19 Vehicle Testing jobs in the United Arab Emirates

Dicetek LLC is seeking a detail-oriented and innovative IT ATM Test Engineer to join our team in Abu Dhabi. This role offers an exciting opportunity for professionals interested in ATM technology and IT testing processes. As an IT ATM Test Engineer, you will play a crucial role in ensuring the quality and functionality of ATM systems, supporting our mission of delivering seamless, secure, and efficient banking solutions.

Develop, execute, and document comprehensive test plans for ATM systems.
Conduct functional, regression, and system integration testing to ensure optimal performance.
Identify, analyze, and resolve defects and issues in collaboration with development teams.
Maintain and update test environments to support various project phases.
Ensure compliance with security standards and best practices in ATM testing.
Collaborate with cross-functional teams to meet project requirements and timelines.
Provide detailed reports on testing outcomes, metrics, and improvement opportunities.

Proficient in ATM Switches (Base24 eps), ISO Messages, data structures, Visa and MasterCard Interfaces.
In-depth knowledge of cards (Debit, Credit, Pre-paid), issuing and acquiring payments, Switching and transaction routing, Merchant Management, ATM, POS terminals, and Banking Kiosks.
Experience with ATMs (NCR, Diebold), ATM Message protocols (NDC, IFX, ATM Web Interfaces), Cash Deposit machines, Cash recyclers, ATM flow and state management, ATM Experience Management (NCR Connections, Aptra Activate, Wincor Proflex), Anti Skimming, HSM (Thales, Safenet), and Key management.
Knowledge of smart and non-smart card solutions, Chip Payment (EMV) Technology, EMV developments and trends.
Understanding of MasterCard/Visa Payment systems specifications, ISO Message interfaces, file handling, and security key management.
Knowledge of payment gateway systems and solutions, 3DSecure/SecureCode specifications and interfaces.
Understanding of ATM/EFTPOS terminals, secure communications and solutions.
Knowledge of Payment Card Industry (PCI) and Payments Applications Security Standards.
Familiarity with Card and Chip Personalization Systems and host interfaces, and instant personalization solutions.

At Dicetek LLC, we are passionate about delivering innovative IT solutions that empower businesses to excel in the digital age. With a focus on excellence, integrity, and client satisfaction, we specialize in providing cutting-edge technology services tailored to diverse organizational needs. As a leader in the IT industry, we foster a culture of innovation, collaboration, and continuous growth. Learn more about us at dicetek.net or follow us on LinkedIn.

Wanna join the adventure?

As we embark on designing, producing, and operating cutting-edge satellites, we are seeking a skilled and versatile Test Infrastructure Engineer to design, build, and maintain the systems that power our hardware and software verification and validation. You will own the development of test benches and test stations — from concept through delivery and ongoing support — enabling our teams to integrate, validate, and deliver satellite systems at scale.

This is a unique opportunity to shape the backbone of our testing operations in a fast-paced, high-tech environment where every improvement you make directly accelerates our mission. This role requires someone who is highly technical, detail-oriented, and thrives on solving complex, cross-disciplinary challenges — all while bringing a mindset of standardization, automation, and continuous improvement to every project.

• Test Bench & Test Station Development
• Design, build, and maintain software-in-the-loop (SIL) and hardware-in-the-loop (HIL) test benches to support satellite hardware and software validation.
• Own updates, evolution, and lifecycle management of test infrastructure to support current and future programs.
• Maintain and improve test stations, tools, and equipment for integration and test (I&T) campaigns.
• Cross-Functional Collaboration
• Work closely with Systems, AIT, Software, and Product teams from design to execution, ensuring test infrastructure meets program objectives.
• Support AIT campaigns with test setup, troubleshooting, and automation improvements.
• Process & Tooling Improvement
• Refine and standardize tools, processes, and interfaces involved in test infrastructure.
• Automate repetitive tasks and improve dynamicity in test workflows.
• Contribute to company-level process definitions to meet Orbitworks’ scaling goals.
• Stakeholder Interaction
• Act as the point of contact for test infrastructure needs, working closely with engineering teams to prioritize and deliver solutions.
• Identify pain points and propose actionable improvements to increase efficiency and reliability.

• 5+ years of experience working with Linux and networking fundamentals.
• Hands-on experience with embedded hardware (Engineering Models, Flight Models).
• Proven track record in system validation and platform integration.
• Strong debugging skills for Linux system management (systemd, networkd, file systems) and HIL setups.
• Solid understanding of VLANs, OSI layers, packet tracing, TCP/UDP protocols, and network diagnostics tools (tcpdump, Wireshark).
• Proficient in Python and scripting languages (e.g., bash).
• Skilled with software development practices, version control (git, GitLab), and containerization (Docker, pods).
• Experience with continuous integration tools and cloud-based automation.
• Familiarity with Manufacturing Execution Systems (MES), Product Lifecycle Management (PLM), and procurement processes.

• Deep understanding of embedded and space protocols and standards.
• Experience collaborating with mechanical and electrical engineering teams.
• Knowledge of harness design and build.
• Additional programming languages (C, C++, C#, Lua, YAML, Cue).
• Experience setting up automated HIL test benches.
• Previous work with space systems.

Orbitworks' mission is to make space simple for organizations that want to deploy physical and virtual missions to space. Building on Loft Orbital's heritage, Orbitworks will be the first commercial firm in the United Arab Emirates to mass-manufacture satellites. Orbitworks aims to manufacture tens of satellites annually and operates out of a 50,000-square-foot facility in Abu Dhabi.

Responsibilities

• Minimum 5 years experience in Quality department (Quality assurance and Quality control activities, Auditing (External and Internal), QMS Documentation)
• QMS Lead Auditor (ISO 9001/AS 9100)
• Experienmce and knowledge in 8D, Root Cause Analysis , Corrective actions effectiveness assessment, PPAP
• TO monitor overall Quality Assurance activities
• Supplier quality improvement programs
• NCR , SCAR handling
• Emnsuring compliance of all process to Quality system procedure requirements
• Develop and execute comprehensive test plans and test cases for automotive systems, ensuring thorough coverage of all requirements and functionalities to guarantee product quality.
• Conduct in-depth audits of automotive manufacturing processes, identifying areas of non-compliance with industry standards
• Collaborate closely with cross-functional teams (e.g., design, engineering, manufacturing) to resolve quality issues, implement improvements, and promote a culture of quality throughout the product lifecycle.
• Perform root cause analysis of defects and failures, utilizing various analytical tools and techniques to determine the underlying causes and prevent recurrence.
• Lead and participate in product testing and validation activities,
• Monitor and evaluate supplier quality performance, conducting audits and assessments to ensure compliance with quality standards and specifications.
• Prepare detailed quality reports, including test results, defect analysis, and audit findings, to communicate quality performance to stakeholders and facilitate data-driven decision-making.
• Stay abreast of the latest automotive industry trends, technologies, and quality standards to continuously improve testing methodologies and auditing practices.
• Drive continuous improvement initiatives, identifying and implementing process improvements to enhance product quality, reduce defects, and optimize efficiency within the organization.

Join our blockchain team to work on large-scale projects with a focus on R&D, coding, and QA. Requires Java/Python proficiency, automation testing, and fluency in English/Mandarin.

Overview:

Our blockchain team is expanding. Join our innovative team and contribute to driving impactful projects in a dynamic and fast-paced environment!

Strong development skills with some hands-on experiences on automation testing; Good opportunity to work on big scale in-house development projects for the cryptocurrency exchange platform; End-to-end development on R&D, coding, DevOps, and Quality Assurance.

Job Responsibilities:

1. Participate in the review of product requirements, system design, and program code, and provide improvement suggestions.
2. Design and execute test cases to track and locate defects or issues in product software.
3. Propose a reasonable automation solution based on product and project characteristics, and be responsible for designing and implementing automated testing tools to improve testing efficiency.
4. Improve the existing testing plan to enhance testing quality, including testing process improvement, testing innovation, and the introduction of new testing methods.

Job Requirements:

1. Experience in large-scale system project development or Quality Assurance, familiar with the software R&D process, and possess systematic development/testing analysis and design capabilities.
2. Proficient in Java/Python and other languages, with more than 5 years of relevant development/SAST white-box testing experience, familiar with commonly used design patterns.
3. Experienced in engineering development, familiar with the design and development of common database products; designed and implemented test platforms, DevOps, etc., with in-depth understanding of Quality Assurance.
4. Strong interest in technology, attention to cutting-edge technologies, and good research skills.
5. Fluency in English and Mandarin is a must.

Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.

We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC

Quality Control Analyst will be responsible for performing analytical testing, maintaining laboratory resources, ensuring compliance with quality and safety standards, and supporting product release, method transfers, and validations. He /She will work with advanced analytical instruments, uphold data integrity principles, and ensure full compliance with GMP requirements to maintain product quality, safety, and efficacy.

Job Responsibilities

• Perform analysis of raw materials, packaging materials, bulk products, finished products, in-process samples, stability samples, process/cleaning validation samples, and miscellaneous samples as per approved methods and protocols.
• Ensure all activities comply with GLP, GMP, and ALCOA+ principles.
• Operate major analytical instruments including HPLC, GC, Dissolution Apparatus, UV-Vis Spectrophotometer, and IR.
• Perform daily verification, calibration, and routine maintenance of instruments as per SOPs.
• Maintain an up-to-date inventory of reference standards, working standards, impurity standards, analytical columns, reagents, chemicals, and consumables.
• Conduct qualification of working standards against reference or primary standards.
• Prepare volumetric solutions and standardize them for routine use.
• Prepare, review, and update SOPs, test methods, and specifications as needed.
• Record all data accurately, clearly, and in real-time following GLP requirements.
• Report and support investigations for any OOS, OOT, incidents, or non-compliance activities.
• Initiate and support Change Control, CAPA, and Deviation processes as required.
• Follow safety procedures and use the recommended PPE for all QC activities.
• Ensure compliance with EHS policies and safe work practices in the laboratory.
• Support analytical validation/verification and cleaning validation studies.
• Participate in laboratory improvement initiatives.
• Carry out additional tasks assigned by the QC Manager in line with department objectives.

Qualifications & Skills:

• Bachelor’s degree in chemistry, pharmaceutical sciences, or related discipline.
• 1–3 years of experience in a pharmaceutical QC laboratory.
• Hands-on experience with HPLC, GC, Dissolution, UV, and IR instruments.
• Knowledge of LIMS and SAP systems is preferred.
• Good understanding of GMP, GLP, and data integrity principles (ALCOA+).
• Strong attention to detail, analytical thinking, and problem-solving skills.
• Effective communication and teamwork abilities.

This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!

Please apply via our HR system here.

Quality Control – Document Administrator

Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.

We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality Control team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC

Job Overview:

The QC Document Administrator is responsible for ensuring effective control of all QC documentation and sample management processes, in alignment with GLP, GMP, and data integrity principles, supporting laboratory compliance, resources coordination, and ensures smooth execution of QC operations from material receipt to reporting.

Job Responsible:

• Manage QC documents (SOPs, specifications, STPs, release reports, logbooks, training records) in compliance with ALCOA+ principles.
• Ensure timely drafting, revision, approval, and archival of SOPs, specifications, standard test procedures, and reports.
• Maintain document storage, retrieval, and archival systems (manual and electronic such as SAP, Dot Compliance, etc.).
• Monitor document version control and ensure accessibility to authorized personnel only.
• Oversee receipt, registration, and distribution of QC samples as per lot management and sample receiving procedures.
• Ensure proper handling, storage, and tracking of samples (raw materials, packaging, intermediates, finished products, and stability).
• Performing sampling activities for raw materials and water system samples in compliance with GLP and SOPs.
• Maintain sample retention and disposal records as per regulatory and company requirements.
• Monitor and reinforce adherence to GLP practices within the QC laboratory.
• Support internal audits, inspections, and compliance activities by ensuring availability and accuracy of records.
• Report and escalate any observed deviations, non-compliance, or data integrity concerns to QC Manager.
• Coordinate usage and availability of sampling and testing resources (sampling tools, logbooks, controlled forms, etc.).
• Support QC Manager in managing laboratory schedules, prioritizing sample workflows, and aligning resources for timely completion.
• Ensure laboratory personnel training records are maintained, up-to-date, and available for audits.
• Ensure all activities are performed in compliance with EHS policy and PPE requirements.
• Maintain strict confidentiality of QC data, documents, and product information.
• Participate in improvement initiatives for QC operations and documentation processes.
• Provide inputs for system enhancements (SAP, LIMS, documentation tools) to streamline QC efficiency.
• Perform any other responsibilities assigned by the QC Manager to support department needs.

Qualifications & Skills:

• Bachelor’s degree in science or pharmacy with relevant experience.
• 1-3 years of experience in pharmaceutical QC role (GLP/GMP environment preferred).
• Knowledge of data integrity (ALCOA+), GLP, and regulatory requirements.
• Strong organizational skills, attention to detail, and ability to manage multiple priorities.
• Familiarity with SAP, LIMS, or other digital quality/document management systems is an advantage.

This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!

Only direct applications will be considered. Please apply via our HR system here.

Job Overview

The QC Document Controller is responsible for ensuring effective control of all QC documentation and sample management processes, in alignment with GLP, GMP, and data integrity principles, supporting laboratory compliance, resources coordination, and ensures smooth execution of QC operations from material receipt to reporting.

• Manage QC documents (SOPs, specifications, STPs, release reports, logbooks, training records) in compliance with ALCOA+ principles.
• Ensure timely drafting, revision, approval, and archival of SOPs, specifications, standard test procedures, and reports.
• Maintain document storage, retrieval, and archival systems (manual and electronic such as SAP, Dot Compliance, etc.).
• Monitor document version control and ensure accessibility to authorized personnel only.
• Oversee receipt, registration, and distribution of QC samples as per lot management and sample receiving procedures.
• Ensure proper handling, storage, and tracking of samples (raw materials, packaging, intermediates, finished products, and stability).
• Perform sampling activities for raw materials and water system samples in compliance with GLP and SOPs.
• Maintain sample retention and disposal records as per regulatory and company requirements.
• Monitor and reinforce adherence to GLP practices within the QC laboratory.
• Support internal audits, inspections, and compliance activities by ensuring availability and accuracy of records.
• Report and escalate any observed deviations, non-compliance, or data integrity concerns to QC Manager.
• Coordinate usage and availability of sampling and testing resources (sampling tools, logbooks, controlled forms, etc.).
• Support QC Manager in managing laboratory schedules, prioritizing sample workflows, and aligning resources for timely completion.
• Ensure laboratory personnel training records are maintained, up-to-date, and available for audits.
• Ensure all activities are performed in compliance with EHS policy and PPE requirements.
• Maintain strict confidentiality of QC data, documents, and product information.
• Participate in improvement initiatives for QC operations and documentation processes.
• Provide inputs for system enhancements (SAP, LIMS, documentation tools) to streamline QC efficiency.
• Perform any other responsibilities assigned by the QC Manager to support department needs.

• Bachelor’s degree in science or pharmacy with relevant experience.
• 1-3 years of experience in pharmaceutical QC role (GLP/GMP environment preferred).
• Knowledge of data integrity (ALCOA+), GLP, and regulatory requirements.
• Strong organizational skills, attention to detail, and ability to manage multiple priorities.
• Familiarity with SAP, LIMS, or other digital quality/document management systems is an advantage.

This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!

Please apply via our HR system here.

The Quality Control Specialist will be responsible for ensuring that all joinery products (kitchens, wardrobes, doors, custom furniture, and other wood products) meet high standards of craftsmanship, durability, and finish. This role involves setting up inspection systems, monitoring production at every stage, and ensuring compliance with design specifications, material standards, and client expectations.

• Develop and implement quality control checklists and procedures for joinery production (cutting, assembly, finishing, installation).
• Inspect raw materials (wood, veneers, laminates, hardware, fittings) for quality and conformity with approved specifications.
• Conduct in-process inspections to monitor dimensions, joints, finishing, and surface treatments.
• Approve/reject products based on tolerance, appearance, and durability standards.
• Ensure packaging, handling, and site delivery are done in accordance with QC protocols.

• Maintain compliance with ISO, FSC, and local standards relevant to joinery and interiors.
• Identify recurring defects and coordinate with production supervisors for corrective and preventive actions.
• Ensure adherence to project drawings, shop drawings, and specifications before release for client approval.
• Work closely with installation teams to ensure site execution matches factory QC standards.

• Maintain QC records, inspection reports, and NCRs (Non-Conformance Reports).
• Provide feedback loops to the design, procurement, and production teams.
• Prepare weekly QC reports for management and project stakeholders.
• Train production and installation staff on quality standards and best practices.
• Support the Management in client handover inspections.
• Participate in continuous improvement initiatives across the production floor.

• Minimum 3–5 years of proven QC experience in joinery/interiors/kitchen & wardrobe production.
• Strong knowledge of joinery techniques, woodworking machinery, finishes, and hardware systems (hinges, slides, fittings, accessories).
• Familiarity with AutoCAD/technical drawings and ability to read detailed shop drawings.
• Understanding of ISO standards, quality management systems, and inspection protocols.
• Excellent attention to detail and problem-solving ability.
• Strong communication and documentation skills (English essential, Arabic and Hindi is a plus).

Overview

Specialism Quality Control / Inspection / HSE

The Quality Control Engineer – Instrumentation & Control (I&C) is responsible for overseeing the inspection and testing of instrumentation and control systems to ensure they comply with project specifications, codes, and safety standards. This role involves conducting functional tests, reviewing documentation, and identifying any defects or deviations during installation and commissioning phases. The engineer collaborates with project teams to implement corrective measures and ensure system reliability. In addition to field inspections, the Quality Control Engineer supports quality assurance activities, participates in audits, and maintains accurate records of quality performance. Strong technical knowledge of I&C systems, attention to detail, and effective communication skills are critical to ensuring the delivery of fully functional and compliant control systems.

• Oversee inspection and testing of instrumentation and control systems to ensure compliance with project specifications, codes, and safety standards.
• Perform functional tests, review documentation, and identify defects or deviations during installation and commissioning.
• Collaborate with project teams to implement corrective measures and ensure system reliability.
• Support quality assurance activities, participate in audits, and maintain accurate records of quality performance.

• Bachelor’s degree in Electrical, Instrumentation, Control, or related engineering discipline
• 5+ years of experience in instrumentation and control quality control, preferably in oil & gas, power generation, or industrial projects
• In-depth knowledge of I&C systems, instrumentation calibration, loop checks, and functional testing
• Familiarity with relevant standards and codes (ISA, IEC, API)
• Ability to interpret I&C drawings, P&IDs, and technical specifications
• Strong problem-solving skills and attention to detail
• Effective communication and teamwork abilities
• Experience in commissioning and system handover processes is a plus