lab supervisor - gf Jobs in Jeddah Saudi Arabia

lab supervisor - gf

qa/qc architect Jobs in Jeddah Saudi Arabia

qa/qc architect

sr. manager/subject matter expert - qa/qc lead Jobs in Jeddah Saudi Arabia

sr. manager/subject matter expert - qa/qc lead

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>

QC Chemist

<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>


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

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; &#1608;&#1575;&#1604;&#1578;&#1589;&#1606;&#1610;&#1593; &#1608;&#1601;&#1602; &#1575;&#1604;&#1589;&#1610;&#1594; &#1575;&#1604;&#1605;&#1593;&#1578;&#1605;&#1583;&#1577; &#1608;&#1573;&#1580;&#1585;&#1575;&#1569;&#1575;&#1578; &#1575;&#1604;&#1578;&#1588;&#1594;&#1610;&#1604; &#1575;&#1604;&#1602;&#1610;&#1575;&#1587;&#1610;&#1577; (SOPs) &#1608;&#1605;&#1578;&#1591;&#1604;&#1576;&#1575;&#1578; &#1606;&#1592;&#1575;&#1605; &#1573;&#1583;&#1575;&#1585;&#1577; &#1575;&#1604;&#1580;&#1608;&#1583;&#1577; ISO 13485 &#1608;&#1604;&#1608;&#1575;&#1574;&#1581; &#1607;&#1610;&#1574;&#1577; &#1575;&#1604;&#1594;&#1584;&#1575;&#1569; &#1608;&#1575;&#1604;&#1583;&#1608;&#1575;&#1569; &#1575;&#1604;&#1587;&#1593;&#1608;&#1583;&#1610;&#1577; (SFDA).</li><li>&#1575;&#1604;&#1605;&#1587;&#1575;&#1607;&#1605;&#1577; &#1601;&#1610; &#1573;&#1606;&#1588;&#1575;&#1569; &#1608;&#1578;&#1593;&#1583;&#1610;&#1604; &#1605;&#1604;&#1601;&#1575;&#1578; &#1573;&#1580;&#1585;&#1575;&#1569;&#1575;&#1578; &#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580; &#1608;&#1605;&#1604;&#1581;&#1602;&#1575;&#1578;&#1607;&#1575; &#1605;&#1593; &#1590;&#1605;&#1575;&#1606; &#1575;&#1604;&#1583;&#1602;&#1577; &#1608;&#1575;&#1604;&#1575;&#1604;&#1578;&#1586;&#1575;&#1605;. &#1578;&#1588;&#1605;&#1604; &#1593;&#1605;&#1604;&#1610;&#1575;&#1578; &#1575;&#1604;&#1573;&#1606;&#1578;&#1575;&#1580;: &#1575;&#1604;&#1582;&#1604;&#1591;&#1548; &#1575;&#1604;&#1578;&#1593;&#1576;&#1574;&#1577;&#1548; &#1575;&#1604;&#1578;&#1594;&#1591;&#1610;&#1577;&#1548; &#1575;&#1604;&#1578;&#1603;&#1583;&#1610;&#1587;&#1548; &#1608;&#1608;&#1590;&#1593; &#1575;&#1604;&#1605;&#1604;&#1589;&#1602;&#1575;&#1578;&#1548; &#1604;&#1604;&#1581;&#1589;&#1608;&#1604; &#1593;&#1604;&#1609; &#1605;&#1606;&#1578;&#1580; &#1606;&#1607;&#1575;&#1574;&#1610; &#1605;&#1591;&#1575;&#1576;&#1602; &#1604;&#1604;&#1605;&#1608;&#1575;&#1589;&#1601;&#1575;&#1578;.</li><li>&#1575;&#1604;&#1578;&#1581;&#1602;&#1602; &#1605;&#1606; &#1575;&#1604;&#1605;&#1608;&#1575;&#1583; &#1575;&#1604;&#1582;&#1575;&#1605; (&#1571;&#1585;&#1602;&#1575;&#1605; &#1575;&#1604;&#1578;&#1588;&#1594;&#1610;&#1604;&#1575;&#1578;&#1548; &#1578;&#1608;&#1575;&#1585;&#1610;&#1582; &#1575;&#1604;&#1575;&#1606;&#1578;&#1607;&#1575;&#1569;&#1548; &#1588;&#1607;&#1575;&#1583;&#1575;&#1578; &#1575;&#1604;&#1578;&#1581;&#1604;&#1610;&#1604;...) &#1608;&#1590;&#1605;&#1575;&#1606; &#1605;&#1593;&#1575;&#1610;&#1585;&#1577; &#1608;&#1589;&#1604;&#1575;&#1581;&#1610;&#1577; &#1575;&#1604;&#1571;&#1580;&#1607;&#1586;&#1577; &#1575;&#1604;&#1605;&#1587;&#1578;&#1582;&#1583;&#1605;&#1577; (&#1575;&#1604;&#1605;&#1608;&#1575;&#1586;&#1610;&#1606;&#1548; &#1571;&#1580;&#1607;&#1586;&#1577; &#1602;&#1610;&#1575;&#1587; pH&#1548; &#1575;&#1604;&#1582;&#1604;&#1575;&#1591;&#1575;&#1578;&#1548; &#1608;&#1571;&#1583;&#1608;&#1575;&#1578; &#1575;&#1604;&#1601;&#1581;&#1589;).</li><li>&#1578;&#1587;&#1580;&#1610;&#1604; &#1580;&#1605;&#1610;&#1593; &#1576;&#1610;&#1575;&#1606;&#1575;&#1578; &#1575;&#1604;&#1578;&#1588;&#1594;&#1610;&#1604; &#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

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

Fosroc

<div><div><div><h3 class="jobSectionHeader"><b>Vacancy</b></h3></div><div><div><div><div><b>
Job title</b></div><div> Production Planner</div></div><br>
<div><div><b>
Department</b></div><div> Manufacturing</div></div><br>
<div><div><b>
Close date</b></div><div> 6th Nov 2025</div></div><br>
<div><div><b>
Location</b></div><div> Jeddah</div></div><div></div><div><div><b><br>
</b></div></div><br>
</div></div></div><div></div><div><div><h3 class="jobSectionHeader"><b>
Job description</b></h3></div><div><div><div><div><b>
Job description</b></div><div><li>Optimize resources and the scheduling of resources to meet production demand.
</li><br>
<li>Maintain planning and scheduling horizons to ensure visibility to all production stakeholders i.e., customer service, sales and supply chain functions.</li></div></div><br>
<div><div><b>
Responsibilities</b></div><div><li>Coordinating planning activities with Customer Service representatives, Sales team, and Supply chain to ensure that products are manufactured on given time to meet Customer requirements
</li><br>
<li>Ensure that committed production quantities are delivered on time and in full.
</li><br>
<li>Attend the daily demand meeting to update the CSD and sales on the production plan.
</li><br>
<li>Work with the materials planner to ensure that all raw materials are available for production to avoid production delays or disruption due to non-availability of raw materials.
</li><br>
<li>Ensure timely update of production orders on ERP to minimize variances and enhance supply chain material planning efforts.
</li><br>
<li>Use the sales forecast to prepare a long horizon production plan.
</li><br>
<li>Implement manufacturing strategy for planning of products based on their planning key
</li><br>
<li>(Critical, High, Medium, Low)
</li><br>
<li>Monitor and consider on-hand stocks of finished goods and raw materials while planning.
</li><br>
<li>Liaise with the maintenance planner to include the monthly preventive maintenance in the production schedule.
</li><br>
<li>Monitor the daily productivity and report any issues.
</li><br>
<li>Attend to actions related to slow or non-moving items.
</li><br>
<li>Improve M-OTIF, Monitor OEE and utilization per line &amp; per station, monitor forecast accuracy and its impact on planning.
</li><br>
<li>Improve reworks of non-confirming products.
</li><br>
<li>Monitor and coordinate with supervisors to improve material usage variance (MUV)
</li><br>
<li>Follow-up of work orders from production cells and QC.
</li><br>
<li>Set self as an example to colleagues in punctuality, commitment, respect to work hours, and dedication.
</li><br>
<li>Carry over additional duties as assigned by the Production Manager or Operations Manager.</li></div></div><br>
<div><div><b>
Skills required</b></div><div> Essential:
<br>
Fluent in English
<br>
Excellent communication skills
<br>
Interpersonal and leadership skills
<br>
5 years&rsquo; experience in production planning
<br>
<br>
Desirable:
<br>
Project management background or experience is a plus
<br>
Arabic speaking
<br>
Saudi national
<br>
Experience on production shopfloor in chemical industries.
<br>
Experience in S&amp;OP planning</div></div><br>
<div><div><b>
Educational requirements</b></div><div> BSc degree in industrial engineering, manufacturing</div></div><br>
<div><div><b>
Job role notes</b></div><div> Key Working Relationships:
<br>
Internal:
<br>
Production Planner (Daily)
<br>
Production Manager (Daily)
<br>
Operations Manager (Regular)
<br>
CSD team (Daily)
<br>
Maintenance planner (Regular)
<br>
Material Planner (Daily)
<br>
Operations Staff (Daily)
<br>
Technical Staff (Regular)
<br>
HSE team (Regular)
<br>
<br>
External:
<br>
Visitors (as needed)</div></div></div></div></div></div>

Production Planner

Rawafid

<div><p>Rawafid is seeking a talented and detail-oriented Electrical Draftsman to join our engineering team. In this role, you will be responsible for producing accurate and comprehensive electrical drawings and plans for various construction projects. Working closely with engineers and project managers, you will interpret design specifications and create detailed schematics, wiring diagrams, and layout plans. Your expertise in drafting techniques and electrical systems will play a critical role in ensuring that projects meet all relevant standards and requirements. If you have a strong background in electrical drafting and a commitment to quality, we welcome your application to become a valued member of the Rawafid team.</p><p></p><h3 class="jobSectionHeader"><b>
Key Responsibilities</b></h3><ul>
<li>Prepare drawing transmittals, revision logs, and drawing issue registers for submission to consultants and clients.</li>
<li>Coordinate with electrical engineers, mechanical draftsmen, and civil teams to ensure drawings are fully integrated and free of clashes</li>
<li>Participate in technical coordination meetings to resolve drawing and interface issues.</li>
<li>Maintain organized documentation of all drafts, revisions, and project files, ensuring proper version control.</li>
<li>Prepare single-line diagrams (SLDs), load schedules, cable schedules, and schematic diagrams for LV and MV systems.</li>
<li>Produce shop drawings and as-built drawings in coordination with site teams and consultants.</li>
<li>Incorporate feedback and comments from design reviews, site inspections, and consultants into updated drawings.</li>
<li>Participate in technical coordination meetings to resolve drawing and interface issues.</li>
<li>Maintain organized drawing records and ensure all revisions are tracked, updated, and issued through document control procedures.</li>
<li>Follow company standards for title blocks, drawing numbering, layering, and line weights to maintain consistency.</li>
<li>Ensure all drawings comply with relevant codes and standards (e.g., IEC, NEC, SEC, SASO, or project-specific standards).</li>
<li>Implement QA/QC checks before submission to ensure completeness, accuracy, and consistency.</li>
<li>Adhere to company and industry standards and regulations in all drafted materials.</li>
<li>Provide accurate quantities and material take-offs from drawings to assist procurement teams.</li>
<li>Coordinate with site engineers to update as-built markups and reflect actual field conditions.</li>
<li>Assist in preparing shop drawing submittal packages, including specifications, datasheets, and layouts.</li>
<li>Follow HSSE procedures in office and site environments.</li>
<li>Maintain confidentiality of project data, design information, and client documents.</li>
</ul><p><b>
Requirements</b></p><ul>
<li>
Associate's degree or diploma in Autodesk AutoCAD.</li>
<li>7 - 12 years of relevant experience as an electrical draftsman in the construction or engineering industry.</li>
<li>Proficient in AutoCAD (2D/3D) and familiar with Revit MEP, BIM 360, or Navisworks for coordination.</li>
<li>Strong understanding of electrical principles, codes, and standards, including NEC.</li>
<li>Ability to interpret engineering specifications and technical drawings accurately.</li>
<li>Excellent attention to detail with a focus on producing high-quality and precise drawings.</li>
<li>Good communication and interpersonal skills for effective collaboration with team members.</li>
<li>Strong organizational skills with the capability to manage multiple projects and deadlines.</li>
<li>Ability to work independently as well as in a team environment.</li>
<li>Basic understanding of electrical systems, circuits, and load distribution to support design intent.</li></ul></div>

Electrical Draftsman

Explore 9+ Qc chemist in Jeddah Saudi Arabia this November. Find roles across top companies and apply now to boost your career.

9 qc chemist jobs IN Jeddah Saudi Arabia

QC Chemist

QC Chemist

QA/QC Architect

Histotechnologist / Histopathology Specialist

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

Production Planner

Electrical Draftsman