level of English in terms of speaking, writing and reading.
  </li>
  <li>
   Knowledge of EHS, GMP and GLP.
  </li>
  <li>
   Computer Skills (Word, Excel &amp; Power point).
  </li>
  <li>
   Time management skills.
  </li>
  <li>
   Good analytical and problem-solving skills.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why GSK?
  <br/>
  <br/>
  Uniting science, technology and talent to get ahead of disease together.
  <br/>
  <br/>
 </strong>
 GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
 <br/>
 <br/>
 People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
 <br/>
 <br/>
 <strong>
  Contact information:
  <br/>
  <br/>
 </strong>
 You may apply for this position online by selecting the
 <strong>
  Apply now
 </strong>
 button.
 <br/>
 <br/>
 <strong>
  Important notice to Employment businesses/ Agencies
  <br/>
  <br/>
 </strong>
 GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
</div>


QC Chemist

<div><b>Site Name:</b> Saudi Arabia - Jeddah<br>
<b>Posted Date:</b> Oct 22 2025<p><br>
Job Description</p><p><b>
GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.</b></p><p>
Are you a <b>Quality professional </b>who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role <b>QC Chemist </b>is the one for you to explore.</p><p>
As <b>QC Chemist</b> you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements</p><p><br>
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;</p><p><b>
Key Responsibilities
</b></p><ul><li>Following all EHS guidelines in the analytical laboratory and on the entire facility</li><li>
Compliance with all GMP, QMS and data integrity requirements, as well as regulatory expectations.</li><li>
Perform the sampling activity for Microbiology, Materials and Finished goods, in compliance to GMP requirements.</li><li>
Perform the chemical and microbiological testing for stability samples, finished product and raw materials.</li><li>
Perform and execute the utilities and cross contamination testing plan.</li><li>
Test to be comply with local methods and specification as per SOP, BARs &amp; RMA or RMS methods.</li><li>
Preparation of all required documentation for testing, including BARs, stability protocols and reports.</li><li>
Preparation of all required reagents for testing.</li><li>
Perform calibration and maintenance of certain laboratory equipment as assigned.</li><li>
Inventory check and ordering of chemical and glassware as required.</li><li>
On time complete training curricula assigned in My-Learning or QMS training and provide the training to the staff where it is required.</li><li>
Maintain the Data record and entree in all QC related documents and files.</li><li>
Adhering to the OOS procedure and documenting investigations as required.</li><li>
To provide support to PPR by providing trend results for critical product (release) parameters, OOS investigation reports, providing laboratory equipment validation status and analytical method status.</li><li>
Identify any risk and escalate to the line manager, where applicable.</li><li>
Following and sustaining GPS standards for all lab activities.</li><li>
Supervisor, develop, implement and monitor chemical laboratory procedures (SOP/ BAR/ RMA/ BPS) against regulatory, QMS, CAPs and pharmacopoeia requirements, and ensuring compliance of laboratory activities with local SOPs. And provide the training to the analyst and technicians as required.</li><li>
Perform and supervisor analytical method validation or transfer as required, cleaning validation, analytical equipments validation (IQ, OQ &amp; PQ), Calibration and maintenance with related scheduled.</li><li>
Checking / verifying the entire chemical lab result and submit to QC manager for final approval, execute OOS investigations when required and ensure trending of critical product parameters are trended, reviewed and available for PPR.</li><li>
Maintain the Data record and entree in all QC related documents and files.</li><li>
Monitoring the lab inventory of the lab wear, consumables materials, chemicals and reference standard.</li><li>
Promote safe-working and laboratory environment that complies with company EHS requirements.</li><li>
Identify any risk and escalate to the line manager,</li><li>
Adhere to Safety, Quality and GPS standards and sustain the relevant QA &amp; EHS KPI metrics to achieve Zero Accident, Zero Defect, Zero Waste and continues improvements.</li></ul><p><b><i>
Why you?</i></b></p><p><b><i>
Basic Qualifications:
</i></b></p><p>We are looking for professionals with these required skills to achieve our goals:</p><ul><li>
Bachelor&rsquo;s degree with majors in Chemistry, Biochemistry or Pharmacy.</li><li>
2 - 4 years of experience in similar role.</li><li>
Good level of English in terms of speaking, writing and reading.</li><li>
Knowledge of EHS, GMP and GLP.</li><li>
Computer Skills (Word, Excel &amp; Power point).</li><li>
Time management skills.</li><li>
Good analytical and problem-solving skills.</li></ul><p></p><p><b>
Why GSK?</b><br>
<b>Uniting science, technology and talent to get ahead of disease together.</b></p><p></p><p>
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.</p><p></p><p>
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><p><b>
Contact information:</b><br>
You may apply for this position online by selecting the <b>Apply now</b> button.</p><p></p><p><b>
Important notice to Employment businesses/ Agencies</b></p><p>
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p></div>

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next!<br>
<p></p>At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what&rsquo;s possible.<br>
<p></p><p><b>Job Description:
</b></p><p>Parsons is looking for an amazingly talented <b>Sr. Manager/Subject Matter Expert - QA/QC Lead </b>- to join our team. Provides senior-level management direction for the practice of quality, including administrative and supervisory responsibilities for one or more major project(s)/program(s) and/or functional areas to ensure that products or services provided are in accordance with customer and Parsons Quality requirements. This position offers strategic leadership in the development and implementation of regional or major project/program level Quality systems, procedures, and related quality activities. The role involves overseeing a team of Quality professionals, including ensuring continuous professional development. Regularly interacts with executive and senior-level representatives from a variety of functional groups within and across Business Units (BUs), including program/project management, safety, design/engineering, contracts, procurement, construction, and other personnel.
</p><p></p><p><b>What You'll Be Doing:
</b></p><ul><li>Participates in the interview and selection process (including hiring recommendations), and makes staffing assignments in accordance with schedule requirements.
</li><li>Conducts performance evaluations and makes appropriate recommendations for required actions, including recommendations for advancement, changes in status, or disciplinary action.
</li><li>Manages the salary administration process, including preparing the annual salary plan and recommending salary actions for merit increases and/or promotions.
</li><li>Provides Quality Systems management using the Parsons Quality Management System as the basis for process development and optimization, procedure development, data collection and reporting and Quality Systems training.
</li><li>Oversees efforts to maintain Parsons quality-related certifications.
</li><li>Interfaces at senior and executive levels with regard to quality process improvement and re-engineering.
</li><li>Participates in Client pre-bid, bid or contract planning and preparation.
</li><li>Establishes project/program Quality Systems and audits schedules, conducts audits, and facilitates corrective actions.
</li><li>Performs independent audits in various areas and ensures compliance with QA/QC programs.
</li><li>Reviews documents, witnesses audited activities, prepares checklists, performs audits, and prepares final reports.
</li><li>Analyzes audit findings to determine program quality and identify trends.
</li><li>Promotes a uniform Corrective Action/Preventive Action and Non-conformance tracking program.
</li><li>Ensures compliance with Parsons&rsquo; and Client quality requirements.
</li><li>Verifies that Parsons and customers&rsquo; quality requirements are in compliance with quality standards and quality program requirements for products and services provided.
</li><li>Develops and maintains project/program Quality Procedures and related documents (or oversee same).
</li><li>Reviews Quality Manuals, documents, and implementation procedures to verify compliance with industry codes and standards, regulations and regulatory commitments.
</li><li>Reviews from a quality perspective (and approves if required) documents prepared by internal or external organizations such as quality manuals and procedures, technical deliverables, test plans and procedures, purchase orders, and subcontracts.
</li><li>Facilitates project/program staffing.
</li><li>Collaborates with management for quality activities with internal or external interfaces.
</li><li>Handles in qualification audits of suppliers of purchased items and services.
</li><li>Supports development and maintenance of corporate quality governance, as requested.
</li><li>Provides technical guidance to lower level Quality personnel, as needed.
</li><li>Performs other responsibilities associated with this position as may be appropriate.
</li></ul><p></p><p><b>What Required Skills You&rsquo;ll Bring
</b></p><ul><li>Bachelor's degree in Engineering, Construction Management or a related field.
</li><li>Minimum of 20 years of experience on a major Projects/Programs, with at least 10 years in a management or leadership role.
</li><li>Requires expert management ability and extensive knowledge of Quality
</li><li>Management practices, processes and current technology
</li><li>Requires thorough experience in directing and implementing quality management systems and standards specified by ISO 9000, ASME, ANSI, ASTM and similar organizations
</li><li>Clear communication, presentation, and interpersonal skills
</li><li>Ability to analyze business situations (ROI, cost per unit)
</li><li>Effective written, verbal, analytical, problem-solving, and risk assessment skills. Ability to make public presentations
</li><li>Proficiency in Microsoft Office (Word, Excel, PowerPoint)
</li><li>Attention to detail
</li><li>Expert working knowledge of ISO Quality Management Systems Standards
</li><li>Ability to direct and manage team members with day to day quality activities as well as special projects to assure timely completion
</li><li>Possesses working knowledge of more than one area of industry such as infrastructure, government, aviation, process, or transportation
</li><li>Certified ISO-9000 Lead Auditor Lead Auditor certification (ISO 9001 or equal), or ability to obtain within 6-months of hire.
</li><li>ASQ Certified Quality Engineer. or ability to obtain within 6-months of hire.
</li><li>Other related certification(s) (e.g. CMQ/OE, CQA, or CQE).
</li><li>(Preferred) Membership in a nationally-recognized Quality organization.
</li></ul><p></p>Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
<p></p><p>We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!
</p><p></p><p>Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/ .</p></div>

Sr. Manager/Subject Matter Expert - QA/QC Lead

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Histotechnologist / Histopathology Specialist

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Sr. Manager/Subject Matter Expert - QA/QC Lead