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customer experience specialist, sales - jeddah

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site quality manager saudi

Proterial

<div>Location:
Jeddah, Maddinah, Saudi Arabia
Job ID:
R0107655
Date Posted:
2025-10-14
Company Name:
HITACHI ENERGY LTD
Profession (Job Category):
Quality Management
Job Schedule:
Full time
Remote:
No
Job Description:
The opportunity
Plan, organize, lead and monitor all Quality work during site execution to ensure we satisfy customer expectations. This includes works undertaken internally in addition to the work performed by our subcontractors and/or partners as required for the project. The Site Quality Manager reports functionally to the Global Manager for Site Quality. During site execution the SQM reports operationally to the Site Manager and dotted to the PQM. 
 
How you&rsquo;ll make an impact
<ul><li>Review of contractual and local requirements applicable to site quality.
</li><li>Review lessons learnt from previous projects and relevant project plans (e.g SQP, SMP)
</li><li>Review Contractor Quality Plans to ensure alignment with the Project Quality Plans and the customer requirements.
</li><li>Based on reviews and discussion with stakeholders identify and follow up risks and mitigations to ensure we fulfill site quality expectations.
</li><li>Set up and educate site personnel in the quality management system including the completion system at site. Site Quality Execution Process.
</li><li>Provide Quality Induction training to the site personnel.
</li><li>Execute and follows up the Quality Plans, master test plan and completion system status for site activities as required.
</li><li>Review quality documentation for correctness and completeness prior approval (e.g. test certificates, checklist, etc.).
</li><li>Ensure that the quality control plans (ITP, ITR etc) and any erection documentation (Drawings, procedures, etc.) provided by HVDC are effectively communicated to the site management team and the contractors.
</li><li>Ensure that Quality Control processes are fully implemented and continuously monitored.
</li><li>Ensure that inspection / testing during Civil, Mechanical &amp; Electrical erection and Commissioning are con-ducted, documented, checked and validated as per the quality control system.
</li><li>If required support the Organization and supervision acceptance testing and/or approval by customers, third parties and governmental authorities whenever required at site.
</li><li>Ensure that the completion system, deviation, NCR (Non-Conformance Report) System, CCRP system and any other Quality tools are fully deployed at site and that the users are adequately trained with the support of the completion manager.
</li><li>Ensure that all testing and measurement equipment used at site are listed and calibrated and that the associated calibration certificates are available.
</li><li>Follow up completion system at site having an overview of status in regard to inspections, certifications and all outstanding works including punch list.
</li><li>Provide Quality related site KPIs to the stakeholders whenever required and follow-up onsite inspections and support the management of punch-out items.
</li><li>Provide Quality inputs to the site management to support on-time and in-budget execution of the project.
</li><li>If Required support the performance of Incoming inspection of goods at site and report any deviations according to the project regulations.
</li><li>Follows up that handling, storage of delivered material and equipment are in accordance with the manufacture&rsquo;s guidelines.
</li><li>Ensures that the ITP/ITR are applied by the sub-contractor and its subcontractors including the compliance with the Hold points and Witness points.
</li><li>Ensure site quality documentation is generated, distributed, updated and archived in accordance with the Management system and completion system requirements.
</li><li>Support the Deployment of Site Quality audit program (including contractor audits and internal audits).
</li><li>Participate in internal and contractor quality audits as per the Site Quality audit program.
</li><li>Assist and coordinate any planned external site related audits.
</li><li>Monitor contractor compliance with Quality requirements and follow up contractor corrective actions when-ever required.
</li><li>Follow up the adherence and governance of the quality management system at site.
</li><li>Support CoQP reporting processes at site according to HVDC processes.
</li><li>Support in identifying lessons learnt.
</li><li>Responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.
</li><li>Living Hitachi Energy core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business.
</li></ul>Your background
<ul><li>Technical / engineering / quality management education &ndash; minimum bachelor&rsquo;s degree.
</li><li>5+ year construction quality site experience or in operations.
</li><li>Power or energy industry experience.
</li><li>Track record and proven capability in Change Management, managing internal project/program in large and complex organization.
</li><li>Experience in process management ideally in project business, preferably in the energy or automation industry, or other quality and process-oriented industries.
</li><li>Continuous Improvement experience and L6S Belt.
</li><li>Capacity to communicate, result oriented, speed in execution, openness and listen to others.
</li><li>Test coordination experience.ISO9001 knowledge.
</li><li>Certified auditor. Knowledge and experience on construction codes / standards.
</li><li>Willing to be relocated to the project site location.
</li><li>Computer skills and knowledge of completion systems.
</li><li>Proficiency in both spoken &amp; written English language is required.
</li></ul><h2 class="jobSectionHeader">Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.
</h2><h2 class="jobSectionHeader">This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.</h2></div>

Site Quality Manager Saudi

Hitachi Energy

<div>Description
The opportunity
Plan, organize, lead and monitor all Quality work during site execution to ensure we satisfy customer expectations. This includes works undertaken internally in addition to the work performed by our subcontractors and/or partners as required for the project. The Site Quality Manager reports functionally to the Global Manager for Site Quality. During site execution the SQM reports operationally to the Site Manager and dotted to the PQM. 
How you&rsquo;ll make an impact<ul><li>
Review of contractual and local requirements applicable to site quality.</li><li>
Review lessons learnt from previous projects and relevant project plans (e.g SQP, SMP)</li><li>
Review Contractor Quality Plans to ensure alignment with the Project Quality Plans and the customer requirements.</li><li>
Based on reviews and discussion with stakeholders identify and follow up risks and mitigations to ensure we fulfill site quality expectations.</li><li>
Set up and educate site personnel in the quality management system including the completion system at site. Site Quality Execution Process.</li><li>
Provide Quality Induction training to the site personnel.</li><li>
Execute and follows up the Quality Plans, master test plan and completion system status for site activities as required.</li><li>
Review quality documentation for correctness and completeness prior approval (e.g. test certificates, checklist, etc.).</li><li>
Ensure that the quality control plans (ITP, ITR etc) and any erection documentation (Drawings, procedures, etc.) provided by HVDC are effectively communicated to the site management team and the contractors.</li><li>
Ensure that Quality Control processes are fully implemented and continuously monitored.</li><li>
Ensure that inspection / testing during Civil, Mechanical &amp; Electrical erection and Commissioning are con-ducted, documented, checked and validated as per the quality control system.</li><li>
If required support the Organization and supervision acceptance testing and/or approval by customers, third parties and governmental authorities whenever required at site.</li><li>
Ensure that the completion system, deviation, NCR (Non-Conformance Report) System, CCRP system and any other Quality tools are fully deployed at site and that the users are adequately trained with the support of the completion manager.</li><li>
Ensure that all testing and measurement equipment used at site are listed and calibrated and that the associated calibration certificates are available.</li><li>
Follow up completion system at site having an overview of status in regard to inspections, certifications and all outstanding works including punch list.</li><li>
Provide Quality related site KPIs to the stakeholders whenever required and follow-up onsite inspections and support the management of punch-out items.</li><li>
Provide Quality inputs to the site management to support on-time and in-budget execution of the project.</li><li>
If Required support the performance of Incoming inspection of goods at site and report any deviations according to the project regulations.</li><li>
Follows up that handling, storage of delivered material and equipment are in accordance with the manufacture&rsquo;s guidelines.</li><li>
Ensures that the ITP/ITR are applied by the sub-contractor and its subcontractors including the compliance with the Hold points and Witness points.</li><li>
Ensure site quality documentation is generated, distributed, updated and archived in accordance with the Management system and completion system requirements.</li><li>
Support the Deployment of Site Quality audit program (including contractor audits and internal audits).</li><li>
Participate in internal and contractor quality audits as per the Site Quality audit program.</li><li>
Assist and coordinate any planned external site related audits.</li><li>
Monitor contractor compliance with Quality requirements and follow up contractor corrective actions when-ever required.</li><li>
Follow up the adherence and governance of the quality management system at site.</li><li>
Support CoQP reporting processes at site according to HVDC processes.</li><li>
Support in identifying lessons learnt.</li><li>
Responsible for ensuring compliance with applicable external and internal regulations, procedures, and guidelines.</li><li>
Living Hitachi Energy core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business.</li></ul>
Your background<ul><li>
Technical / engineering / quality management education &ndash; minimum bachelor&rsquo;s degree.</li><li>
5+ year construction quality site experience or in operations.</li><li>
Power or energy industry experience.</li><li>
Track record and proven capability in Change Management, managing internal project/program in large and complex organization.</li><li>
Experience in process management ideally in project business, preferably in the energy or automation industry, or other quality and process-oriented industries.</li><li>
Continuous Improvement experience and L6S Belt.</li><li>
Capacity to communicate, result oriented, speed in execution, openness and listen to others.</li><li>
Test coordination experience.ISO9001 knowledge.</li><li>
Certified auditor. Knowledge and experience on construction codes / standards.</li><li>
Willing to be relocated to the project site location.</li><li>
Computer skills and knowledge of completion systems.</li><li>
Proficiency in both spoken &amp; written English language is required.</li></ul><h2 class="jobSectionHeader">
Qualified individuals with a disability may request a reasonable accommodation if you are unable or limited in your ability to use or access the Hitachi Energy career site as a result of your disability. You may request reasonable accommodations by completing a general inquiry form on our website. Please include your contact information and specific details about your required accommodation to support you during the job application process.</h2><h2 class="jobSectionHeader">
This is solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes will not receive a response.</h2></div>

Electrical Construction ManagerLocation: Jeddah, Saudi Arabia Experience Required: Minimum 15 years Industry: Construction / Infrastructure / MEPAbout the Role:We are seeking a highly experienced Electrical Construction Manager to lead and oversee all electrical works for major construction projects in Jeddah. The ideal candidate will have extensive experience managing large-scale infrastructure, commercial, or industrial projects &mdash; ensuring quality, safety, and timely completion.Key Responsibilities:<ul><li>Manage and supervise all on-site electrical construction activities.</li><li>Plan, schedule, and coordinate project timelines and resources.</li><li>Ensure all works comply with project specifications, standards, and safety regulations.</li><li>Review technical drawings, designs, and specifications.</li><li>Coordinate with other engineering disciplines (civil, mechanical, architectural, etc.).</li><li>Manage subcontractors, materials procurement, and quality control.</li><li>Monitor project budgets, progress, and prepare reports for senior management.</li><li>Provide leadership to project teams, ensuring productivity and safety compliance.</li></ul>Qualifications &amp; Experience:<ul><li>Bachelor&rsquo;s Degree in Electrical Engineering or related field (Master&rsquo;s preferred).</li><li>Minimum 15 years of experience in electrical construction within the building or infrastructure sector.</li><li>Proven experience managing large-scale projects in Saudi Arabia or the GCC region.</li><li>Strong knowledge of Saudi Building Codes and relevant electrical standards.</li><li>Excellent leadership, communication, and project management skills.</li><li>Proficiency in project management software (Primavera, MS Project, AutoCAD, etc.).</li><li>Fluent in English (Arabic an advantage).</li></ul>&quot;We require you to answer the screening questions&quot;All the best!Job Type: Full-timeApplication Question(s):<ul><li>What is your notice period?</li><li>Expected Salary as total package?</li><li>Are you willing to Relocate?</li></ul>Experience:<ul><li>Electrical Construction Manager: 10 years (Required)</li></ul>

Electrical Construction Manager (Construction Industry)

Analytix Arabia Management Consultant pvt ltd

Job Title: Audit Manager Location: Saudi Arabia Employment Type: Full-time, PermanentPosition Overview: We are seeking a highly skilled and experienced Audit Manager to lead comprehensive audit engagements, ensuring strict adherence to Saudi Arabian accounting and auditing standards. The successful candidate will oversee all audit operations, provide strategic insights to clients, and drive the growth and performance of a dedicated audit team.Key Responsibilities:<ul><li>Lead the planning, execution, and delivery of financial audits in compliance with local regulations and international best practices.</li><li>Perform thorough risk assessments, audit testing, and analytical reviews to detect potential discrepancies or areas of concern.</li><li>Prepare and deliver clear, concise audit reports outlining key findings and actionable recommendations.</li><li>Ensure full compliance with Saudi Arabian accounting and auditing standards throughout all audit processes.</li><li>Stay updated on changes in regulatory requirements and industry developments to uphold audit quality and compliance.</li><li>Advise clients on financial reporting, regulatory adherence, and operational enhancements.</li><li>Build and maintain strong, trust-based relationships with clients to foster long-term partnerships.</li><li>Effectively communicate audit outcomes and recommendations to clients and relevant stakeholders.</li><li>Mentor and supervise junior auditors, encouraging their professional development and ensuring high-quality work.</li><li>Collaborate with internal teams to guarantee timely and efficient completion of audits.</li><li>Support knowledge-sharing initiatives to promote continuous learning and improvement within the audit function.</li></ul>Qualifications:<ul><li>Chartered Accountant (CA) certification is mandatory.</li><li>3 to 5 years of relevant audit experience, preferably within Saudi Arabia.</li><li>In-depth knowledge of Saudi accounting and auditing standards.</li><li>Strong leadership, analytical, and communication skills.</li><li>Demonstrated ability to manage multiple audit engagements simultaneously while maintaining excellence.</li><li>Willingness and eligibility to relocate to Saudi Arabia.</li></ul>Job Type: Full-time

Audit Manager

<div>
 
 Site Name:
 
 Saudi Arabia - Jeddah
 
 
 
 Posted Date:
 
 Oct 22 2025
 
 
 
 Job Description
 
 
 
 
 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.
 
 
 
 Are you a
 
 Quality professional
 
 who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role
 
 QC Chemist
 
 is the one for you to explore.
 
 
 As
 
 QC Chemist
 
 you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements
 
 
 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
 
 
 
 Key Responsibilities
 
 
 
 
 <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>
 
 
 Why you?
 
 
 
 
 
 
 Basic Qualifications:
 
 
 
 
 We are looking for professionals with these required skills to achieve our goals:
 
 
 
 <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>
 
 Why GSK?
 
 
 Uniting science, technology and talent to get ahead of disease together.
 
 
 
 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.
 
 
 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.
 
 
 
 Contact information:
 
 
 
 You may apply for this position online by selecting the
 
 Apply now
 
 button.
 
 
 
 Important notice to Employment businesses/ Agencies
 
 
 
 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>Site Name: Saudi Arabia - Jeddah 
Posted Date: Oct 22 2025 
Job Description
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.
Are you a Quality professional who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role QC Chemist is the one for you to explore.
As QC Chemist you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements 
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
Key Responsibilities
<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>
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:<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>
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
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.
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.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
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>

COENGR - Consulting Engineering Group

The Role
 Senior Civil Engineer (Construction Manager) – Jeddah, KSA Location: Jeddah, Saudi Arabia Company: COENGR (Consulting Engineering /group) Position: Senior Civil Engineer / Construction Manager Availability: Immediate joiner required Key Responsibilities: • Oversee and manage all on-site civil construction activities. • Plan, schedule, and monitor project progress to ensure timely execution. • Coordinate with contractors, consultants, subcontractors, and client representatives. • Review engineering drawings, work methods, and material submittals. • Verify that construction activities comply with approved drawings, specifications, and authority standards. • Ensure compliance with quality, safety, and project specifications and as per LAWS. • Prepare daily/weekly reports and manage site staff performance. • Maintain clear communication between the site team and the design/office team.
 
Requirements
 <ul>
<li>Bachelor’s degree in Civil Engineering (Master’s preferred). • 4+ years of experience in large-scale construction projects (GCC/KSA experience preferred). • Strong leadership, planning, and site management capabilities. • Excellent knowledge of project execution, budgeting, and safety standards. • Immediate availability for relocation/joining in Jeddah.</li>
</ul>
About the company
 About COENGR: In the year 1976, Consulting engineering Group CEG was established in the Emirate of Ras Al Khaimah. CEG has built a reputation and image in delivering the designs. Today, we proudly introduce ourselves as a leading consulting firm in the Emirate of Ras Al khaimah having 30 years of experience in our record. With five offices in the cities of Ras Al Khaimah, Abu Dhabi, Dubai, Alain, and Ajman Our Staff exceeds 100 experienced and qualified engineers in many fields. Our company deals with different projects such as commercial, retail, industrial, sports facilities, resorts, hotels, and residential projects. We believe our success is largely due to our unwavering commitment to provide our clients and our team with their own unique opportunities to thrive. We do this by ensuring that our clients expectations and needs are our priorities and we provide our professionals with continual opportunities for development. Our roots are important to us. As we evolve and grow, we understand that maintaining the integrity of our past through a commitment to quality service, team member appreciation, and delivering innovative, practical solutions to our clients is the key to our success. Vision: To provide consultancy service that exceed our clients expectations, and to be widely recognized for our continuing commitment to client satisfaction. Mission: To deliver world-class engineering consultancy services while upholding higher quality and ethical standards. Values: At COENGR, we are committed to upholding the highest standards through our core values of Excellence, Integrity, and Quality in everything we do. We strive to deliver effcient and sustainable engineering solutions that not only meet client expectations but also contribute positively to the environment and community. Our workplace cultureis grounded in Mutual Respect, where every individual is valued, and collaboration is encouraged to promote a Cooperative Team Environment. By prioritizing Safety in all our operations and maintaining a strong ethical foundation, we ensure a reliable, responsible, and forward-thinking approach to every project.

Senior Civil Engineer

Explore 441+ Site quality manager saudi in Jeddah Saudi Arabia this November. Find roles across top companies and apply now to boost your career.

441 site quality manager saudi jobs IN Jeddah Saudi Arabia

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QC Chemist

Senior Civil Engineer