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Head of Quality Assurance

Delhi, Delhi Progressive Steel Automotive Solution Pvt Ltd

Posted 1 day ago

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Job Description

Company Description


Progressive Steel Automotive Solution Pvt Ltd, a prominent Motorcycle sprocket manufacturer in India, was established in 1997. The company has evolved into a leading Sprocket manufacturer in India. Over the years, we have embraced technological advancements and consistently met customer demands with innovative solutions. Today, we take pride in being the foremost producer of Motorcycle Sprockets under the renowned brand ‘Progressive’. With three manufacturing facilities and several warehouses, all adhering to ISO 9001:2015 and IATF 16949 standards, we have a collective capacity of producing 6 million Sprockets.


Role Description


This is a full-time on-site role for a Head of Quality Management located in Delhi, India. The Head of Quality Management will be responsible for overseeing all aspects of quality assurance and control across the organization. This includes developing and implementing quality management systems, conducting quality audits, managing quality control processes, and ensuring compliance with industry standards and regulations. The role also involves analyzing data to identify areas for improvement and training staff on quality best practices.


Qualifications


  • Proficiency in Quality Control and Quality Assurance
  • Experience with Quality Auditing and Quality Management systems
  • Strong Analytical Skills
  • Excellent leadership and communication skills
  • Ability to work collaboratively with cross-functional teams
  • Minimum of 7-10 years experience in a quality management role
  • Bachelor's degree in Engineering, Quality Management, or related field; advanced degree preferred
  • Audit knowledge of IATF 16949, ISO 9001 and related certifications
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Senior Quality Assurance Manager

Delhi, Delhi PharmaSecure

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Job Description

Job Title: Sr. Manager - Quality

Location: Delhi, India

Status: Full-Time


About PharmaSecure

PharmaSecure is a global track-and-trace, product authentication, and consumer engagement company that has helped protect over 8 billion packages through its technology-enabled solutions on hundreds of manufacturing lines. The codes printed are generated using its patented, encryption-based algorithm that provides unmatched security.


It has a proven track record of implementing minimal changes to the existing manufacturing process and negligible downtime of manufacturing lines by providing a solution that seamlessly integrates into the existing operations.


It’s proven serialization capabilities have enabled large pharmaceutical companies to meet different traceability requirements, as it ensures that pharma manufacturers exporting to various countries maintain regulatory compliances.


Other than being experts in global track-and-trace, product authentication, and consumer engagement, PharmaSecure is also an OEM for efficient machines to provide a full suite of software and hardware solutions under one umbrella.


Overview of Role

The Senior Manager – Quality will be responsible for ensuring the quality and compliance of software applications, IT systems, and related processes in alignment with regulatory requirements in the pharmaceutical sector. The role involves testing, validating, and verifying that all systems meet industry standards, including GxP compliance, 21 CFR Part 11, and other applicable regulations. The candidate should have a keen eye for detail, a strong understanding of pharma industry guidelines, and experience in software testing and validation.


Principal Responsibilities and Accountabilities

  • Software Testing & Validation :
  • Design and/or review manual and automated test cases for IT systems.
  • Perform validation of pharma-related IT systems as per GMP guidelines.
  • Ensure compliance with 21 CFR Part 11 and other global pharmaceutical regulatory standards.
  • Ensure testing for all IT systems and applications is in-line with PhrmaSecure QMS.
  • Supervise Manage defect tracking and resolution with development teams.
  • Documentation :
  • Prepare/Review validation documentation, including Test Plans, Test Scripts, Validation Protocols, and Reports (IQ/OQ/PQ).
  • Maintain records of test results, issues identified, and corrective actions.
  • Assist in maintaining Standard Operating Procedures (SOPs) and ensuring they are followed during testing and validation activities.
  • Regulatory Compliance :
  • Ensure IT systems and processes adhere to industry-specific regulatory standards (GxP, GMP, GAMP 5, and Data Integrity requirements) and maintain continuous compliance.
  • Oversee both QA and Regulatory Affairs responsibilities to ensure alignment with evolving pharmaceutical and IT regulations.
  • Act as the primary liaison for internal and external audits, ensuring all IT systems meet regulatory and compliance standards.
  • Stay updated on regulatory changes affecting pharma IT systems and incorporate new requirements into QA and regulatory processes.
  • Risk Management :
  • Conduct risk assessments and develop mitigation strategies for IT systems.
  • Identify potential risks and issues early in the development lifecycle to prevent system failures post-deployment.
  • Collaboration & Support :
  • Work closely with cross-functional teams (IT, Development, Manufacturing, Regulatory, etc.) to ensure a smooth transition of systems from development to production.
  • Provide training and support to end-users for validated IT systems.
  • Assist with internal and external audits, ensuring IT QA compliance is maintained.

Competencies

  • Fluency in English.
  • Excellent written and verbal communication skills.
  • Excellent teamwork skills.
  • Excellent attention to detail, quality and control.
  • Proven ability to influence cross-functional teams without formal authority.



Required experience and knowledge

  • 10 plus years of experience in IT Quality Assurance, preferably in the pharmaceutical or life sciences sector.
  • Proven track record of validating GxP-compliant systems in a regulated environment.
  • Familiarity with GAMP 5, 21 CFR Part 11, Data Integrity, and other relevant pharma regulations.
  • Bachelor's or Master's degree in Information Technology, Computer Science, or a related field.
  • Certifications like ISTQB, Six Sigma, or relevant QA certifications are a plus.
  • Hands-on experience with test management tools (JIRA, HP ALM, etc.).
  • Knowledge of SQL and scripting for database and application testing.
  • Familiarity with automated testing tools (Selenium, QTP, etc.).
  • Experience with ISO standards 9001 and 27001.
  • Knowledge of Pharma machines validation will be an added advantage.


Compensation

Candidates that meet all the above requirements will be considered for competitive compensation commensurate with their experience.

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Quality Assurance Manager - Manufacturing

110001 Delhi, Delhi ₹1300000 Annually WhatJobs Direct

Posted 2 days ago

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Job Description

full-time
Our client is a leading manufacturing firm seeking a highly experienced and detail-oriented Quality Assurance Manager to oversee and enhance their quality management systems. This crucial role involves ensuring that all manufactured products meet stringent quality standards, regulatory requirements, and customer expectations. The ideal candidate will possess a deep understanding of quality control methodologies, statistical process control (SPC), and a proven ability to lead and mentor quality assurance teams.

Responsibilities:
  • Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with relevant standards (e.g., ISO 9001, industry-specific certifications).
  • Establish and monitor key quality metrics and performance indicators, implementing corrective and preventive actions (CAPA) as needed.
  • Lead and manage the Quality Assurance team, providing guidance, training, and performance evaluations.
  • Oversee all aspects of product quality, from raw material inspection to finished goods testing and release.
  • Conduct internal audits and support external audits by regulatory bodies and customers.
  • Collaborate with production, engineering, and R&D teams to identify and resolve quality issues promptly.
  • Implement and manage statistical process control (SPC) techniques to monitor and control manufacturing processes.
  • Develop and update quality control procedures, work instructions, and documentation.
  • Investigate customer complaints related to product quality and implement effective solutions.
  • Drive continuous improvement initiatives to enhance product quality, reduce defects, and optimize manufacturing processes.
  • Manage supplier quality assurance programs, including audits and performance monitoring.
  • Ensure compliance with all applicable health, safety, and environmental regulations related to quality.
  • Prepare regular reports on quality performance for senior management.
  • Promote a strong quality culture throughout the organization.
  • Stay current with evolving quality standards and best practices in the manufacturing industry.

The ideal candidate will hold a Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a relevant scientific discipline, with a minimum of 6 years of experience in Quality Assurance within a manufacturing environment. Experience with ISO 9001 certification and implementation is essential. Strong knowledge of quality control tools, statistical analysis, SPC, and problem-solving methodologies (e.g., Six Sigma, Lean Manufacturing) is required. Excellent leadership, communication, and interpersonal skills are critical for managing the QA team and collaborating effectively with other departments. Proficiency in quality management software and standard office applications is expected. This role is based in **Delhi, Delhi, IN** and operates on a hybrid model, requiring a balance of in-office presence for team leadership and process oversight, with flexibility for remote work.

We are seeking a dedicated and proactive leader committed to upholding the highest quality standards and driving manufacturing excellence. If you are passionate about quality and ready to make a significant impact in a leading manufacturing organization, we encourage you to apply.
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Automotive Quality Assurance Engineer

110001 Delhi, Delhi ₹60000 Annually WhatJobs

Posted 16 days ago

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Job Description

full-time
Join WhatJobs as an Automotive Quality Assurance Engineer , a critical role focused on ensuring the highest standards of quality in automotive components and systems. This position is based in Delhi, Delhi, IN and offers a hybrid work model, blending the benefits of in-office collaboration with remote flexibility. The ideal candidate will have a robust understanding of automotive manufacturing processes, quality control methodologies, and regulatory compliance. You will be responsible for developing and implementing comprehensive quality assurance plans, conducting rigorous testing, and collaborating with engineering and production teams to resolve quality issues.

Key Responsibilities:
  • 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.

This role demands meticulous attention to detail, strong analytical skills, and excellent communication abilities. You should be proficient in using various quality control tools and techniques. A passion for the automotive industry and a commitment to delivering defect-free products are essential. The successful candidate will be a team player, capable of working effectively across different departments. We are looking for an individual who can take ownership of quality initiatives and drive positive change. If you are ready to make a significant impact in the automotive quality domain, we encourage you to apply for this exciting opportunity in Delhi, Delhi, IN .
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Quality Assurance Automation Engineer

Delhi, Delhi GVR TECHNOLABS PRIVATE LIMITED

Posted 27 days ago

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Job Description

full-time

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
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Senior Pharmaceutical Quality Assurance Manager

110001 Delhi, Delhi ₹1800000 Annually WhatJobs Direct

Posted today

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Job Description

full-time
Our client, a prominent pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to lead their QA operations. This is a critical, fully remote position, offering the opportunity to shape quality standards and compliance initiatives from anywhere. You will be responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS) in accordance with global regulatory requirements, including GMP, ICH guidelines, and relevant health authority regulations. Your role will involve overseeing all aspects of QA, including batch record review, deviation management, CAPA implementation, change control, internal and external audits, and validation activities. You will play a pivotal role in ensuring product quality and patient safety throughout the drug development and manufacturing lifecycle. The ideal candidate possesses a deep understanding of pharmaceutical manufacturing processes, regulatory affairs, and quality control principles. Strong leadership skills, exceptional analytical and problem-solving abilities, and excellent communication and interpersonal skills are essential for effectively managing QA teams and collaborating with cross-functional departments such as R&D, Manufacturing, and Regulatory Affairs. As a remote leader, you must be highly organized, self-motivated, and adept at utilizing virtual collaboration tools to maintain effective communication and workflow with teams potentially working near **Delhi, Delhi, IN** and globally. You will also be responsible for driving continuous improvement initiatives within the QA function, mentoring QA personnel, and ensuring a culture of quality excellence throughout the organization. This position demands a proactive and detail-oriented professional committed to upholding the highest standards of pharmaceutical quality.

Responsibilities:
  • 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.
Qualifications:
  • 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.
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Senior Pharmaceutical Quality Assurance Manager

110001 Delhi, Delhi ₹130000 Annually WhatJobs Direct

Posted 2 days ago

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Job Description

full-time
Our client is seeking a highly experienced Senior Pharmaceutical Quality Assurance Manager to oversee and enhance quality systems at their facility in **Delhi, Delhi, IN**. This critical role ensures compliance with all relevant regulatory standards, including GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and GDP (Good Distribution Practices). You will be responsible for developing, implementing, and maintaining robust quality assurance programs, leading internal and external audits, and managing deviations and corrective/preventive actions (CAPAs). The ideal candidate will possess an in-depth understanding of the pharmaceutical manufacturing process, quality control methodologies, and regulatory requirements. You will lead and mentor a team of QA professionals, fostering a culture of quality excellence and continuous improvement. Key responsibilities include reviewing and approving batch records, validation protocols, and change controls; investigating quality incidents; and ensuring the integrity and reliability of all manufactured products. Strong leadership, analytical, and problem-solving skills are essential. The ability to communicate effectively with regulatory agencies, senior management, and cross-functional teams is paramount. A Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, along with a minimum of 8 years of progressive experience in pharmaceutical quality assurance, is required. Experience in managing QA teams and conducting regulatory inspections is highly desirable. Familiarity with Quality Management Systems (QMS) and relevant software applications is also expected. This is an exceptional opportunity to take on a leadership role in ensuring the highest standards of quality and compliance within the pharmaceutical industry, contributing significantly to patient safety and product efficacy.
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Lead Quality Assurance Engineer - Automotive

110001 Delhi, Delhi ₹130000 Monthly WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a pioneering automotive technology company revolutionizing the industry, is seeking a highly motivated and experienced Lead Quality Assurance Engineer to spearhead their quality control efforts. This is a fully remote position, offering the opportunity to work from anywhere within India, contributing to the development of next-generation automotive systems. The ideal candidate will possess a deep understanding of automotive engineering principles, quality management systems, and advanced testing methodologies. You will be responsible for defining and implementing robust quality assurance strategies, leading a team of QA professionals, and ensuring that all products meet the highest standards of performance, reliability, and safety.

Key responsibilities include developing comprehensive test plans, test cases, and test scripts for automotive software and hardware components. You will oversee the execution of various testing phases, including unit testing, integration testing, system testing, and performance testing. This involves identifying, documenting, and tracking defects through to resolution. The successful candidate will work closely with development teams to ensure seamless integration of quality assurance processes throughout the product development lifecycle. Experience with embedded systems, automotive communication protocols (e.g., CAN, LIN), and functional safety standards (e.g., ISO 26262) is highly desirable. You will also be responsible for establishing and maintaining quality metrics, analyzing test results, and providing regular reports to senior management.

The role demands strong leadership capabilities, excellent analytical and problem-solving skills, and the ability to mentor and guide junior QA engineers. You will be expected to champion a culture of quality throughout the organization. Proficiency in test automation tools and scripting languages (e.g., Python, C++) is essential. Experience with Agile/Scrum methodologies and defect tracking tools (e.g., Jira) is required. The ability to communicate effectively with cross-functional teams, including hardware engineers, software developers, and product managers, is crucial. This is an exceptional opportunity to shape the quality assurance framework for groundbreaking automotive technologies and drive innovation from a remote setting, impacting the future of mobility in Delhi, Delhi, IN .
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Senior Pharmaceutical Quality Assurance Manager

110001 Delhi, Delhi ₹1800000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a highly qualified Senior Pharmaceutical Quality Assurance Manager to lead their quality operations. This is a crucial, fully remote position, allowing you to oversee quality systems and ensure compliance from anywhere within India. The ideal candidate will possess extensive experience in pharmaceutical quality assurance, GMP (Good Manufacturing Practices), regulatory affairs, and quality control. You will be responsible for developing, implementing, and maintaining robust quality management systems to ensure product safety, efficacy, and regulatory compliance across all stages of drug development and manufacturing. This role demands a strategic thinker with exceptional leadership and analytical skills.

Key Responsibilities:
  • 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.

Qualifications:
  • 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.

This is a senior leadership opportunity within a highly respected pharmaceutical organization, offering significant impact and career advancement in a fully remote capacity. If you are a dedicated Quality Assurance professional ready to lead and innovate, we encourage you to apply.
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Senior Automotive Quality Assurance Engineer

110011 Delhi, Delhi ₹70000 Monthly WhatJobs

Posted 9 days ago

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full-time
Our client, a leading automotive manufacturer, is seeking a highly motivated and detail-oriented Senior Automotive Quality Assurance Engineer to join their team in Delhi, Delhi . This role is critical in ensuring the highest standards of quality throughout the vehicle development and production lifecycle. You will be responsible for developing and implementing robust quality assurance strategies, methodologies, and processes to meet and exceed industry standards and customer expectations. Your duties will include defining quality metrics, establishing testing protocols, analyzing quality data, and identifying root causes of defects. You will collaborate closely with design, engineering, manufacturing, and supplier teams to proactively address quality issues and implement corrective and preventive actions (CAPA). Experience with quality management systems (e.g., IATF 16949), statistical process control (SPC), and various testing methodologies (e.g., functional, performance, reliability) is essential. The ideal candidate will possess strong analytical and problem-solving skills, a meticulous approach to quality control, and excellent communication abilities to effectively interface with diverse teams. This hybrid role requires on-site presence for critical quality inspections and team collaborations, with flexibility for remote strategic planning and data analysis.

Responsibilities:
  • 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.
Qualifications:
  • 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.
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