validation engineer

Lennox International

<div><div><b>Lennox (NYSE: LII)</b> Driven by 130 years of legacy, HVAC and refrigeration success, Lennox provides our residential and commercial customers with industry-leading climate-control solutions. At Lennox, we win as a team, aiming for excellence and delivering innovative, sustainable products and services. Our culture guides us and creates a workplace where all employees feel heard and welcomed. Lennox is a global community that values each team member&rsquo;s contributions and offers a supportive environment for career development. Come, stay, and grow with us.</div><p><b><i><br>
Innovate your career.</i></b></p><p></p><p><br>
When you choose Lennox, you're getting the best.</p><p></p><p><br>
When you work at Lennox, you&rsquo;re among the best.</p><p></p><p>
Lennox is seeking a highly skilled and experienced <b>Software Systems Validation Engineer</b> to join our team in <b>Carrollton, TX. </b>This role focuses on the validation of embedded controllers that power innovative HVAC solutions for commercial applications.</p><p></p><p><br>
As a key member of the validation team, the selected candidate will be responsible for ensuring the quality, reliability, and robustness of embedded HVAC controller systems. The role involves validating complex system interactions across hardware, firmware, and communication layers. It requires a proactive, hands-on engineer with the ability to thrive in fast-paced environments, adapt to dynamic project requirements, and deliver results under constrained timelines.</p><p></p><p><b><br>
DUTIES INCLUDE BUT ARE NOT LIMITED TO:</b></p><br>
<p></p><ul><li>
Design and develop comprehensive validation strategies tailored for embedded controllers in the HVAC domain.</li><li>
Create and maintain test deliverables, including:
</li><li><ul><li>Test plans aligned with project requirements and functional specifications.</li><li>
Test content such as manual and automated test cases for validating system functionality, performance, and reliability.</li><li>
Test execution schedules, ensuring all test activities are performed on time.</li><li>
Bug reports with detailed root cause analysis and actionable feedback for development teams.</li><li>
Test reports summarizing results, coverage, and overall system quality.</li></ul></li><li>
Execute validation activities across all stages of the Software Testing Life Cycle (STLC), ensuring system compliance with functional, performance, and reliability requirements.</li><li>
Collaborate with cross-functional teams, including software developers, system architects, hardware engineers, and product managers, to define test requirements, align on deliverables, and resolve issues.</li><li>
Develop and maintain automated test solutions to enhance coverage, efficiency, and repeatability of validation processes.</li><li>
Debug and troubleshoot complex interactions between hardware and software, utilizing tools like oscilloscopes, logic analyzers, and protocol analyzers.</li><li>
Contribute to continuous improvement efforts in validation methodologies, tools, and processes to elevate quality standards.</li><li>
Ensure alignment with project schedules, consistently meeting deadlines with minimal supervision while maintaining high-quality standards.</li></ul><div>
#LI-onsite #LI-JM1</div><p><b><i><br>
Required:</i></b></p><ul><li>
Bachelor&rsquo;s or Master&rsquo;s degree in Electronics Engineering, Computer Science, or a related field.</li><li>
Minimum 5 years of professional experience in system-level validation, ideally in embedded systems.</li><li><b>
Strong understanding of embedded systems, including microcontrollers, real-time operating systems (RTOS), and firmware development.</b></li><li>
Proficiency in debugging and troubleshooting hardware/software interfaces.</li><li>
Expertise in validation tools, automation frameworks, and scripting languages <b><i>(Python preferred)</i></b>.</li><li>
Familiarity with communication protocols such as UART, I2C, SPI, CAN, BLE.</li></ul><p><b><i>
Preferred:</i></b></p><ul><li>
Familiarity with programming languages such as C, C++, C#, and scripting languages like Python, bash, Rust.</li><li>
Experience validating systems in industries such as HVAC, automotive, aerospace, medical, industrial controls, or related fields.</li><li>
Hands-on experience with test management tools, Azure DevOps preferred.</li><li>
Expertise with Version control tools, preferably Git, and knowledge of CI/CD pipelines for continuous integration and deployment is a plus.</li></ul><p><b><i>
Soft Skills and Working Style:</i></b></p><ul><li>
Capable of working independently with minimal supervision, taking initiative to identify and address challenges.</li><li>
Thrives in fast-paced environments with tight deadlines and evolving project priorities.</li><li>
Flexible and adaptable to last-minute changes in project scope or timelines.</li><li>
Strong problem-solving skills with a methodical approach to debugging and root cause analysis.</li><li>
Excellent communication and collaboration skills, able to convey complex technical concepts to diverse audiences.</li><li>
Passionate about innovation and continuous improvement, contributing creative ideas to improve validation processes.</li></ul></div><p></p>

Controls Software Validation Engineer

Hikma

<p></p><div><div><div><div><div><div><div>Description:
<p><b>Location: Saudi Arabia, Riyadh</b></p>
<p><b>
Job Type: [Full-time]</b></p>
<p><b>
Hashtag: #LI-NA1</b></p><br>
<p></p>
<p><b>
About Us:</b></p>
<p>
For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission.</p><br>
<p></p>
<p>
As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&amp;D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients.</p><br>
<p></p>
<p><b>
Description:</b></p><br>
<p></p>
<p>
We are looking for a talented <b>Validation Engineer </b>to join us. At Hikma you&rsquo;ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We&rsquo;re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together.</p><br>
<p></p>
<p>
If you want to be part of a team that cares about impact, this is the place for you.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<div>
<ul><li>Prepare all documents needed in validation (protocols, sampling plan, reports&hellip;etc.).</li></ul>
<ul><li>Reviewing, approving, and evaluating all documents generated in the validation department (SOPs, protocols, reports&hellip;etc.).</li></ul>
<ul><li>Monitor and execute the PV activities and collect the required samples.</li></ul>
<ul><li>Follow up on the approval of all PV documents.</li></ul>
<ul><li>Updating and reviewing process history.</li></ul>
<ul><li>Follow up plans and tasks on a daily basis.</li></ul>
<ul><li>Coordinating, planning, and advising with related departments for process activities.</li></ul>
<ul><li>Performing other duties related to the job as assigned by the direct supervisor/Manager.</li></ul>
<ul><li>Superb communication and interpersonal skills for coordinating between the various departments and staff of the company as well as the validation.</li></ul>
<ul><li>Knowledge of the various state and federal pharmaceutical validation laws and legislations that are enforced from time to time.</li></ul>
<ul><li>Must be well organized with good oral and written skills besides giving attention to details.</li></ul>
<ul><li>Verifying equipment, machines, instruments, and systems to be qualified.</li></ul>
<ul><li>Ensuring compliance with cGMPs for all related equipment, machines, instruments, and systems.</li></ul>
<ul><li>Calibration technician works with a variety of machinery, including analytic and electronic measuring devices.</li></ul></div><br>
<p></p>
<p><b>
Qualifications:</b></p>
<p>
We are looking for candidates whose experience and skills align closely with the qualifications outlined below:</p><br>
<p></p>
<p><b>
Education: </b>Bachelor's degree in engineering or pharmacist or relevant fields.</p>
<p><b>
Experience</b>: At least 0-3 years of experience in related fields</p>
<p><b>
Skills and Competencies:</b></p>
<ul>
<li>Good skill AutoCAD program is highly required</li>
<li>English fluency and reporting skills are highly required</li>
<li>Strong Numerical Skills</li>
<li>Analytical Thinking</li>
<li>Computer Skills</li>
<li>Initiative and Drive for Results</li>
<li>Collaboration and Teamwork</li>
<li>Change &amp; Innovation</li>
<li>Communication &amp; English fluency</li>
</ul>
<p><b>Learn more about Hikma in KSA </b><b>hikma-ksa-factsheet-aug-2025-en.pdf</b></p><br>
<p></p>
</div></div></div></div><div><div><div><div>Location:
Riyadh, SA, 11564</div></div></div></div></div></div></div><p></p>

Engineer, Validation

Julphar

<div></div><div><div><div><div><div><p>Detailed Job Description:</p>
<ul>
<li>Lead MS&amp;T activities supporting commercial manufacturing, technology transfer, and site readiness.</li>
<li>Act as the technical bridge between R&amp;D, Technology Transfer, Production, Quality, and Engineering.</li>
<li>Prepare, review, approve, archive, retrieve, and distribute validation documents.</li>
<li>Ensure compliance with GMP documentation and data integrity requirements.</li>
<li>Maintain validation master plans and validation schedules.</li>
<li>Ensure robust scientific understanding and control of manufacturing processes across the product lifecycle.</li>
<li>Support in writing the URS (user requirement specifications) for Project activities, ensuring all assets has URSs before entering the Purchasing Cycle</li>
<li>Follow-up with procurement and CAPEX manager</li>
<li>Support in preparation the technical evaluation of quotations from different vendors</li>
<li>Co-ordinate with procurement, MS&amp;T, QA in RAK site for any similar equipment procurement</li>
<li>Lead and execute the validation lifecycle using the V‑Model approach (URS, FAT, SAT, IQ, OQ, PQ, re‑qualification).</li>
<li>Ensure all critical utilities (PW, WFI, HVAC, compressed gases, nitrogen) remain in a validated state.</li>
<li>Ensure cleanroom qualification activities comply with ISO‑14644 requirements.</li>
<li>Review and approve validation protocols, reports, and risk assessments.</li>
<li>Lead or support investigations related to process deviations, OOS, OOT, and atypical results.</li>
<li>Perform root cause analysis using scientific and statistical tools.</li>
<li>Propose technically sound CAPAs and process improvements.</li>
<li>Support batch disposition decisions from a technical perspective.</li>
<li>Partner in FAT, SAT, DQ, IQ, OQ, PQ for equipment, CSV, systems (Water, utilities, HVAC, electricity, Thermal mapping).</li>
<li>Lead process validation activities for new and existing products.</li>
<li>Execute and oversee cleaning validation, sterilization validation, and transport validation.</li>
<li>Lead aseptic process simulation (media fills) and gowning qualification programs.</li>
<li>Support visual inspection qualification activities where applicable.</li></ul><br>
<p></p>
<p>
Core Competency:</p>
<ul>
<li>In terms of competency, you are highly result-oriented with an intense sense of accountability &amp; ownership.</li>
<li>High compliance adherence, having strong diligence, initiative-taking, and flexibility.</li>
<li>Excellent communication, interpersonal, and collaboration skills.</li>
<li>Must be able to manage tasks, plan workload effectively, prioritize, and easily adapt to changing situations.</li>
<li>Contribute to EHS activities, audits, and continual improvement initiatives.</li></ul><br>
<p></p>
<p>
Qualification/Functional Knowledge:</p>
<ul>
<li>Bachelor&rsquo;s degree in pharmacy, Chemical Engineering, Mechanical Engineering, Electrical Engineering, Industrial Engineering, or related scientific discipline<br>
(master&rsquo;s degree in pharmacy / engineering is an advantage)</li>
<li>Minimum 6&ndash;10 years of experience in pharmaceutical manufacturing within GMP‑regulated environments, with extensive hands‑on experience in qualification and validation activities</li>
<li>Strong and practical knowledge of:</li>
<li>cGMP, SFDA, WHO, EU GMP, and ICH guidelines</li>
<li>Qualification and validation lifecycle using the V‑Model approach</li>
<li>GMP documentation practices and regulatory inspection expectations</li>
<li>Proven experience in validation of:
<div><ul><li>Manufacturing equipment and production lines</li></ul>
<ul><li>Critical utilities (PW, WFI, HVAC, compressed gases, nitrogen)</li></ul>
<ul><li>Cleanrooms in compliance with ISO 14644</li></ul>
<ul><li>Sterile and non‑sterile manufacturing facilities</li></ul>
</div></li><li>Hands‑on experience in:
<div><ul><li>Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)</li></ul>
<ul><li>Re‑qualification and periodic review programs</li></ul>
<ul><li>FAT and SAT execution and documentation</li></ul>
</div></li><li>Strong experience in:
<div><ul><li>Process validation, cleaning validation, sterilization validation, and aseptic process simulation (media fills)</li></ul>
<ul><li>Gowning qualification, visual inspection qualification, and transport validation</li></ul>
</div></li><li>Practical knowledge of calibration systems, including rationale, acceptance criteria, frequency setting, and outsourced calibration management</li>
<li>Solid experience in Computerized System Validation (CSV):</li>
<li>Validation of manufacturing, utilities, QC, and validation systems</li>
<li>Compliance with 21 CFR Part 11 and data integrity (ALCOA+) principles</li>
<li>Strong experience in EQMS activities, including:</li>
<li>Change Control impact assessments</li>
<li>Deviation investigations and root cause analysis</li>
<li>CAPA development and effectiveness checks</li>
<li>Audit support and regulatory inspection readiness</li>
<li>Experience acting as validation SME during internal, customer, and regulatory audits, including SFDA inspections</li>
<li>Strong leadership and team‑coordination skills with experience assigning and reviewing work of validation engineers and SMEs</li>
<li>Excellent analytical, problem‑solving, and risk‑assessment skills</li>
<li>Proficiency in MS Office and electronic QMS / validation management system</li></ul></div></div></div></div></div><p></p>

Lead-MSAT (Validation)

Trinity Consultants - Advent Engineering

<div>
 <p>
  <strong>
   SUMMARY
  </strong>
 </p>
 <p>
  The CQV Engineer is responsible for the commissioning, qualification, and validation of facilities, utilities, process and laboratory equipment, and computerized systems to ensure compliance with cGMP regulations and internal quality standards. This role involves authoring and executing CQV protocols (IQ, OQ, PQ), coordinating with cross-functional teams, troubleshooting deviations, and preparing documentation in support of regulatory requirements. The position plays a key role in delivering compliant operational systems for manufacturing and laboratory environments.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   ESSENTIAL DUTIES AND RESPONSIBILITIES
  </strong>
 </p>
 <ul>
  <li>
   Develop, review, and execute Commissioning, Qualification, and Validation (CQV) protocols including DQ, FAT, SAT, IQ, OQ, and PQ for biopharmaceutical process, facilities/utilities systems and Process/laboratory equipment.
  </li>
  <li>
   Generate documentation such as C&amp;Q Plans and user requirement specifications (URS).
  </li>
  <li>
   Support start-up and commissioning activities for upstream, downstream bulk processing equipment (bioreactors/fermenters, chromatography skids, bioreactors, TFF, UFDF, centrifuge etc.), solid/ oral dosage equipment (tablet press, powder compactors, coating pans, compounding skids for mixing, etc.), critical utilities (WFI, process gases, pure steam, etc.), FFIP (formulation equipment, isolators, fillers, lyophilizer, etc.), and/or equipment used in Single Use application (e.g., SUBs, SUM, etc.)
  </li>
  <li>
   Perform equipment walkdowns, redline P&amp;IDs, and verify component installations.
  </li>
  <li>
   Participate in and/or lead risk assessments and design reviews (FAT, HAZOP, etc.).
  </li>
  <li>
   Coordinate with Quality Assurance, Engineering, Operations, and vendors to ensure timely execution of CQV deliverables.
  </li>
  <li>
   Identify and troubleshoot system discrepancies or failures during commissioning and qualification.
  </li>
  <li>
   Ensure adherence to project timelines and maintain clear communication across stakeholders.
  </li>
  <li>
   Generate and compile validation final reports, raw data, deviation records, and change controls.
  </li>
  <li>
   Support regulatory inspections by ensuring all validation documentation is complete and readily available.
  </li>
  <li>
   General working experience in Process Automation to support control narrative and sequences
  </li>
  <li>
   Familiarity in process instrumentation and components for hygienic application
  </li>
  <li>
   Familiarity with ASME BPE standards, ASTM E2500 risk-based C&amp;Q strategies, ISPE and USFDA regulatory requirements.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   SUPERVISORY RESPONSIBILITIES
  </strong>
 </p>
 <p>
  May directly supervise a number of technical/CQV team members during Commissioning and Qualification phase of the project.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   QUALIFICATIONS
  </strong>
 </p>
 <ul>
  <li>
   10+ years of experience in CQV or Validation within a regulated industry (pharmaceuticals, biotech, medical devices).
  </li>
  <li>
   Hands-on experience with commissioning and qualification of systems such as bioreactors, chromatography skids, CIP/SIP systems, HVAC, WFI, Clean Steam, autoclaves, etc.
  </li>
  <li>
   Proficiency with Good Documentation Practices (GDP), FDA regulations (21 CFR Part 11/210/211), ICH Q8-Q10, ISPE Baseline Guides (e.g., GAMP 5).
  </li>
  <li>
   Strong understanding of validation lifecycle and change control processes.
  </li>
  <li>
   Experience working with Delta V, PLC, SCADA, or other automation systems and PI Historian preferred.
  </li>
  <li>
   Excellent written and verbal communication skills.
  </li>
  <li>
   Strong analytical, organizational, and time-management skills.
  </li>
  <li>
   Strong troubleshooting skills to resolve issues and deviations observed during commissioning and qualification.
  </li>
  <li>
   Team-oriented but requires ability to work independently under limited supervision.
  </li>
  <li>
   Experience in consulting environment and engaging clients in projects that may have a dynamic schedule while multi-tasking other responsibilities is an asset.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   EDUCATION and/or EXPERIENCE
  </strong>
 </p>
 <p>
  Bachelor&rsquo;s degree (B.S.) in Engineering (Mechanical, Chemical, Electrical, Biomedical) or Life Sciences (Biology, Chemistry, Pharmacy) from four-year college or university or foreign equivalent.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Advanced degrees or certifications in validation, quality, or project management (e.g., ASQ, ISPE) are a plus.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Experience in consulting in Life Science industry and participate in delivering successful large-scale Engineering projects.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Must have computer literacy, including word processing, spreadsheet skills, and knowledge of Microsoft Office software package.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   LANGUAGE SKILLS
  </strong>
 </p>
 <p>
  Ability to clearly communicate technical concepts, write detailed protocols and reports, and interact effectively with cross-functional teams, vendors, and regulatory auditors.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Capable of drafting, reviewing, and revising high-quality validation documents, SOPs, and change controls in accordance with Good Documentation Practices (GDP).
 </p>
 <p>
  <br/>
 </p>
 <p>
  Able to convey complex ideas to both technical and non-technical stakeholders, including during meetings, training sessions, and inspections.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   MATHEMATICALSKILLS
  </strong>
 </p>
 <p>
  Strong analytical and problem-solving abilities are required to interpret engineering drawings, process data, and performance trends. Ability to interpret engineering documents such as drawings, piping lengths, welding requirements and modeling. Ability to perform engineering calculations related to flow rates, pressure drops, heat transfer, equipment sizing, and calibration tolerances to support commissioning and qualification activities.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   REASONING ABILITY
  </strong>
 </p>
 <p>
  Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   PHYSICAL DEMANDS
  </strong>
 </p>
 <p>
  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. The employee must also be able to travel onsite at a client&rsquo;s location to perform the job duties. The employee must be willing to travel to client/vendor sites if required (FAT/SAT support or multi-site projects).
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   WORK ENVIRONMENT
  </strong>
 </p>
 <p>
  The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The position will be primarily onsite at GMP manufacturing facilities, laboratories, or construction sites. May require off-shift or weekend work depending on project timelines and system availability.
 </p>
 <p>
  <br/>
 </p>
 <p>
  While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, outside weather conditions, risk of radiation, and vibration. The noise level in the work environment is usually moderate. Employee must be able to wear appropriate personal protective equipment (PPE) including gowning for cleanrooms.
 </p>
</div>


CQV Lead Engineer

ElMehy Engineering Company

<p><b>Pharmaceutical Calibration/Validation Manager Job </b></p><p><b>Job Description:</b></p><p>The Calibration &amp; Validation Engineer Manager is responsible for leading, managing, and continuously improving the organization&rsquo;s calibration and metrology activities ensuring full compliance with international standards (GMP, FDA, ISO/IEC 17025, and ISO 9001), regulatory requirements, and customer specifications. The position combines strong technical expertise, system development management and leadership role.</p><p><b>Key responsibilities:</b></p><p>&middot; Design &amp; implement the Calibration &amp; Validation department strategy, roadmap, procedure &amp; accreditation readiness, ensuring compliance with international standards and ongoing business needs.</p><p>&middot; Establish and maintain calibration policies, SOPs, workflow, work instructions and quality manuals.</p><p>&middot; Review &amp; approve calibration methods, validation protocols, results, certificates, and technical reports.</p><p>&middot; Ensure data integrity, traceability, and documentation compliance for all calibration and validation activities.</p><p>&middot; Specify, select, and procure calibration reference standards and calibration instruments.</p><p>&middot; Establish and manage equipment calibration, qualification, verification and re-calibration plans.</p><p>&middot; Optimize turnaround times and workflow efficiency for process improvement &amp; Operational Excellence.</p><p>&middot; Prepare, control and manage the calibration department budget.</p><p>&middot; Sourcing and selecting calibration engineers and technicians according to department needs plan.</p><p>&middot; Coach and mentor team members technically and professionally.</p><p>&middot; Define competency matrices, training programs, and authorization levels.</p><p>&middot; Build and sustain a culture of quality, accuracy, safety, and continuous improvement.</p><p>&middot; Drive continuous improvement initiatives and technical innovation.</p><p><b>Job Specifications:</b></p><p>&middot; Bachelor&rsquo;s degree in <b>engineering</b> (Electrical, Mechanical, Instrumentation, Mechatronics, or related field).</p><p>&middot; <b>10&ndash;15 years</b> of progressive experience in calibration, metrology and Validation.</p><p>&middot; <b>3&ndash;5 years&rsquo; </b>experience in a managerial position or leadership role.</p><p>&middot; Strong knowledge of: ISO/IEC 17025, ISO 9001, GMP, FDA</p><p>&middot; Previous experience in pharmaceutical, biotech, or regulated manufacturing environments is highly preferred.</p><p>&middot; Strategic thinker, strong managerial capability with experience in building systems, teams, and processes</p><p>&middot; Excellent decision-making and problem-solving skills</p><p>&middot; Strong communication and technical writing and documentation skills</p><p>&middot; High sense of ownership, accountability, and attention to details</p><p>Work Location: In person</p>

Calibration & Validation Manager

<div></div><div><div><div><div><ul><div>7 - 12 Years</div>
<div></div><div>1 Opening</div>
 <div>Bangalore, Chennai, Gurugram, Hyderabad, Kochi, Pune, Trivandrum</div></ul></div><p></p><div><br>
<div><div>
</div></div></div></div><div></div><div><h3 class="jobSectionHeader"><b>Role description</b></h3>
<div><p><b>Job Title:</b> Tableau QA Engineer</p>
<p><b>
Job Locations:</b> Bangalore / Hyderabad / Pune / Chennai / Trivandrum / Cochin / Gurugram</p>
<p><b>
Role Overview</b></p>
<p>
We are seeking a skilled <b>Tableau QA Engineer with Automation experience</b> to ensure the quality, accuracy, and performance of Tableau dashboards and enterprise reporting solutions. The role focuses on <b>data validation, dashboard testing, and test automation</b>, supporting large‑scale analytics programs. You will work closely with <b>BI Developers, Data Engineers, QA teams, and business stakeholders</b> in an Agile environment.</p>
<p><b>
Key Responsibilities</b></p>
<h3 class="jobSectionHeader"><b>
Tableau QA &amp; Data Validation</b></h3>
<ul><li>Perform end‑to‑end testing of <b>Tableau dashboards, reports, and data extracts</b></li>
<li>Validate data accuracy, completeness, and consistency between <b>source systems, data warehouses, and Tableau outputs</b></li>
<li>Test calculations, filters, parameters, aggregations, and drill‑downs</li>
<li>Identify data discrepancies, analyze root causes, and raise detailed defects with evidence</li>
</ul><h3 class="jobSectionHeader"><b>Test Automation</b></h3>
<ul><li>Design, develop, and maintain <b>automation test scripts</b> for Tableau dashboards and data validation</li>
<li>Automate <b>regression testing, data reconciliation, and dashboard validation</b></li>
<li>Integrate automation suites with <b>CI/CD pipelines</b> where applicable</li>
<li>Maintain reusable automation frameworks and test utilities</li>
</ul><h3 class="jobSectionHeader"><b>Functional &amp; Regression Testing</b></h3>
<ul><li>Execute <b>functional, regression, and smoke testing</b> for Tableau releases</li>
<li>Validate <b>dashboard performance, load behavior, and refresh schedules</b></li>
<li>Support <b>UAT cycles</b> in collaboration with business users and developers</li>
</ul><h3 class="jobSectionHeader"><b>Collaboration &amp; Reporting</b></h3>
<ul><li>Collaborate with <b>BI Developers, Data Engineers, QA, and Product teams</b></li>
<li>Participate in <b>sprint planning, reviews, and defect triage</b> meetings</li>
<li>Provide <b>test status, defect metrics, and quality reports</b> to stakeholders</li>
</ul>
<p><b>Required Skills &amp; Qualifications</b></p>
<ul>
<li>Hands on QA experience with a strong focus on <b>Tableau testing and data validation</b></li>
<li>Hands‑on experience with <b>Tableau Desktop, Tableau Server, and published dashboards</b></li>
<li>Strong <b>SQL</b> skills for backend data validation and reconciliation</li>
<li>Experience with <b>test automation tools/frameworks</b> (Selenium, Playwright, custom frameworks, or equivalent)</li>
<li>Good understanding of <b>data warehousing concepts and ETL/ELT pipelines</b></li>
<li>Experience working in <b>Agile / Scrum</b> delivery models</li>
</ul></div>
<h3 class="jobSectionHeader"><b>Skills</b></h3>
<div><p>Tableau, Test automation,data validation,selenium,data testing,playwright,restassured, BI Testing</p></div></div></div></div><p></p>
<br><div><h3 class="jobSectionHeader"><b>About UST</b></h3>
<div>UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world&rsquo;s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future-proof philosophy, UST embeds innovation and agility into their clients&rsquo; organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact&mdash;touching billions of lives in the process.</div></div>

Lead II - Software Testing (Tableau QA Engineer)

<div></div><div><div><div><div><ul><div>4 - 10 Years</div>
<div></div><div>1 Opening</div>
 <div>Bangalore, Chennai, Gurugram, Hyderabad, Kochi, Pune, Trivandrum</div></ul></div><p></p><div><br>
<div><div>
</div></div></div></div><div></div><div><h3 class="jobSectionHeader"><b>Role description</b></h3>
<div><p><b>Job Title: Tableau QA Engineer (Automation)</b></p>
<h3 class="jobSectionHeader"><b>
Experience: 4&ndash;10 Years</b></h3>
<h3 class="jobSectionHeader"><b>Location: </b><b>Bangalore/ Hyderabad/ Pune/ Chennai/ Trivandrum/ Cochin/ Gurugram</b></h3>
<p>Job Summary</p>
<p>
We are seeking a skilled <b>Tableau QA Engineer with Automation experience</b> to ensure the quality, accuracy, and performance of Tableau dashboards and reporting solutions.</p>
<p>
This role focuses on <b>data validation, dashboard testing, and test automation</b> to support enterprise analytics programs. The candidate will work closely with <b>BI Developers, Data Engineers, QA teams, and business stakeholders</b> in an Agile delivery environment.</p>
<p></p>
<p>Key Responsibilities</p>
<h3 class="jobSectionHeader"><b>
Tableau QA &amp; Data Validation</b></h3>
<ul><li>Perform end‑to‑end testing of Tableau dashboards, reports, and data extracts</li>
<li>Validate data accuracy, completeness, and consistency between source systems, data warehouses, and Tableau outputs</li>
<li>Test calculations, filters, parameters, aggregations, and drill‑downs for functional correctness</li>
<li>Identify data discrepancies, analyze root causes, and log clear defects with supporting evidence</li>
</ul><h3 class="jobSectionHeader"><b>Test Automation</b></h3>
<ul><li>Design, develop, and maintain automated test scripts for Tableau dashboards and data validation scenarios</li>
<li>Automate regression testing, data reconciliation, and dashboard validation checks</li>
<li>Integrate automation test suites with CI/CD pipelines for continuous quality validation (where applicable)</li>
<li>Maintain reusable automation frameworks, libraries, and utilities</li>
</ul><h3 class="jobSectionHeader"><b>Functional &amp; Regression Testing</b></h3>
<ul><li>Execute functional, regression, and smoke testing for Tableau releases</li>
<li>Validate dashboard performance, load behavior, and data refresh schedules</li>
<li>Support UAT cycles by coordinating closely with business users and development teams</li>
</ul><h3 class="jobSectionHeader"><b>Collaboration &amp; Reporting</b></h3>
<ul><li>Collaborate in Agile teams with BI Developers, Data Engineers, QA, and Product stakeholders</li>
<li>Participate in sprint planning, sprint reviews, and defect triage meetings</li>
<li>Provide regular test status updates, defect metrics, and quality reports to stakeholders</li>
</ul>
<p>Required Skills &amp; Qualifications</p>
<ul>
<li>4&ndash;10 years of QA experience with a strong focus on <b>Tableau testing and data validation</b></li>
<li>Hands‑on experience with <b>Tableau Desktop, Tableau Server, and published dashboards</b></li>
<li>Strong <b>SQL</b> skills for backend data validation and reconciliation</li>
<li>Experience with test automation tools/frameworks (Selenium, Playwright, custom frameworks, or equivalent)</li>
<li>Solid understanding of <b>data warehousing concepts, ETL/ELT pipelines, and BI reporting</b></li>
<li>Experience working in <b>Agile / Scrum</b> delivery models</li>
</ul>
<p>Preferred Qualifications</p>
<ul>
<li>Experience automating Tableau or BI validation using <b>Python or Java‑based frameworks</b></li>
<li>Exposure to cloud data platforms such as <b>AWS, Snowflake, Redshift, or Azure</b></li>
<li>Familiarity with <b>CI/CD tools</b> like Jenkins, Git, Azure DevOps</li>
<li>Experience working in <b>enterprise or regulated domains</b> (Healthcare, Insurance, BFSI)</li>
</ul></div>
<h3 class="jobSectionHeader"><b>Skills</b></h3>
<div><p>Tableau, Test automation, Data validation, Selenium, data testing, Python, Playwright, Restassured</p></div></div></div></div><p></p>
<br><div><h3 class="jobSectionHeader"><b>About UST</b></h3>
<div>UST is a global digital transformation solutions provider. For more than 20 years, UST has worked side by side with the world&rsquo;s best companies to make a real impact through transformation. Powered by technology, inspired by people and led by purpose, UST partners with their clients from design to operation. With deep domain expertise and a future-proof philosophy, UST embeds innovation and agility into their clients&rsquo; organizations. With over 30,000 employees in 30 countries, UST builds for boundless impact&mdash;touching billions of lives in the process.</div></div>

Lead II - Software Testing (Tableau QA Engineer (Automation))

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