What Jobs are available for Software Testing in Delhi?

• Design, develop, and implement QA strategies and test plans for automotive products.
• Conduct thorough inspections and testing of components, sub-assemblies, and finished vehicles.
• Analyze test data and product quality metrics to identify trends and areas for improvement.
• Collaborate with design and manufacturing engineers to address quality concerns and implement corrective actions.
• Ensure compliance with industry standards (e.g., IATF 16949, ISO 9001) and customer-specific requirements.
• Develop and maintain detailed quality documentation, including test reports and failure analysis.
• Perform root cause analysis for quality defects and implement preventive measures.
• Lead quality improvement initiatives and continuous improvement activities.
• Train and mentor junior QA personnel on quality standards and testing procedures.
• Manage supplier quality performance and conduct supplier audits.
• Stay updated on emerging quality trends and technologies in the automotive sector.
• Contribute to the continuous improvement of the company's quality management system.

About Us

GVR Technolabs Pvt Ltd , an Information Technology services company with expertise in design, deployment and management of hardware and software applications and technology infrastructures. We offer services to improve our clients efficiency, strengthen partnerships, increase profitability, and improve business processes with quality and value in a secure environment.

Designation: Software Quality Assurance (IV & V Services)

Locations: Delhi

Qualification: B.Tech/BE/M.Tech/ME in ECE/CSE/EEE/ECE/E & TCE or MSc (CS) or MCA

Experience Required

   2 Years for Regular level

   4 Years for High level

Roles & Responsibilities:

• Checklists tailoring and compliance verification for specific Lab/Estt. needs
• Analysis of software code, design and related artifacts (code, documents, scripts) and preparation of reports
• High level requirements to low level requirements to design to implementation to test cases traceability and report generation
• Execution of test vectors, generation of test oracles / data set
• Test coverage based on test execution plan and report generation
• Execution of functional, non-functional and endurance tests w.r.t ATP document
• First level identification, reporting verification on closure of defects & bug
• Review of documentation for completeness, consistency, traceability and reporting
• Test measurements reports generation and analysis
• Static and dynamic testing reports generation and review
• Development of automated regression test suites and regression testing based as per test plans.
• Test report generation for certification, where applicable
• Preparation of required documentation for the air-worthiness certification or equivalent certifications for all levels of criticality
• Generation of result reports for the IV&V activities carried out
• Use of configuration tools for software configuration control
• Configuration audits and report generation
• Software quality metrics data recording and analysis, and reporting
• Review of requirements, design, interfaces/ protocols and documents and release the review reports/ audit reports
• Verification/ updating of low level test plan, test cases and test procedures (Unit testing and module testing)
• Integration testing and analysis and report generation
• Requirements based testing &test case generation w.r.t functional requirements
• Generation of endurance test cases and realization of endurance test beds.
• Generation of smoke &sanity tests results, review and validation of the same
• Reverification of identification and reporting on closure of defects & bugs
• Verification of test beds/prototypes similar to deliverable system
• Development of test procedure and test scripts for HSI testing based on requirements
• Execution & reporting and review of HSI testing
• Phase checks, Integration testing and analysis of final V&V reports
• End to end traceability review
• Generation and verification of functional and non-functional requirement test cases.
• Code walkthrough and review and reporting
• Object code testing and review and reporting
• FPGA/ Verilog/ VHDL code review and reporting
• Third party library testing and report generation
• Verification of software tool qualification and documentation
• Impact analysis and change request-based testing and regression analysis
• Mutation testing with debugging, fault injection at unit, component & system level
• Defect identification and tracking
• Preparation and management of trace data
• Development/ updation of software IV&V plan as per the standard/ guidelines
• Testing using jigs, simulators and test beds
• Define IV&V processes and methodologies
• Review and validation of all test plans, suites and results including automated regression test suites
• Analysis of software quality metrics data as per established process and product metrics
• Audit of all reviews
• Audit of all IV&V processes
• Validation of deliverable systems w.r.t functional and non-functional requirements
• Behavioral testing and reliability assessment
• Generation/ validation of FAT and ATP documents
• Review of all documents related to qualification and certification and release the same

Requirements

• Flight control software (S/W residing on on-board computers of launch vehicles) and on-board mission systems and avionics
• Ground based software (S/W residing in checkout systems and simulation test facilities of launch vehicles)
• Ground based armament and combat systems
• Verification simulators software and Test rig software
• Mission planning, design and training Software
• Engine control software
• Radar and Communication software Signal processing & analysis software
• Shipborne/ Under water systems software
• Simulation & Modeling software
• Other software required to build mission critical / safety critical systems
• Other general-purpose software in Aerospace and Defence domain.
• Other software application using web technologies and RDBMS

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with global regulatory requirements.
• Oversee all quality assurance activities, including batch record review, product release, and deviation management.
• Conduct regular internal audits of manufacturing processes, laboratories, and documentation to ensure compliance.
• Manage external audits from regulatory authorities and customers, coordinating responses and follow-up actions.
• Investigate product quality complaints, deviations, and out-of-specification (OOS) results, implementing robust CAPA plans.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards.
• Develop and deliver quality training programs for relevant personnel.
• Review and approve validation protocols and reports for equipment, processes, and analytical methods.
• Manage supplier quality, including qualification, auditing, and performance monitoring.
• Lead continuous improvement initiatives aimed at enhancing product quality, process efficiency, and regulatory compliance.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry.
• Extensive knowledge of GMP, regulatory guidelines (e.g., FDA, EMA), and quality systems.
• Proven experience in conducting and managing audits (internal and external).
• Strong understanding of pharmaceutical manufacturing processes, validation, and stability studies.
• Excellent analytical, problem-solving, and decision-making skills.
• Effective leadership and team management abilities.
• Strong written and verbal communication skills, with the ability to present complex information clearly.
• Proficiency in using quality management software and ERP systems.
• Ability to work effectively in a regulated manufacturing environment.

• Oversee and manage the Quality Management System (QMS) for pharmaceutical products.
• Ensure compliance with GMP, GLP, and other relevant regulatory standards.
• Lead the review and approval of batch records, specifications, and validation protocols.
• Manage deviation investigations, root cause analysis, and CAPA implementation.
• Conduct internal audits and support external regulatory inspections.
• Develop and implement quality training programs for personnel.
• Monitor and analyze quality metrics to drive continuous improvement.
• Collaborate with R&D, manufacturing, and regulatory affairs departments.
• Approve or reject raw materials, intermediates, and finished products.
• Stay abreast of evolving pharmaceutical regulations and quality best practices.

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with global regulations.
• Oversee and manage all QA activities, including batch record review, release, deviation investigations, CAPA, and change control.
• Lead internal audits and host regulatory agency inspections (e.g., FDA, EMA) and customer audits.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant industry standards.
• Develop and execute validation master plans and protocols for equipment, processes, and systems.
• Review and approve product quality related documentation, ensuring accuracy and completeness.
• Manage and mentor a team of Quality Assurance professionals, fostering their development and performance.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs to ensure quality is built into products and processes.
• Drive continuous improvement initiatives within the QA function to enhance efficiency and compliance.
• Stay updated on evolving regulatory requirements and industry best practices.

• Master's degree or Ph.D. in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related life science field.
• Minimum of 8-10 years of progressive experience in Quality Assurance within the pharmaceutical industry.
• Extensive knowledge of GMP, ICH guidelines, and global regulatory requirements.
• Proven experience in managing QMS, conducting audits, and leading regulatory inspections.
• Strong leadership, team management, and interpersonal skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Exceptional written and verbal communication skills.
• Ability to work independently and effectively in a fully remote environment.

• Develop, implement, and manage the company's Quality Management System (QMS) in compliance with global pharmaceutical regulations (e.g., FDA, EMA, WHO).
• Oversee and ensure adherence to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Clinical Practices (GCP).
• Lead and mentor the Quality Assurance team, fostering a culture of quality and continuous improvement.
• Conduct internal audits and support external regulatory inspections and audits from health authorities.
• Review and approve batch records, validation protocols, and reports.
• Manage deviations, investigations (CAPA), change controls, and risk assessments.
• Ensure that all pharmaceutical products meet established quality standards and specifications.
• Collaborate with R&D, Manufacturing, Regulatory Affairs, and other departments to resolve quality issues and drive product quality improvements.
• Stay updated on evolving regulatory requirements and industry best practices.
• Develop and deliver quality training programs to relevant personnel.
• Manage vendor qualification and ongoing supplier quality agreements.
• Prepare and present quality metrics and reports to senior management.

• Master's or Ph.D. in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 10-15 years of progressive experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
• Deep understanding of pharmaceutical manufacturing processes, quality control, and regulatory compliance.
• Proven experience in managing QMS, conducting audits, and successfully navigating regulatory inspections.
• Strong knowledge of GMP, ICH guidelines, and other relevant international regulatory standards.
• Excellent leadership, team management, and interpersonal skills.
• Exceptional analytical, problem-solving, and decision-making abilities.
• Superior written and verbal communication skills, with the ability to present complex information clearly.
• Proficiency in using quality management software and tools.
• Ability to work independently and effectively manage multiple priorities in a remote setting.
• Commitment to upholding the highest ethical and quality standards.

• Develop and implement comprehensive quality assurance plans for automotive products.
• Define quality standards, metrics, and key performance indicators (KPIs).
• Establish and oversee testing procedures for components, systems, and finished vehicles.
• Analyze quality data, identify trends, and conduct root cause analysis for defects.
• Implement and manage Corrective and Preventive Actions (CAPA) processes.
• Ensure compliance with automotive quality standards (e.g., IATF 16949).
• Collaborate with engineering, manufacturing, and supply chain teams to resolve quality issues.
• Conduct supplier quality audits and manage supplier performance.
• Lead cross-functional teams in quality improvement initiatives.
• Prepare quality reports and present findings to management.

• Bachelor's degree in Engineering (Mechanical, Electrical, or relevant field).
• Minimum of 6 years of experience in Quality Assurance within the automotive industry.
• Strong knowledge of automotive quality standards and methodologies (IATF 16949, APQP, PPAP, FMEA).
• Proficiency in statistical analysis tools and techniques (SPC).
• Experience with various testing methods and equipment.
• Excellent problem-solving, analytical, and critical thinking skills.
• Strong communication, interpersonal, and leadership abilities.
• Ability to work effectively in a cross-functional team environment.