quality control expert

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 a highly skilled and motivated
 
 Quality Assurance (QA) Expert for Stembio
 
 to ensure compliance with cGMP, regulatory requirements, and company quality standards for our cell therapy products.
 
 
 
 
 
 The QA Expert will oversee quality management systems, support regulatory audits, manage deviations, and drive continuous improvement initiatives. The ideal candidate will have a strong background in quality assurance, risk management, and compliance within a cGMP-regulated environment.
 
 
 
 
 
 If you are passionate about quality assurance in advanced cell therapies and have the expertise to uphold the highest standards, we encourage you to apply!
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 Master&rsquo;s degree or higher in Biology, Biotechnology, Biochemistry, or a related field.
 </li>
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 Minimum of 3+ years of experience in a cGMP-regulated Quality Assurance environment, preferably in cell therapy, regenerative medicine, or biopharmaceuticals.
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 Strong knowledge of quality assurance principles, risk management, and regulatory compliance (EMA, TITCK, FDA, ICH guidelines).
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 Experience in managing QMS, deviation handling, CAPA, and change control processes.
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 Ability to interpret and apply regulatory guidelines and quality standards to ensure compliance.
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 Excellent analytical, problem-solving, and decision-making skills.
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 Strong communication and leadership skills, with the ability to work independently and in a team.
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 Experience with electronic QMS, document control systems, and LIMS is a plus.
 </li>
 </ul>
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 <ul>
 <li>
 Ensure compliance with cGMP, EMA, TITCK, and other relevant regulatory requirements for cell therapy products.
 </li>
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 Develop, implement, and maintain Quality Management Systems (QMS), including deviation management, CAPA, change control, and risk assessments.
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 Support and participate in regulatory inspections, audits, and internal quality reviews.
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 Review and approve SOPs, batch records, validation protocols, and quality-related documents.
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 Conduct investigations for deviations, out-of-specification (OOS) results, and non-conformances, ensuring timely resolution and implementation of corrective and preventive actions (CAPAs).
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 Oversee the training program to ensure all personnel are adequately trained in quality procedures and regulatory requirements.
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 Collaborate with cross-functional teams including Quality Control (QC), Production, and Regulatory Affairs to maintain high-quality standards.
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 Monitor and improve quality metrics to ensure continuous improvement of quality systems and processes.
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 Manage supplier and raw material quality assurance, including vendor qualification and material release processes.
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 Ensure timely approval and release of raw materials, intermediates, and final products based on quality assurance criteria.
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 </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 - Quality Assurance (QA) Expert

INNOVENT INTEGRATED SOLUTION FZ LLC

<div> Job Summary <div> The Quality Control (QC) Specialist will ensure that our products and services meet the highest quality standards through rigorous testing and evaluation. This role involves developing and implementing quality control procedures, conducting inspections, and collaborating with teams to resolve quality issues. The ideal candidate will have a keen eye for detail, strong analytical skills, and experience with quality control methodologies. They will be responsible for maintaining detailed records of quality control activities, conducting root cause analysis, and implementing corrective actions. This role is vital in ensuring customer satisfaction and maintaining our reputation for high-quality products. </div> </div> <div> What you'll do <div> <ul> <li>Develop and implement quality control procedures and standards.</li> <li>Conduct inspections and tests on products and services.</li> <li>Identify, document, and track defects and inconsistencies.</li> <li>Collaborate with development and production teams to resolve quality issues.</li> <li>Maintain detailed records of quality control activities.</li> <li>Conduct root cause analysis and implement corrective actions.</li> <li>Ensure compliance with industry standards and regulations.</li> <li>Train staff on quality control processes and best practices.</li> <li>Continuously improve quality control processes and procedures.</li> </ul> </div> </div> <div> Qualifications <div> <ul> <li>Bachelor s degree in Quality Management, Engineering, or related field.</li> <li>5+ years of experience in quality control or quality assurance.</li> <li>Strong knowledge of quality control methodologies and tools (e.g., Six Sigma, ISO standards).</li> <li>Excellent attention to detail and analytical skills.</li> <li>Strong communication and documentation skills.</li> <li>Ability to work collaboratively with cross-functional teams.</li> <li>Experience with quality control software and tools.</li> <li>Relevant certifications (e.g., Certified Quality Engineer) are a plus.</li> </ul> </div> </div> <div> <div> <div>Let's explore how Innovent can work with you!</div> <div>Please fill in the form with your details to book a meeting with our team.</div> </div> <div></div></div>

Quality Control (QC) Specialist

Healthy Calorie

Job Title: Chef (Quality Controller &ndash; QC)Department: Kitchen / Quality ControlReports To: Head Chef / Quality Manager / Kitchen SupervisorJob Purpose:The Chef (Quality Controller) is responsible for ensuring that all food prepared and served meets the established quality, hygiene, and presentation standards. This role involves monitoring food production processes, conducting regular checks, and collaborating with kitchen staff to maintain consistency and compliance with food safety regulations.Key Responsibilities:<ul><li>Monitor all stages of food preparation to ensure quality standards are met.</li><li>Conduct visual, taste, and temperature checks on dishes before they are served.</li><li>Ensure adherence to hygiene, sanitation, and food safety protocols (e.g., HACCP).</li><li>Inspect raw materials for freshness and quality before use.</li><li>Coordinate with chefs and kitchen staff to improve food presentation and portioning.</li><li>Identify and report any deviations from quality standards or recipes.</li><li>Maintain records of quality checks, temperatures, and compliance reports.</li><li>Assist in training kitchen staff on quality control procedures.</li><li>Ensure proper storage, labeling, and rotation of food items (FIFO system).</li><li>Collaborate with procurement to ensure ingredients meet quality requirements.</li></ul>Qualifications and Skills:<ul><li>Diploma or certification in Culinary Arts, Food Technology, or related field.</li><li>Minimum 2-3 years of experience in a culinary or food quality control role.</li><li>Strong knowledge of food safety standards (e.g., HACCP, ISO 22000).</li><li>Excellent attention to detail and sensory evaluation skills.</li><li>Good communication and teamwork abilities.</li><li>Ability to work in a fast-paced environment and handle multiple tasks.</li></ul>Working Conditions:<ul><li>Standing for long periods in a kitchen environment.</li><li>Exposure to heat, steam, and kitchen equipment.</li><li>May involve weekend and evening shifts, depending on operational needs</li></ul>Job Type: Full-timePay: BD180.000 - BD220.000 per month

Chef (QC ) Quality controller

Baker Hughes

Overview Quality Records Control SpecialistWould you like to be part of a team that puts quality first?Are you passionate about delivering quality through meeting standards and procedures?Join Baker Hughes.We are the leader in well construction and production. Our innovative physical and digital solutions improve efficiency, production and maximize reservoir value. Our team ensures high quality, consistency and reliability for all products throughout the complete life-cycle of our manufacturing production process. Partner with the best As a Quality Records Control Specialist, you'll be the focal point for all QA/QC assessment for Oilfield business. Conducting qualitative risk assessments, root cause analysis and providing corrective actions. Supporting QMS system by creating, editing and reviewing documents to be aligned with Baker Hughes global standards.As a Quality Records Control Specialist, you will be responsible for:<ul><li>Conducting qualitative risk assessments and root cause analysis and corrective actions, aligned to continuous improvement.</li><li>Using quality tools to monitor and improve processes, supporting QMS system according to Baker Hughes standards.</li><li>Engaging with internal auditing teams and participating in audits</li><li>Participating in improvement initiatives</li><li>Participating in tender & contract reviews and the development of quality plans to support contracts</li><li>Conducting business activities in accordance with Baker Hughes HSE policies, Legal Compliance requirements and Company Core Values.</li></ul> Fuel your passion To be successful in this role you will need to:<ul><li>Have Industrial/ Technical Diploma or minimum 5 year of equivalent experience in quality ( oil and gas environment)</li><li>Have experience in Flow Assurance, Production Optimization product testing in oil and gas equipment</li><li>Preferably have experience in documentation.</li><li>Have good analytical skills with good written, verbal communication and presentation skills</li><li>Have team player attitude</li><li>Have good understanding of quality systems and industry standards.</li><li>Have good quality control, calibration and business process modelling skills</li></ul> Work in a way that works for you We recognize that everyone is different and that the way in which people want to work and deliver at their best is different for everyone too. In this role, we can offer the following flexible working patterns:<ul><li>Please discuss your working patterns with the recruiter during the process</li></ul> Working with us Our people are at the heart of what we do at Baker Hughes. We know we are better when all of our people are developed, engaged and able to bring their whole authentic selves to work. We invest in the health and well-being of our workforce, train and reward talent and develop leaders at all levels to bring out the best in each other. Working for you Our inventions have revolutionized energy for over a century. But to keep going forward tomorrow, we know we have to push the boundaries today. We prioritize rewarding those who embrace change with a package that reflects how much we value their input. Join us, and you can expect:<ul><li>Contemporary work-life balance policies and wellbeing activities</li><li>Comprehensive private medical care options</li><li>Safety net of life insurance and programs</li><li>Tailored financial programs</li><li>Additional elected or voluntary benefits</li></ul> About Us We are an energy technology company that provides solutions to energy and industrial customers worldwide. Built on a century of experience and conducting business in over 120 countries, our innovative technologies and services are taking energy forward - making it safer, cleaner and more efficient for people and the planet.Join Us:Are you seeking an opportunity to make a real difference in a company that values innovation and progress? Join us and become part of a team of people who will challenge and inspire you! Let's come together and take energy forward.Baker Hughes Company is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, national origin, age, disability, veteran status or other characteristics protected by law.<img src="https://www.jobg8.com/Tracking.aspx?m1MhrCgiSOgYVrZgrd2BHrkfG5YTx50rc" width="0" height="0" />

Quality Records Control Specialist

Amros Pharmaceuticals

Hirings.1- Senior QC Officer1-2 years of experience Male &amp; Female both can apply2- QC Executive 4-5 years of Experience Only Males RequiredNote:Must Have Pharmaceutical ExperienceQC ExecutiveWe are looking for a sharp, experienced QC Executive to join our Quality Control team.Core Responsibilities:Execute and oversee analytical testing of raw materials, in-process samples, and finished products.Ensure strict adherence to all regulatory guidelines.Review and approve QC records, analytical reports, and maintain laboratory documentation.Investigate OOS/OOT results and manage deviations/CAPA.Participate in analytical method validation, transfer, and equipment qualification.Qualifications:Bachelor's or Master's degree in Pharmacy or a related science field.4-5 years of mandatory QC experience in Pharma Manufacturing.Strong technical proficiency in major analytical techniques and regulatory compliance (cGMP).Excellent communication, documentation, and problem-solving skills.If you are detail-oriented and committed to pharmaceutical quality, apply today to help us ensure product safety and efficacy!Apply Here: hr.recruitment@amrospharma.comJob Type: Full-timeExperience:<ul><li>Pharmaceutical: 2 years (Required)</li></ul>Work Location: In person

Quality Control Executive

Minapharm Pharmaceuticals

<div>
 
 
 
 
 About Minapharm:
 
 
 
 
 
 Minapharm Pharmaceuticals is a leading pharmaceutical company in Egypt and the Middle East and the largest end-to-end manufacturer of biological therapies in MEA with over 20 years of experience in cellular and bioprocess engineering. Headquartered in Cairo, Minapharm commercializes over 100 life-saving and life-enhancing products ranging from small molecules to complex bioengineered proteins and viral vectors, with an impressive immunotherapy pipeline. Together with its wholly-owned Berlin-based subsidiary, ProBioGen AG - a world-leading CDMO, Minapharm has established an integrated business model making it the only gene-to-market company in the region. Consolidating its international platform of intelligent biopharmaceutical technologies with the longstanding process development and manufacturing expertise in the MEA, Minapharm, together with ProBioGen, has incorporated MiGenTra GmbH headquartered in Berlin and manufacturing in Cairo, to enhance the accessibility to critical healthcare transforming medicines through product development and commercialization of Biosimilar mABs, Cell, and Gene Therapies and vaccines, at affordable prices in Egypt, and MEA.
 
 
 
 
 
 
 
 
 Our Values:
 
 
 
 
 
 &middot; Diversity &amp; Respect
 
 
 &middot; Integrity &amp; Accountability
 
 
 &middot; Collaboration
 
 
 &middot; Leadership &amp; Empowerment
 
 
 &middot; Innovation &amp; Continuous Learning
 
 
 
 
 
 
 
 
 Job Summary:
 
 
 
 
 
 Coordinate, implement and report process validation inside production departments to verify the continuous capability of production processes to comply with local authorities, WHO, EU regulations and fulfill cGMP guidelines.
 
 
 
 
 
 
 
 
 Duties &amp; responsibilities:
 
 
 
 
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 Follow up the monthly plan and communicate with production departments to perform the required validation tasks.
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 Create formulas and recipes on ERP.
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 Prepare validation protocol
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 Witness the different processes of manufacturing, withdraw samples and send it to quality control department to analyze the samples.
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 Withdraw cleaning validation samples from production machines to ensure their compliance with cGMP.
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 Issue validation report with outcomes of the validation and statistical process analysis.
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 Share in qualification activities, thermal validation, mapping and CSV
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 Prepare relevant SOPs, procedures.
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 Batch record review to ensure compliance with cGMP.
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 Deviation reporting &amp; set CAPAs
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 Create &amp; Review qualification reports.
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 Carry out any additional job-related tasks that are assigned.
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 </ol>
 
 
 
 
 
 
 
 Qualifications:
 
 
 
 
 <ul>
 <li>
 6-9 years of relevant experience in pharmaceutical industry.
 </li>
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 B.SC of pharmacy or engineering
 </li>
 </ul>
 
 
 Acquired trainings in:
 
 
 <ul>
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 cGMP
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 Sterile &amp; aseptic techniques
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 Six Sigma.
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 QRM.
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 </ul>
 
 
 Must have knowledge:
 
 
 <ul>
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 Intermediate Knowledge of the general rules of good manufacturing practice,
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 Intermediate Knowledge of Six Sigma.
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 Background on solid &amp; sterile manufacturing techniques.
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 Awareness of TQM.
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 </ul>
 
 
</div>

Process Validation & Qualification expert

almulla holding llc

Position Title:Academic Quality Controller&#11835;Purpose of the Role:The Academic Quality Controller will ensure that all academic programs, teaching, assessment, and learning activities comply with institutional, national, and international standards. He / She is responsible for monitoring, evaluating, and continuously improving the quality of education delivery, curriculum design, faculty performance, and student outcomes.&#11835;Key Responsibilities1. Quality Assurance &amp; Compliance<ul><li>Develop, implement, and maintain academic quality assurance systems, policies, and procedures.</li><li>Ensure compliance with national accreditation bodies (e.g., Ministry of Education, CAA, or equivalent) and international accreditation standards (e.g., AACSB, EQUIS).</li><li>Conduct internal audits of academic departments, courses, and faculty performance.</li><li>Monitor adherence to institutional policies regarding assessment, grading, and academic integrity.</li></ul>2. Program Review &amp; Accreditation<ul><li>Coordinate periodic program reviews, self-evaluation reports (SER), and accreditation documentation.</li><li>Support academic departments during accreditation visits and audits.</li><li>Track action plans from external and internal review recommendations to ensure continuous improvement.</li></ul>3. Data Analysis &amp; Reporting<ul><li>Collect, analyze, and report data on academic performance, student outcomes, and faculty effectiveness.</li><li>Prepare reports for senior management and regulatory agencies on academic quality indicators (e.g., retention, graduation, student satisfaction).</li><li>Maintain academic quality dashboards or databases.</li></ul>4. Teaching &amp; Learning Enhancement<ul><li>Collaborate with faculty to promote best practices in teaching, assessment, and learning innovation.</li><li>Support curriculum development and revision based on data-driven evidence and feedback.</li><li>Organize workshops and training sessions on quality assurance and assessment practices.</li></ul>5. Stakeholder Engagement<ul><li>Liaise with deans, department heads, and faculty on quality improvement initiatives.</li><li>Engage students and alumni for feedback to improve program quality.</li><li>Communicate quality standards and outcomes across the institution.</li></ul>&#11835;Key Skills &amp; Competencies<ul><li>Deep understanding of higher education quality frameworks and accreditation standards.</li><li>Strong analytical, auditing, and report-writing skills.</li><li>Excellent organizational and project management abilities.</li><li>Attention to detail and ability to interpret academic regulations.</li><li>Communication and teamwork skills to collaborate across departments.</li><li>Proficiency in quality management systems, data analytics tools, or LMS reporting.</li></ul>&#11835;Qualifications<ul><li>Bachelor&rsquo;s degree in Education, Quality Management, or a related discipline (Master&rsquo;s preferred).</li><li>5+ years of experience in academic administration, quality assurance, or accreditation.</li><li>Familiarity with national (e.g., UAE CAA, QF Emirates) and international quality assurance standards.</li><li>Certification in quality management (ISO 9001, EFQM, or similar) is a plus.</li></ul>&#11835;Job Type: Full-timePay: AED10,000.00 - AED15,000.00 per monthApplication Question(s):<ul><li>How many years of experience do you have as Academic Quality Controller in a University or College in Dubai ?</li></ul>

Academic Quality Controller

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