supervisor quality control

Fulkrum

<div>Join Fulkrum &ndash; Be Part of a Global Success Story 
Fulkrum is a global leader in inspection, expediting, auditing, and technical staffing services, delivering exceptional solutions to the energy, engineering, and construction industries for over 14 years. Headquartered in the UK, we have established a strong presence across six continents, serving more than 300 clients worldwide. 

Our commitment to excellence has been recognised with prestigious awards, including the King's Award for Enterprise in International Trade (2023), the People and Competency Award at the EIC Awards (2023), and the Scale-Up Award at the WESCA North America Awards (2024). Most recently, Fulkrum was named the 2025 winner in the People, Culture &amp; Optimisation category at the EIC North &amp; Central America Regional Awards. 
One of our esteemed clients in India is currently seeking a Mechanical - Procurement Quality Control Supervisor (PQCS) to join their team in Vadodara, India. This role begins with an initial assignment in India and may transition to Saudi Arabia based on project requirements. 
Key Responsibilities:
<ul>
<li>Oversee procurement quality control for mechanical packages and equipment.</li>
<li>Ensure supplier compliance with quality standards, specifications, and project requirements.</li>
<li>Conduct inspections, audits, and reviews during procurement and fabrication stages.</li>
<li>Coordinate with vendors, engineering, and project teams to resolve quality issues.</li></ul> 


Location:
<ul>
<li>Vadodara, India &ndash; Initial assignment (approx. 1.5 years)</li>
<li>Saudi Arabia &ndash; Potential relocation after initial period</li></ul> 


Role Requirements:
<ul>
<li>Degree or Diploma in Mechanical Engineering</li>
<li>Minimum of 10 years of relevant experience</li>
<li>At least 3 years of experience in an ARAMCO PQCS role</li>
<li>Strong experience in procurement quality control and vendor inspections.</li>
<li>Knowledge of international codes/standards (ASME, ASTM, ISO, etc.).</li>
<li>Excellent communication and coordination skills</li></ul> 


This is a great opportunity for professionals looking to work on international projects and grow within a dynamic environment.</div>

Procurement Quality Control Supervisor (PQCS)

Philip Morris International

<div>Supervisor Manufacturing Quality 
Be a part of a revolutionary change. 
At PMI, we&rsquo;ve chosen to do something incredible. We&rsquo;re totally transforming our business, and building our future on smoke-free products. 
With huge change, comes huge opportunity. So, wherever you join us, you&rsquo;ll enjoy the freedom to dream up and deliver better, brighter solutions and the space to move your career forward in endlessly different directions. 
It&rsquo;s so rare in R&amp;D that everything aligns to create the ideal conditions for outstanding work. Right now, at PMI, that&rsquo;s exactly what&rsquo;s happening. R&amp;D is the driving force for our bold new vision: to replace cigarettes with a revolutionary portfolio of alternative products. 
Join us and you&rsquo;ll have the resources, support and technology you need to break new ground and see ideas come to life. You&rsquo;ll be surrounded by some of the brightest scientists in their fields, with fast access to subject experts and commercial decision-makers. 
If you&rsquo;re creative, courageous and ready to take risks, you can make a huge impact and propel your career in an endless number of directions. Ultimately, by delivering our smoke-free and beyond nicotine future 
Your &lsquo;day to day&rsquo; 
As a Supervisor Manufacturing Quality, you will plan, organize and control all Manufacturing Quality activities for both Conventional and RRP products. You will also, supervise and develop the manufacturing quality team in order to continuously support Production while providing Quality on the floor support to ensure an optimal and cost effective quality assurance and contribute to the achievement of quality and volumes objectives, up to the release of finished goods. In addition, you will ensure that all activities are performed in Compliance with the Quality System and regulations. You will also consistently apply OPEN+ standards, supporting the elimination of quality losses. 
More specifically, you'l 
<ul><li>
Ensure compliance to all PMI and legal standards, policies and standards related to Environment, Health, Safety, Sustainability to prevent personnel, asset or societal loss. Act and promote an interdependent and transparent safety culture fostering the utilization of preventive/predictive approach in line with Open+/IOS.</li><li>
Guarantee the required on floor Quality Support for RRP and Conventional products in order to meet and sustain the PMI quality standards, assure self-inspection process through effective and efficient sampling plan, statistical process control (SPC), and/or digital quality control (Zoom QC). Ensure that quality practices/requirements are shared and deployed on the floor by transferring knowledge and training to Quality Champions on new processes, requirements, methodologies or procedures.</li><li>
Provide full support in case of non-conformities, both for product and process. Provide guidance and coordinate Quality team members when needed during investigations, risk assessment and root causes analysis, using OPEN+ problem solving tools. Ensure that non-conformities are investigated in a timely manner and products/materials blocked when required. Ensure that product non-conformity and related NC-CAPA processes are led in order to ensure that quality improvement opportunities are identified, prioritized and action plans implemented. Approve/reject all non-conformities and action the plan raised.</li><li>
Participate in the creation and review of procedures, work instructions and other Quality Documents that are required. Provide the related support and training in accordance with the training management system.</li><li>
Provide first level support to Manufacturing related to material issues (Troubleshooting) until mitigation and communicate/raise to related parties accordingly.</li><li>
Provide timely feedback and recommendations for corrective actions to ensure performance objectives achievement, support continuous improvement and procedures implementation.</li><li>
Propose, define and implement quality improvement programs to ensure products and processes meet Quality requirements along manufacturing lines using OPEN+ tools, in order to achieve a leading position on quality and to propose cost savings.</li><li>
Perform regular control on the QA LOGD cost regarding semis, FG and DIMs by timely screening blocked stock, taking prompt decision and booking the cost accordingly.</li><li>
Lead and develop a motivated and skilled team to ensure performance levels, professional development and achievement of objectives, in respect of PMI leadership model.</li><li>
 Create an environment in which each member of the team is motivated to express own talent and potential.</li><li>
Develop and drive the execution of a Qualification matrix and training path for each role.</li><li>
Act as Pillar Member and contribute to the full year pillar plan definition and implementation aligned with OPEN+ Phase journey.</li><li>
Participate and contribute to pillar reviews definition and implementation as per defined frequency. Be responsible for implementation of Standard work process defined in Pillars.</li><li>
Ensure self and team capabilities based on step-up cards.</li></ul> 
Who we&rsquo;re looking fo 
<ul><li>
College/University (Master's degree) in Biological Sciences, Physical Sciences, Chemistry, Engineering or relevant skills through demonstrated experience</li><li>
Minimum 5 years' experience in quality assurance in tobacco, food, pharmaceutical, FMCG or similar industry preferably in a managerial role.</li><li>
Knowledge of manufacturing process and applicable QMS, International standards (ISO).</li><li>
Demonstrated knowledge on Quality tools, root cause analysis and analytical skills.</li><li>
Sound IT skills (Office).</li><li>
Fluency in both written and spoken English/Turkish is a must.</li></ul> 
What we offer 
Our success depends on the people who come to work every single day with a sense of purpose and an appetite for progress. 
Join PMI and you too can: 
<ul><li>
Seize the freedom to define your future and ours. We&rsquo;ll empower you to take risks, experiment and explore.</li><li>
Be part of an inclusive, diverse culture, where everyone&rsquo;s contribution is respected; collaborate with some of the world&rsquo;s best people and feel like you belong.</li><li>
Pursue your ambitions and develop your skills with a global business &ndash; our staggering size and scale provides endless opportunities to progress.</li><li>
Take pride in delivering our promise to society: a smoke-free future.</li></ul></div>

Supervisor Manufacturing Quality

Rise Technical Recruitment

Civil QC Supervisor Talacre (North Wales) Onshore site - 24 months + Contract - Project expected to last 2/3 years 575 - 630 a day Outside IR35 - Onsite work 5.5 days per week Are you looking for a long term contract Outside IR35 role with an excellent day rate working on EPC projects within the Oil and Gas industry? This role will be working on a Carbon Capture project offshore in Liverpool bay with the project expected to last 2/3 years. The role will be Monday - Friday with some Saturday work 8-1pm. This role is perfect for someone with QC supervisory experience working within the Oil and gas or similar industry. In this role you will supervise a team of QC inspectors, whilst ensuring Quality Control Plans are correctly carried on out liaise with the end client. The company are a market leader in the EPC sector market specilaising in onshore and offshore projects. The Role:<ul><li>Supervise and witness inspections, ensuring approved Quality Control Plans and documentation are correctly implemented and recorded, including subcontracted activities.</li></ul> <ul><li>Verify preparation and completeness of Quality dossiers for final handover and ensure proper management of materials, equipment, and calibration records.</li></ul> <ul><li>Support and monitor qualification of inspection personnel, QC system rules, and work procedures, including special processes.</li></ul> <ul><li>Ensure NCR management, inspections, and testing are effectively carried out per QC and ITP requirements, with all records properly collected for mechanical completion</li></ul>The Person:<ul><li>Proven experience as Civil QC in a management/Supervisory role.</li><li>Oil and gas experience or similar</li><li> ISO 9001:2015 certified</li><li> Degree in Civil Engineering or equivalent</li></ul> For Further information please contact William Technical. Refrence - BBBH(phone number removed)<img src="https://www.jobg8.com/Tracking.aspx?jJgsV495VLehxi9wM9UWJ2vC99EAREZMw" width="0" height="0" />

Civil Quality Control Supervisor

<div>Company Description 
We are SGS &ndash; the world&rsquo;s leading testing, inspection and certification company. We are recognized as the global benchmark for quality and integrity. Our 93,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. 
Job Description<ul><li> 
Key Responsibilities:</li><li>
Supervise all quality control activities and inspections related to mechanical, piping, structural, electrical, and instrumentation works on the offshore site.</li><li>
Ensure compliance with Aramco standards (SAEPs, SAICs, SAMSSs) and project-specific QA/QC plans.</li><li>
Review and approve inspection test plans (ITPs), method statements, and material inspection reports.</li><li>
Conduct joint inspections with the client (Aramco) and prepare necessary documentation for approval.</li><li>
Monitor the implementation of approved welding procedures, NDT, coating, and material traceability programs.</li><li>
Coordinate with the construction team to ensure timely inspection and release of work.</li><li>
Ensure proper calibration and maintenance of inspection equipment.</li><li>
Manage and mentor QC inspectors across various disciplines.</li><li>
Prepare and submit daily/weekly QC progress reports and non-conformance reports (NCRs).</li><li>
Lead root cause analysis and corrective/preventive action implementation for quality issues.</li><li>
Support QA Manager in internal and external audits.</li><li>
Ensure that all offshore quality control documentation is properly recorded and traceable.</li></ul> 
Qualifications<ul><li> 
Bachelor&rsquo;s Degree or Diploma in Engineering (Mechanical).</li><li>
Aramco Approval as QC Supervisor or Engineer (valid and verifiable).</li><li>
Minimum 8&ndash;10 years of QA/QC experience in the oil &amp; gas EPC industry, with at least 5 years in offshore projects.</li><li>
Strong knowledge of ASME, AWS, API, ISO, and ASTM standards.</li><li>
Experience with offshore structures, piping, mechanical equipment installation, and coatings inspection.</li><li>
Familiarity with Aramco documentation systems (QMIS / SAIC / ITP formats).</li><li>
Valid Offshore Safety &amp; Survival (BOSIET / HUET) and Medical Fitness Certificates.</li><li>
Proficient in MS Office and quality management systems.</li><li>
Excellent leadership, communication, and reporting skills.</li></ul>
Preferred Certifications:<ul><li>
CSWIP 3.1 / AWS-CWI (for welding inspection)</li><li>
ISO 9001:2015 Internal Auditor Certification</li></ul>
Key Competencies:<ul><li>
Strong understanding of offshore safety and quality culture</li><li>
Effective team leadership and coordination with multidisciplinary teams</li><li>
Analytical mindset and problem-solving abilities</li><li>
Excellent communication and documentation skills</li></ul> 
Additional Information 
Please attach your CV, Technical Certificates, Approval Documents and relevant documents</div>

Quality Control Supervisors ( QCS ) - Mechanical ( Welding )

Bosta

<div>
 Launched in 2017, Bosta is an overnight delivery provider for E-commerce companies in Egypt and KSA. Leveraging technology to empower businesses is what we do best. Our goal is to disrupt the logistics industry by bringing technology and experience all together to provide a one-stop shop for delivery solutions.
 
 
 We rely on advanced technology to deliver orders to our customers in a fast way. Businesses can track and connect with couriers and follow up on their orders - all in one system.
 
 
 Role Overview
 
 
 The Quality Supervisor will be responsible for overseeing key performance indicators (KPIs) across the operations cycle, ensuring process compliance, and driving continuous improvement. This role requires a detail-oriented professional with strong analytical and stakeholder management skills, capable of identifying root causes of issues and implementing corrective action plans.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Own and manage specific KPIs end-to-end, ensuring performance meets targets
 </li>
 <li>
 Monitor daily/weekly performance trends, highlight risks, and drive improvement actions
 </li>
 <li>
 Conduct root cause analysis on recurring issues and define corrective and preventive actions
 </li>
 <li>
 Prepare and present performance reports to management and stakeholders
 </li>
 <li>
 Collaborate closely with cross-functional teams to address quality gaps and ensure smooth workflows
 </li>
 <li>
 Support training initiatives to improve compliance and awareness among operational teams
 
 
 
 </li>
 </ul>
 
 Qualifications &amp; Skills
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Business Administration, Operations, Supply Chain, or related field
 </li>
 <li>
 3&ndash;5 years of experience in Quality Assurance/Control, preferably in logistics, shipping, or operations
 </li>
 <li>
 Strong analytical skills with experience in data-driven decision making
 </li>
 <li>
 Excellent problem-solving skills with the ability to identify and resolve issues effectively
 </li>
 <li>
 Strong stakeholder management and communication skills
 </li>
 <li>
 Proficiency in MS Office (Excel, PowerPoint, Word); knowledge of data visualization tools is a plus
 </li>
 <li>
 Willingness to travel for hub visits and audits
 
 
 
 </li>
 </ul>
 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
</div>

Operations Quality Control Supervisor

E2 Optics

<div><div>Join our team and shape the future of connectivity: QA/QC Supervisor at E2 Optics!</div><div>
</div><div>
CLICK HERE to learn more!</div><div>
</div><div>
Are you ready to take your career to the next level? At E2 Optics, we&rsquo;re not just offering a job&mdash;we&rsquo;re offering an opportunity to be part of something extraordinary! 
</div><div></div> 
<div>The Quality Assurance/Quality Control (QA/QC) Supervisor is responsible for developing, maintaining, updating, deploying, training and successful implementation of the E2 Optics Quality Management System(QMS) to ensure that project quality is delivered in accordance with industry and customer standards. The QA/QC role includes planning, coordinating, collaborating and partnering with internal and external parties to support the successful execution within the framework of the E2 Optics QMS and foster continuous improvement activities. This includes supporting the sharing, anchoring and training of the quality system elements at other relevant sites across the program.</div><div>
</div><div>
Why E2 Optics?</div><div>
Award-winning, Women-Owned: One of America's largest and fastest growing low voltage solution provider.</div><div>
Innovative Culture: We thrive on creativity and bold ideas. Here, your voice matters, and your contributions drive our success.</div><div>
Growth Opportunities: From professional development to career advancement, we&rsquo;re committed to helping you reach your goals.</div><div>
Dynamic Environment: Work in a vibrant, fast-paced setting where every day brings new challenges.</div>
<h3 class="jobSectionHeader">What You'll Do:</h3><ul><li>
Safety is our number one Core Value. Follow safe work practices and company and client work site policies.</li><li>
Promote E2Core Values to foster and safeguard a family-centric culture.</li><li>
Develop, update, implement and deploy the E2 Optics QMS in accordance to the program structure across the site and assist other program sites to implement as requested.</li></ul><ul><li>
Train and coach QA/QC Coordinators and internal employees to integrate quality initiatives into the daily workstream.</li><li>
Collaborate with the program representatives to coordinate and integrate applicable quality specifications and expectations in to both the E2 QMS and client&rsquo;s quality program.</li><li>
Technical writing -Ability to develop QA/QC installation and technical reference, procedure, inspection, and report documents as required to support E2 Optics QMS and client&rsquo;s quality program.</li><li>
Ability to develop and implement QA/QC structure and tools to promote a quality awareness culture. Partner with field staff for successful implementation and execution.</li></ul><ul><li>
Ensure Quality Assurance standards are developed and disseminated to relevant stakeholders.</li><li>
Must be able to operate equipment such as scissor lifts, telehandlers, boom lifts, and UTVs (buggies) if required to do so.</li><li>
Travel: The individual in this role should be able and willing to travel as required by E2.</li></ul><h3 class="jobSectionHeader">
What We're Looking For:</h3><ul><li>
Education: Associate&rsquo;s Degree in Construction Management, Project Coordination or similar; experience may substitute.</li><li>
Experience: 2 to 4 year&rsquo;s field experience new build installations and testing fiber.</li><li>
Data Center structure cabling experience.</li><li>
Certifications: BICSI certifications (TE350 Technician, RTPM).</li><li>
Skills: Working knowledge of Quality Management Systems and relevant software platforms.</li><li>
Strong leadership, communication, coaching and collaborative skills.</li><li>
Exceptional analytical, decision making and problem-solving skills.</li><li>
Ability to add value both independently and as a team member.</li><li>
Demonstrate professionalism with ability to engage effectively to build rapport across all employee levels; management, staff, customers, vendors, contractors and others</li></ul><div>
WHAT WE OFFER:</div><ul><li>Competitive pay</li><li>Opportunities for professional development and career growth.</li><li>BICSI Training Facilities</li><li>A supportive and inclusive work environment.</li><li>Health, dental, and vision insurance.</li><li>Paid time off and holidays.</li></ul><div></div><div> 
WORK ENVIRONMENT &amp; PHYSICAL DEMANDS: The standard work environment for this position is an indoors business office and construction environment. Ability to use a computer and/or hand tools while sitting or standing for extended periods of time. The noise level in the work environment is usually moderate. While performing the duties of this job, the employee is regularly required to sit, talk or hear, use hands, stoop, kneel, bend, rotate, push, pull, reach with hands and arms on intermittent to regular basis daily. The employee is frequently required to stand and walk. The employee must regularly lift and/or move up to 50 pounds and frequently lift and/or move up to 25 pounds. The employee must regularly carry and climb ladders to 20 feet. The employee may be required to work in tight, confided spaces. The employee must demonstrate regular and on-time attendance. There could be a requirement of occasional travel by conventional means including aircraft, motor vehicle and the like within the region and to other locations as required. The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job.</div><div></div><div> 
DISCLAIMER: The above job definition information has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Job duties and responsibilities are subject to change based on changing business needs and conditions.</div><div>
An Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Actively recruits qualified women, minorities, disabled and veterans for all positions for which they are qualified.</div><div></div><div> 
TEXTING TERMS OF SERVICE: We may send text messages you have consented to receive. Message frequency may vary. You can cancel text messages at any time by texting &quot;STOP&quot;. After you send &quot;STOP&quot;, we may send you an additional text message to confirm that you have been unsubscribed. You will no longer receive text messages from that phone number, or from any member of our team. If at any time you have questions about the text messages, text &quot;HELP&quot;. After you send &quot;HELP&quot; we will respond with instructions on how to use our service as well as how to unsubscribe. Message and data rates may apply.</div>

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.</div>

QA/QC Supervisor

Amerikan Hastanesi

<div>
 
 Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of cellular products such as; Car-T/TILs, Mesenchymal Stem Cells (MSCs), exosomes, immunotherapy products, cord blood banking and tissue grafts. We are committed to delivering high-quality, regulatory-compliant cell therapy products through rigorous quality control and validation processes.
 
 
 
 
 
 We are seeking an experienced and strategic
 
 Head of Quality Control for Stembio
 
 to lead and oversee all quality control (QC) activities for our cell therapy products.
 
 
 
 
 
 This role is responsible for ensuring the accuracy, reliability, and compliance of QC testing, maintaining product integrity, and upholding regulatory and cGMP standards. The ideal candidate will have extensive experience in analytical testing, method validation, and laboratory operations, along with a proactive approach to continuous improvement and compliance.
 
 
 
 
 
 If you are passionate about quality control in advanced cell therapies and have the expertise to uphold the highest standards, we encourage you to apply!
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 Advanced degree (PhD, or equivalent) in Biology, Biochemistry, Analytical Chemistry, or a related field.
 </li>
 <li>
 Minimum of 5 years of experience in Quality Control within preferably a GMP-regulated biopharmaceutical or cell therapy environment or Academia.
 </li>
 <li>
 Strong expertise in analytical techniques such as flow cytometry, PCR, ELISA, HPLC, and microbiological testing.
 </li>
 <li>
 Proven leadership experience, with the ability to manage and develop high-performing teams.
 </li>
 <li>
 Deep understanding of regulatory requirements (cGMP, TITCK, EMA, ICH) and industry best practices for QC.
 </li>
 <li>
 Excellent problem-solving skills, attention to detail, and a commitment to continuous improvement.
 </li>
 </ul>
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 <ul>
 <li>
 Lead and manage the Quality Control department, ensuring all testing activities meet regulatory, company, and cGMP standards.
 </li>
 <li>
 Oversee analytical, microbiological, and raw material testing to ensure product safety, efficacy, and consistency.
 </li>
 <li>
 Drive method validation, transfer, and optimization to support robust and reliable analytical processes.
 </li>
 <li>
 Collaborate with manufacturing, quality assurance, and regulatory teams to maintain product quality throughout the lifecycle.
 </li>
 <li>
 Ensure compliance with CGMP, TITCK, EMA, and other regulatory requirements through rigorous documentation, data integrity, and audit readiness.
 </li>
 <li>
 Manage laboratory operations, including equipment qualification, personnel training, and process improvements.
 </li>
 <li>
 Implement and oversee stability studies, environmental monitoring, and trending analysis to detect and prevent potential quality issues.
 </li>
 <li>
 Lead investigations and corrective actions for out-of-specification (OOS) results, deviations, and other QC-related issues.
 </li>
 <li>
 Stay current with industry advancements and regulatory changes to ensure the QC function remains best-in-class.
 </li>
 </ul>
 
 
 
 
 
 Your personal data is processed for the purpose of receiving and evaluating your job application. You can find detailed information about your processed personal data and rights from the "Employee Candidate Clarification Text" under the "Human Resources" heading of our website.
 
 
 
 
</div>

Stembio - Head of Quality Control

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