engineering production worker

Hudson Manpower

<div><h2 class="jobSectionHeader">Job Summary</h2>
We are seeking an experienced Production Engineer with strong expertise in Steel Fabrication (Structural, Plates, and Piping) to manage and oversee fabrication activities for large-scale industrial projects including Refineries, Petrochemical plants, Fertilizer projects, and Storage Tank erection works. The candidate must have hands-on experience working with reputed contracting companies engaged in heavy fabrication and industrial construction projects.<h4 class="jobSectionHeader">
Client Interview in India in 1st week of March.</h4><h2 class="jobSectionHeader">
Key Responsibilities</h2><ul><li>
Plan, coordinate, and supervise fabrication activities for structural steel, plate works, piping spools, and storage tanks.</li><li>
Ensure production targets are achieved in line with project schedules and quality standards.</li><li>
Interpret engineering drawings, fabrication drawings, and isometric drawings accurately.</li><li>
Monitor material utilization and control wastage.</li><li>
Coordinate with QA/QC, Planning, Procurement, and Project teams for smooth workflow.</li><li>
Ensure compliance with international codes and standards (ASME, API, AWS, etc.).</li><li>
Supervise welding, cutting, rolling, assembly, and fit-up activities.</li><li>
Prepare daily production reports and progress updates.</li><li>
Optimize manpower deployment and shop floor efficiency.</li><li>
Ensure adherence to HSE standards and safe work practices.</li><li>
Support project team during inspections, audits, and client visits.</li><li>
Identify process improvements to enhance productivity and reduce fabrication cycle time.</li></ul> 
<ul><li>
Strong knowledge of Structural Steel Fabrication, Plate Fabrication, and Piping Fabrication.</li><li>
Experience in fabrication for Refineries, Petrochemical, Fertilizer plants, and Storage Tank erection projects.</li><li>
Familiarity with WPS, PQR, welding processes (SMAW, GTAW, GMAW, SAW).</li><li>
Understanding of NDT methods and quality control procedures.</li><li>
Ability to read and interpret technical drawings and material take-offs.</li><li>
Experience in production planning and scheduling.</li><li>
Strong leadership and team supervision skills.</li><li>
Good problem-solving and coordination abiliti</li></ul></div>

Production Engineer(Steel Fabrication) | UAE

AL BAWADI METAL INDUSTRIES LLS

We are looking for a dynamic and motivated Diploma Engineer to join our team.Position: Diploma Engineer Industry: Manufacturing Experience: 1&ndash;2 yearsKey Responsibilities:<ul><li>Assist in day-to-day engineering and technical activities</li><li>Prepare and maintain technical documents and reports</li><li>Coordinate with production / project / maintenance teams</li><li>Monitor work progress and ensure quality standards</li><li>Support installation, testing, and commissioning activities</li></ul>Requirements:<ul><li>Diploma in Mechanical / Electrical / Civil / relevant field</li><li>Basic technical and drawing knowledge</li><li>Familiarity with MS Office / AutoCAD (if required)</li><li>Good communication and teamwork skills</li></ul>Job Type: Full-timePay: AED3,500.00 - AED4,000.00 per month

Ast. Engineer Production

HARMAN India

<div>
 
 Introduction: A Career at HARMAN Automotive
 
 
 
 We&rsquo;re a global, multi-disciplinary team that&rsquo;s putting the innovative power of technology to work and transforming tomorrow. At HARMAN Automotive, we give you the keys to fast-track your career. Engineer audio systems and integrated technology platforms that augment the driving experience Combine ingenuity, in-depth research, and a spirit of collaboration with design and engineering excellence Advance in-vehicle infotainment, safety, efficiency, and enjoyment
 
 
 
 About The Role
 
 
 
 To ensure smooth, efficient, and high-quality production of automotive Connector Car and Car Audio products through effective planning, monitoring and optimization of the assembly lines, Act for implementation of production processes and procedures, leading productivity improvements, including new product introduction and manufacturing cell design to Reduce waste, Improve Safety, Quality, Delivery Performance. In this role, you will report to the Manager, Production and Operation.
 
 
 
 What You Will Do
 
 
 
 <ul>
 <li>
 Manage daily operations for assembly lines manufacturing Connected Car and Car Audio Products.
 </li>
 <li>
 Monitor production targets, cycle time and manpower planning to ensure output meets demand.
 </li>
 <li>
 Implement and maintain Standard Operating Procedures (SOPs) and Work Instructions (WI).
 </li>
 <li>
 Ensure compliance with IATF 16949, ISO 9001, ISO 14001, ISO 45001 and ESD standards.
 </li>
 <li>
 Coordinate with Quality and Engineering teams to address in-process defects, deviations, and audits.
 </li>
 <li>
 Support PPAP, FMEA, and root cause analysis (RCA) for production issues.
 </li>
 <li>
 Lead Kaizen and continuous improvement initiatives (Lean, 5S, Poka-Yoke, SMED).
 </li>
 <li>
 Drive improvements in OEE, Productivity and First Pass Yield (FPY).
 </li>
 <li>
 Optimize layout and workflow to reduce cycle time and waste.
 </li>
 <li>
 Monitor health and performance of assembly fixtures, jigs, tools and automated stations.
 </li>
 <li>
 Coordinate with maintenance for timely breakdown maintenance.
 </li>
 <li>
 Support NPI (New Product Introduction) and equipment validation activities.
 </li>
 <li>
 Train operators on new product assembly processes, safety, and quality norms.
 </li>
 <li>
 Ensure adherence to HARMAN&rsquo;s safety policies and promote a culture of zero harm.
 </li>
 <li>
 Supervise daily work and performance of line operators and contract workforce.
 
 
 </li>
 </ul>
 
 What You Need To Be Successful
 
 
 
 <ul>
 <li>
 Diploma/B.E./ B. Tech in Mechanical, Electronics, Electrical or related.
 </li>
 <li>
 Experience: 2&ndash;6 years in assembly operations within in automotive electronics.
 </li>
 <li>
 Familiar with PCBA Manufacturing process.
 </li>
 <li>
 Hands-on with SAP PP/MM, MS Office, and data reporting tools.
 </li>
 <li>
 Strong problem-solving, analytical thinking, team coordination and communication.
 
 
 </li>
 </ul>
 
 What Makes You Eligible
 
 
 
 <ul>
 <li>
 Be willing to travel up to domestic/International travel
 </li>
 <li>
 Be willing to work in office based on up dependencies
 
 
 </li>
 </ul>
 
 What We Offer
 
 
 
 <ul>
 <li>
 Flexible work environment, allowing for full-time remote work globally for positions that can be performed outside a HARMAN or customer location
 </li>
 <li>
 Access to employee discounts on world-class Harman and Samsung products (JBL, HARMAN Kardon, AKG, etc.)
 </li>
 <li>
 Extensive training opportunities through our own HARMAN University
 </li>
 <li>
 Competitive wellness benefits
 </li>
 <li>
 Tuition reimbursement
 </li>
 <li>
 &ldquo;Be Brilliant&rdquo; employee recognition and rewards program
 </li>
 <li>
 An inclusive and diverse work environment that fosters and encourages professional and personal development
 </li>
 </ul>
</div>

Junior Engineer, Production Assembly

ADNOC Group

<div>
 
 Job Purpose
 
 
 
 Manages and controls production process discipline aspects of all major works at sites from conception till implementation and handover to operations. Ensures all major works design and execution are in accordance with industry and company standards, practices and procedures
 
 
 Job Specific Accountabilities (Part 1)
 
 
 <ul>
 <li>
 Leads all major works from initiation till closeout to impart sites operational experience for development and execution of major works scope, goals and deliverables in line with company objectives and established procedures.
 </li>
 <li>
 Participates in review of lay outs, control schemes, specifications, O&amp;M studies, plot plan, 3D model Interface with engineering disciplines and provide inputs to carryout detailed engineering activities.
 </li>
 <li>
 Resolves technical &amp; execution issues which conflicts within the Major works execution plans, implementation and Site operations.
 </li>
 <li>
 Reviews &amp; comments at engineering packages for Major works comprising scope of work, data sheets, schedules, load lists, technical proposals, engineering estimates, startup and commissioning procedures as relevant.
 </li>
 <li>
 Manages and controls aspects of site execution in production and process discipline and support site management in ensuring safe operations to achieve sites production and injection targets.
 </li>
 <li>
 Identifies &amp; recommends solutions for interface problems between ongoing major works, existing plant and the sub systems and timely contribute towards minimizing changes to scope which might impact on cost and schedule for the major works.
 </li>
 <li>
 Establishes criteria and participate as required in site surveys, installation, pre-commissioning, commissioning and decommissioning of new projects, participate in troubleshooting. Provides technical advice &amp; assistance to plant operation on resolution of design.
 </li>
 <li>
 Coordinates with the site teams for optimum participation and involvement with major works expectations for successful and timely completion with backward integration and updates of major works developments to UZ site operations team.
 </li>
 <li>
 Develops Process Flow Diagrams (PFD), Piping and Instrument Diagrams (PID), Utility Flow Diagrams (UFD). Causes and effects tables of required design specifications and perform equipment sizing calculations and calculate line sizes and make flow summaries.
 </li>
 <li>
 Reviews technical proposals and engineering estimates and scope of work for the studies &amp; major works to be handled by outside Consultant or contractors.
 
 
 </li>
 </ul>
 Job Specific Accountabilities (Part 2)
 
 
 Job Specific Accountabilities (Part 3)
 
 
 Generic Accountabilities
 
 
 
 Supervision
 
 
 
 <ul>
 <li>
 Plan, supervise and coordinate all activities in the assigned area to meet functional objectives.
 </li>
 <li>
 Train and develop the assigned staff on relevant skills to enable them to become proficient on the job and deliver the respective section objectives.
 
 
 </li>
 </ul>
 
 Budgets
 
 
 
 <ul>
 <li>
 Provide input for preparation of the Department budgets and assist in the implementation of the approved Budget and work plans to deliver Section objectives.
 </li>
 <li>
 Investigate and highlight any significant variances to support effective performance and cost control.
 
 
 </li>
 </ul>
 
 Policies, Systems, Processes &amp; Procedures
 
 
 
 <ul>
 <li>
 Implement approved Section policies, processes, systems, standards and procedures in order to support execution of the Section&rsquo;s work programs in line with Company and International standards.
 </li>
 <li>
 Comply with all applicable legislation and legal regulations.
 
 
 </li>
 </ul>
 
 Performance Management
 
 
 
 <ul>
 <li>
 Contribute to the achievement of the approved Performance Objectives for the Section in line with the Company Performance framework.
 
 
 </li>
 </ul>
 
 Innovation and Continuous Improvement
 
 
 
 <ul>
 <li>
 Design and implement new tools and techniques to improve the quality and efficiency of operational processes.
 </li>
 <li>
 Identify improvements in internal processes against best practices in pursuit of greater efficiency in line with ISO standards in order to define intelligent solutions for issues confronting the function.
 
 
 </li>
 </ul>
 
 Health, Safety, Environment (HSE) and Sustainability
 
 
 
 <ul>
 <li>
 Comply with relevant HSE policies, procedures &amp; controls and applicable legislation and sustainability guidelines in line with international standards, best practices and ADNOC Code of Practices
 
 
 </li>
 </ul>
 
 Reports
 
 
 
 <ul>
 <li>
 Provide inputs to prepare Section MIS and progress reports for Company Management
 
 
 </li>
 </ul>
 Generic Accountabilities (continue)
 
 
 Internal Communications &amp; Working Relationships
 
 
 Contact with line Manager/ peers and other employees within the company/Group as required
 
 
 External Communications &amp; Working Relationships
 
 
 Contact with external parties including consultants, third party service providers, and government agencies as required
 
 
 Minimum Qualification
 
 
 Bachelors in Engineering
 
 
 
 Minimum Experience, Knowledge &amp; Skills
 
 
 
 6 years of experience
 
 
 Professional Certifications
 
 
 As applicable
 
 
 Work Condition, Physical effort &amp; Work Environment
 
 
 
 Physical Effort
 
 
 
 Minimal
 
 
 
 Work Environment
 
 
 
 A/C environment, could be exposed to the prevailing weather conditions like heat, humidity and dust during occasional site visits.
 
 
 Additional Details
 
 
 Job Family / Sub Family:Production Operations
</div>

Engineer, Production (Frac)

<div>We are seeking an experienced Machining Shop Skilled Worker to operate Plano Milling Machine and Horizontal Boring Machine (HBM) for machining large and heavy components as per engineering drawings and production requirements.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Operate Plano Miller and HBM machines independently</li><li>
Set up large workpieces, fixtures, and cutting tools</li><li>
Perform milling, boring, facing, drilling, and precision machining operations</li><li>
Read and interpret engineering drawings and tolerances</li><li>
Maintain dimensional accuracy and required surface finish</li><li>
Inspect components using measuring instruments</li><li>
Perform basic machine maintenance and troubleshooting</li><li>
Follow safety and quality standards</li></ul><ul><li>
Department: Production</li><li>
Division: Machining</li><li>
Category: Speciality Skilled Worker</li><li>
ITI Machinist (Mandatory)</li><li>
Milling Machine Certification (Mandatory)</li><li>
Minimum 6&ndash;8 years of experience in Plano Miller &amp; HBM operations</li><li>
Experience in machining large and heavy components</li><li>
Strong knowledge of cutting tools, feeds, and speeds</li><li>
Ability to read engineering drawings and maintain tight tolerances</li><li>
Hands-on experience with measuring instruments (Vernier, Micrometer, Bore Gauge, Dial Indicator, etc.)</li><li>
Understanding of shop floor safety standards</li><li>
Salary: SAR 2,500 &ndash; 3,500 + FAT (Food, Accommodation &amp; Transportation)</li></ul></div>

Machining Shop Skilled Worker – Plano Miller & HBM - Saudi Arabia

<div>We are seeking an experienced Machining Shop Skilled Worker to operate Horizontal Turning Lathe (HTL) and Vertical Turning Lathe (VTL) machines as per engineering drawings and production requirements. The candidate must ensure dimensional accuracy and quality compliance.<h3 class="jobSectionHeader">
Key Responsibilities</h3><ul><li>
Operate HTL / VTL machines as per drawing specifications</li><li>
Set up machine parameters and tooling</li><li>
Perform machining operations including turning, facing, boring, and threading</li><li>
Read and interpret engineering drawings and tolerances</li><li>
Check dimensions using measuring instruments</li><li>
Maintain machine cleanliness and perform basic maintenance</li><li>
Follow safety and quality standards</li><li>
Coordinate with supervisor and quality department</li></ul><ul><li> 
Department: Production</li><li>
Division: Machining</li><li>
Category: Speciality Skilled Worker</li><li>
ITI Machinist (Mandatory)</li><li>
CNC / Lathe Machine Certification</li><li>
Minimum 6&ndash;8 years of experience in HTL / VTL machining</li><li>
Strong knowledge of machining parameters and tooling</li><li>
Ability to read engineering drawings and maintain tolerances</li><li>
Hands-on experience with measuring instruments (Vernier, Micrometer, Bore Gauge, etc.)</li><li>
Understanding of shop floor safety standards</li><li>
Salary: SAR 2,500 &ndash; 3,500 + FAT (Food, Accommodation &amp; Transportation)</li></ul></div>

Machining Shop Skilled Worker – HTL / VTL - Saudi Arabia

Amerikan Hastanesi

<div>
 
 Stembio (
 
 Ko&ccedil; Holding/Ko&ccedil; Healthcare
 
 i&scedil;tiraki),
 
 Mezenkimal K&ouml;k H&uuml;creler (MSC), Eksozomlar, &Idot;mm&uuml;noterapi &Uuml;r&uuml;nleri, Kordon Kan&inodot; Bankalama ve Doku Greftleri
 
 &uuml;retimi ve haz&inodot;rlanmas&inodot; konusunda uzmanla&scedil;m&inodot;&scedil;, ileri teknolojiye sahip bir
 
 cGMP laboratuvar&inodot;d&inodot;r
 
 . Kalite kontrol ve validasyon s&uuml;re&ccedil;lerine b&uuml;y&uuml;k &ouml;nem vererek,
 
 y&uuml;ksek kaliteli ve reg&uuml;lasyonlara uygun
 
 h&uuml;cresel tedavi &uuml;r&uuml;nleri sunmay&inodot; taahh&uuml;t ediyoruz.
 
 
 
 
 
 Farkl&inodot; kaynaklardan mezenkimal k&ouml;k h&uuml;crelerin &uuml;retimi, imm&uuml;noterapi &uuml;r&uuml;nleri (sitokinle ind&uuml;klenmi&scedil; &ouml;ld&uuml;r&uuml;c&uuml; h&uuml;creler, dendritik h&uuml;creler), fibroblast h&uuml;crelerinin &uuml;retimi ve h&uuml;cre k&uuml;lt&uuml;r&uuml; s&uuml;re&ccedil;lerinin takibi ve &uuml;r&uuml;n haz&inodot;rlanmas&inodot;nda g&ouml;rev alacak,
 
 Stembio
 
 'da g&ouml;revlendirilmek &uuml;zere kalifiye ve deneyimli bir
 
 &Uuml;retim Personeli
 
 ar&inodot;yoruz.
 
 
 
 
 
 E&gbreve;er
 
 ileri h&uuml;cresel tedavilerde kalite kontrol&uuml;ne tutkuyla ba&gbreve;l&inodot;ysan&inodot;z
 
 ve en y&uuml;ksek standartlar&inodot; koruma konusunda yetkin oldu&gbreve;unuzu d&uuml;&scedil;&uuml;n&uuml;yorsan&inodot;z, ba&scedil;vurunuzu bekliyoruz!
 
 
 
 
 
 
 Genel Nitelikler
 
 
 
 
 
 <ul>
 <li>
 Biyoloji, Biyom&uuml;hendislik, Biyoteknoloji, Molek&uuml;ler Biyoloji veya ilgili bir alanda en az Y&uuml;ksek Lisans mezunu,
 </li>
 <li>
 Tercihen iyi seviyede &Idot;ngilizce dil bilgisi bulunan (okuma ve yazma),
 </li>
 <li>
 cGMP d&uuml;zenlemelerine tabi bir &uuml;retim ortam&inodot;nda en az 2 y&inodot;l ve &uuml;zeri deneyimi bulunan (tercihen h&uuml;cresel tedavi, rejeneratif t&inodot;p veya biyofarmas&ouml;tik sekt&ouml;rlerinde),
 </li>
 <li>
 H&uuml;cre izolasyonu (mezenkimal k&ouml;k h&uuml;cre vb.), h&uuml;cre pasajlanmas&inodot;, h&uuml;cre dondurma, h&uuml;cre k&uuml;lt&uuml;r&uuml; takibi konular&inodot;nda pratik deneyimi bulunan,
 </li>
 <li>
 Validasyon protokollerini &uuml;r&uuml;n&uuml;n geli&scedil;tirilmesi y&ouml;n&uuml;nde etkin bir &scedil;ekilde planlama, planlanan s&uuml;re&ccedil;lerin takibi, raporlanmas&inodot; konular&inodot;nda g&uuml;&ccedil;l&uuml; bilgisi bulunan,
 </li>
 <li>
 Reg&uuml;latif gereklilikler (FDA, EMA, T&Idot;TCK, ICH k&inodot;lavuzlar&inodot;) ve kalite y&ouml;netim sistemleri (QMS) konusunda deneyimi bulunan,
 </li>
 <li>
 Analitik d&uuml;&scedil;&uuml;nme, problem &ccedil;&ouml;zme yetenekleri g&uuml;&ccedil;l&uuml; olan,
 </li>
 <li>
 Ekip &ccedil;al&inodot;&scedil;mas&inodot;na uygun bir &scedil;ekilde planlamalar yaparak s&uuml;reci y&ouml;netme yetkinli&gbreve;i bulunan,
 </li>
 <li>
 Dok&uuml;mantasyon, raporlama ve sunum yapma konusunda ileti&scedil;im becerileri g&uuml;&ccedil;l&uuml; olan,
 </li>
 </ul>
 
 
 
 
 
 Rol ve Sorumluluklar
 
 
 
 
 
 <ul>
 <li>
 &Idot;yi &Uuml;retim Uygulamalar&inodot; (GMP) standartlar&inodot;na uygun &ccedil;al&inodot;&scedil;mak, B s&inodot;n&inodot;f &uuml;retim odalar&inodot;nda &uuml;retim s&uuml;re&ccedil;lerini y&uuml;r&uuml;tmek,
 </li>
 <li>
 &Ccedil;e&scedil;itli dokulardan mezenkimal k&ouml;k h&uuml;crelerin izolasyonunu yapmak,
 </li>
 <li>
 Mezenkimal k&ouml;k h&uuml;crelerin h&uuml;cre k&uuml;lt&uuml;r&uuml;nde takibini yapmak ve h&uuml;creleri &ccedil;o&gbreve;altmak,
 </li>
 <li>
 T h&uuml;cre ve dentritik h&uuml;cre k&uuml;lt&uuml;rlerinde aktif g&ouml;rev almak,
 </li>
 <li>
 Ba&gbreve;&inodot;&scedil;&inodot;kl&inodot;k sistemi h&uuml;crelerinin &uuml;retim s&uuml;re&ccedil;lerinde g&ouml;rev almak,
 </li>
 <li>
 Y&ouml;ntem geli&scedil;tirmeye katk&inodot;da bulunmak, ara&scedil;t&inodot;rmak ve bunun uygulanmas&inodot; i&ccedil;in validasyon &ccedil;al&inodot;&scedil;malar&inodot;n&inodot; ger&ccedil;ekle&scedil;tirmek,
 </li>
 <li>
 T&uuml;m s&uuml;re&ccedil;lerin dok&uuml;mantasyonunda g&ouml;rev almak; SOP, protokoller ve raporlar&inodot; reg&uuml;lasyona uygun &scedil;ekilde yazmak,
 </li>
 <li>
 cGMP, EMA, T&Idot;TCK ve di&gbreve;er reg&uuml;lasyonlara uygunlu&gbreve;u sa&gbreve;lamak,
 </li>
 <li>
 T&uuml;m &uuml;retim s&uuml;re&ccedil;lerinde al&inodot;nan kalite kontrol verilerini incelemek, s&uuml;recin geli&scedil;tirilmesine katk&inodot;da bulunmak,
 </li>
 <li>
 Sapmalar&inodot;, spesifikasyon d&inodot;&scedil;&inodot; (OOS) sonu&ccedil;lar&inodot; ve uygunsuzluklar&inodot; ara&scedil;t&inodot;rmak, gerekli d&uuml;zeltici ve &ouml;nleyici faaliyetleri (CAPA) uygulamak,
 </li>
 <li>
 S&uuml;recin devaml&inodot;l&inodot;&gbreve;&inodot;n&inodot; sa&gbreve;lamak i&ccedil;in uygun planlama ve ekip &ccedil;al&inodot;&scedil;mas&inodot;n&inodot; ger&ccedil;ekle&scedil;tirmek,
 </li>
 <li>
 H&uuml;cresel &uuml;r&uuml;nlerin &uuml;retim s&uuml;re&ccedil;lerinin y&uuml;r&uuml;t&uuml;lmesi,
 </li>
 <li>
 Proses validasyonlar&inodot;na kat&inodot;l&inodot;m sa&gbreve;lamak,
 </li>
 <li>
 cGMP, reg&uuml;lasyonlar ve &scedil;irket standartlar&inodot;na uygunlu&gbreve;u sa&gbreve;lanmak,
 </li>
 </ul>
 
 
 
 
 
 Ki&scedil;isel verileriniz, i&scedil; ba&scedil;vurunuzun al&inodot;nmas&inodot; ve de&gbreve;erlendirmesi amac&inodot;yla i&scedil;lenmektedir. &Idot;&scedil;lenen ki&scedil;isel verilerinize ve haklar&inodot;n&inodot;za ili&scedil;kin detayl&inodot; bilgilere websitemizin &ldquo;&Idot;nsan Kaynaklar&inodot;&rdquo; ba&scedil;l&inodot;&gbreve;&inodot; i&ccedil;erisinde yer alan&ldquo;&Ccedil;al&inodot;&scedil;an Aday&inodot; Ayd&inodot;nlatma Metni&rsquo;nden ula&scedil;abilirsiniz.
 
 
 
 
 
 
 -------------------------------------------------------------------------------------------------------------
 
 
 
 
 
 Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of 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 qualified and experienced
 
 Production Personnel for Stembio
 
 to be responsible for the production of mesenchymal stem cells from various sources, immunotherapy products (cytokine-induced killer cells, dendritic cells), fibroblast cell production, and monitoring of cell culture processes and product preparation.
 
 
 
 
 
 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>
 A minimum of a Master&rsquo;s degree in Biology, Biomedical Engineering, Biotechnology, Molecular Biology, or a related field.
 </li>
 <li>
 Proficiency in English is a plus
 </li>
 <li>
 At least 2+ years of experience in a cGMP-regulated production environment (preferably in the fields of cell therapy, regenerative medicine, or biopharmaceuticals).
 </li>
 <li>
 Hands-on experience in cell isolation (e.g., mesenchymal stem cells), cell passaging, cell freezing, cell culture monitoring.
 </li>
 <li>
 Strong knowledge in planning validation protocols effectively for product development, tracking planned processes, and reporting outcomes.
 </li>
 <li>
 Experience with regulatory requirements (FDA, EMA, T&Idot;TCK, ICH guidelines) and quality management systems (QMS).
 </li>
 <li>
 Analytical thinking, problem-solving skills.
 </li>
 <li>
 Ability to manage the process by planning effectively within a team-oriented environment.
 </li>
 <li>
 Strong communication skills in documentation, reporting, and presentation.
 </li>
 </ul>
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 <ul>
 <li>
 Work in compliance with Good Manufacturing Practices (GMP) standards and execute production processes in Class B manufacturing rooms.
 </li>
 <li>
 Isolate mesenchymal stem cells from various tissues.
 </li>
 <li>
 Monitor mesenchymal stem cells in culture and expand them.
 </li>
 <li>
 Actively participate in T cell and dendritic cell cultures and contribute to the production processes of immune system cells.
 </li>
 <li>
 Contribute to method development, conduct research, and perform validation studies for implementation.
 </li>
 <li>
 Take part in the documentation of all processes; write SOPs, protocols, and reports in compliance with regulations.
 </li>
 <li>
 Ensure compliance with cGMP, EMA, T&Idot;TCK, and other relevant regulations.
 </li>
 <li>
 Review quality control data collected from all production processes and contribute to process improvement.
 </li>
 <li>
 Investigate deviations, out-of-specification (OOS) results, and non-conformities, and implement necessary corrective and preventive actions (CAPA).
 </li>
 <li>
 Ensure process continuity through proper planning and teamwork.
 </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 - Hücresel Ürünler - Üretim Personeli / Manufacturing Personnel

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