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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>


House of Measurement

<div>
 <p>
  <strong>
   About the Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are seeking a
  <strong>
   Chemist
  </strong>
  to support chemical analysis and research within our laboratory. In this role, you will conduct a variety of experiments, prepare samples, and perform analytical tests. This position is ideal for someone with a solid foundation in chemistry and hands-on laboratory experience, particularly in the fields of food or cosmetic chemistry.
 </p>
 <p>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in chemistry, Analytical Chemistry, or a related field.
  </li>
  <li>
   Minimum of 1 year of laboratory experience.
  </li>
  <li>
   knowledge of food, cosmetic, or analytical chemistry settings is highly preferred.
  </li>
  <li>
   Strong attention to detail, organizational skills, and the ability to follow protocols precisely.
  </li>
 </ul>
 <p>
 </p>
</div>


Chemist

Advanced Metals Company (AMCO)

<div>
 <p>
  <strong>
   Role Purpose
  </strong>
 </p>
 <p>
 </p>
 <p>
  To perform all planned QC/Inspection activities for workshop jobs and prepare necessary QC reports.
 </p>
 <p>
  To perform in-house calibration of measuring / testing instruments at planned intervals
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Accountabilities &amp; Activities
  </strong>
 </p>
 <p>
 </p>
 <ul>
  <li>
   Coordinate with workshop Foremen and carry out necessary inspection /QC checks of workshop job orders and prepare necessary stage inspection reports
  </li>
  <li>
   Witness pressure tests carried out by the production supervisors for the workshop jobs.
  </li>
  <li>
   Be responsible for the final inspection and release of workshop job orders after ensuring all QC activities are completed as per the Documentation &amp; Final Inspection check sheet.
  </li>
  <li>
   Perform in-house calibration of linear measuring instruments and calibration of in-house pressure gauges.
  </li>
  <li>
   Be responsible to keep the calibration status current and maintain the physical calibration status control tags on the instruments
  </li>
  <li>
   Notify QC Manager the calibration status of measuring or testing instruments to be calibrated externally and keep current as per planned frequencies.
  </li>
  <li>
   Raise Non-Conformance Reports (NCR) for the discrepant items at each stage of inspection and follow up with QC Manager for their close out.
  </li>
  <li>
   Perform all necessary activities to achieve Quality objectives set for the QA/QC Dept.
  </li>
  <li>
   Preparation of QC reports for completed job orders.
  </li>
  <li>
   Current Calibration status maintained for in-house measuring/testing instruments.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Education &amp; Certifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Mechanical Engineer/Diploma
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Years of Experience
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  4- 5 years experience
 </p>
</div>


Quality Control Inspector

Penspen

<div></div><div><p>Penspen is a leading energy services company, providing engineering, project management, asset management and integrity services to the energy industry worldwide for over 65+ years. Originally founded in the UK in 1954 as Spencer &amp; Partners, the company has now grown to include almost 1,000 members of staff, with major offices in London, Mexico, Colombia Houston and Abu Dhabi. (https://www.penspen.com)</p><br>
<p></p>
<p>
We are in search of a dedicated and experienced QA/QC Coordinator to join our team in Saudi Arabia.</p>
<p>
The QA/QC Coordinator will be responsible for overseeing quality assurance and quality control activities, ensuring compliance with project specifications and industry standards in the oil and gas sector.</p><br>
<p></p>
<p>
The primary location is outside KSA (TBC), you may be required to work in Al Khafji, KSA.</p>
<p>
QULIFICATIONS:</p>
<ul>
<li><p>Proven experience in coordinating QA/QC activities in the oil and gas or petrochemical industry, with a strong focus on project quality control/quality assurance.</p>
</li>
<li><p>In-depth knowledge of QA/QC principles, methodologies, and best practices.</p>
</li>
<li><p>Familiarity with relevant industry standards and regulations, such as ISO 9001, API, and ASME codes.</p>
</li>
<li><p>Excellent communication and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams and external stakeholders.</p>
</li>
<li><p>Strong analytical and problem-solving abilities, with a keen attention to detail.</p>
</li>
<li><p>Proficiency in QA/QC tools, software, and documentation management systems.</p></li></ul><br>
<p>
</p><p><b>Requirements:</b> <b>Education:</b></p>
<ul>
<ul><ul><li>Alternative (I): Bachelor&rsquo;s Degree in Engineering.</li>
<li>Alternative (II): Diploma or equivalent with a certificate from a recognized agency in QA/QC.</li>
</ul>
</ul></ul><p><b>Years of Experience:</b></p>
<ul>
<ul><li><p>Alternative (I): Ten (10) years of experience in coordinating QA/QC engineering and construction activities, with at least five (5) years in performing project quality control/quality assurance activities for Oil and Gas/Petrochemical projects.</p>
</li>
<li><p>Alternative (II): Fourteen (14) years of experience in coordinating QA/QC engineering and construction activities, with at least seven (7) years in performing project quality control/quality assurance activities for Oil and Gas/Petrochemical projects.</p>
</li>
</ul></ul><p>If you have the skills and are interested to apply, please share the CV by clicking this: https://careers.penspen.com/vacancy/qaqc-coordinator-597877.html#hs_show_apply_popup=true</p><br>
<p></p>
<p>
 #LI-BA1</p></div><p></p>

QA/QC Coordinator

Rashed Al Rashed & Sons Group

<div><div><div><div><div><div><h4 class="jobSectionHeader"><b>Job Description</b></h4>
<p></p><div><p><b>Location:</b> In-Kingdom</p>
<p><b>
Department:</b> QA/QC
</p><p><b>Reports To:</b> QA/QC Manager / Project Manager</p>
<p><b>
Job Summary:</b> Monitors and inspects welding activities to ensure compliance with project specifications, codes, standards, and quality requirements.</p>
<p><b>
Key Responsibilities:</b> - Has complete delegated authority to inspect all assurance/quality control matters at his assigned project. &ndash; Review welding procedures and material certifications. - Conduct visual inspections and NDT. - Identify welding defects and recommend corrective actions. - Maintain inspection reports and documentation. - Coordinate with engineers and QA/QC teams. - Ensure compliance with HSE regulations. - Support audits and certification processes.</p>
<p><b>
Qualifications &amp; Skills:</b> - Diploma or Bachelor&rsquo;s in Mechanical/Metallurgy/Engineering. - [5] years of experience as a Welding Inspector. - Knowledge of welding techniques, codes, and NDT methods. - Attention to detail and analytical skills. - Proficient in inspection reports. - Good communication and coordination skills.</p>
<p><b>
Preferred:</b> - CSWIP 3.1/2 or AWS-CWI (Certified Welding Inspector) preferred. NDT Certifications (RT, UT, PT, MT &amp; VT) - Experience with EPC, refinery, or oil &amp; gas projects. - Familiarity with regional codes in the GCC.</p>
<p><b>
Other Requirements: </b>-<b> </b>if (Engineer or Technician) in visa profession<b> </b>must<b> </b>register with Saudi Council of Engineers (SCE).</p></div><p></p>
<h4 class="jobSectionHeader"><b>Skills</b></h4>
<p></p><div><p><b>Qualifications &amp; Skills:</b> - Diploma or Bachelor&rsquo;s in Mechanical/Metallurgy/Engineering. - [5] years of experience as a Welding Inspector. - Knowledge of welding techniques, codes, and NDT methods. - Attention to detail and analytical skills. - Proficient in inspection reports. - Good communication and coordination skills.</p></div><p></p>
</div><p></p><div><div><h4 class="jobSectionHeader"><b>Job Details</b></h4>
<div><div>Job Location</div>
<div>Eastern Province, Saudi Arabia</div>
</div><div><div>Business Sector</div>
<div>Technical Maintenance &amp; Support</div>
</div><div><div>Company Type</div>
<div>Employer (Private Sector)</div>
</div><div><div>Functional Area</div>
<div>Maintenance, Repair &amp; Technical Services</div>
</div></div><div><h4 class="jobSectionHeader"><b>Preferred Candidate</b></h4>
<div><div>Career Level</div>
<div>Management / Supervisor</div>
</div></div></div></div><div><h4 class="jobSectionHeader"><b>About This Company</b></h4>
<p></p><div><div><h3 class="jobSectionHeader"><b>AlRashed Group</b></h3>
 <div></div><div><div><div>Khobar, Saudi Arabia</div>
 </div><div></div><div><div>500 employees or more</div>
 </div><div></div><div><div>+123.1.234.567</div>
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QC Inspector - Welding

Ladun 

<p><b>We are hiring: QA/QC Engineer </b></p><p><b>Key Responsibilities:</b></p><ul><li>Develop and implement QA/QC procedures for aluminum and steel works.</li><li>Conduct inspections, audits, and tests to ensure compliance with standards.</li><li>Review material certificates, method statements, and ITPs.</li><li>Report non-conformities and follow up on corrective actions.</li></ul><p><b>Qualifications:</b></p><ul><li>Bachelor&rsquo;s degree in mechanical, Civil, or Industrial Engineering.</li><li>3&ndash;5 years of QA/QC experience in the manufacturing or fabrication industry.</li><li>Strong understanding of quality standards and procedures.</li></ul><p><b>To Apply:</b><br/>Send your CV to [career@ladun.sa] with the job title in the subject line.</p><p>Job Type: Full-time</p>

QA/QC Engineer

Explore 82+ Qc chemist in Saudi Arabia this November. Find roles across top companies and apply now to boost your career.

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QC Inspector - Welding

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