169 Validation Testing Jobs

Automotive Software Validation Engineer Location-Hyderabad Salary- 20LPA Profile 1 – Kotlin / Java Validation -software validation using Kotlin & Java. Profile 2 – C++ Validation -software validation using C++ -automotive domain Resume @ 7290012570

Role & responsibilities Conduct functional, performance, stability, and reliability testing of IVD instruments. Develop and standardize QC protocols for hardware, firmware, and system-level performance. Validate calibration, precision, and repeatability of instrument test results. Perform environmental and stress testing to ensure robustness of instruments. Support product development by testing prototypes and providing QC data to R&D. Investigate instrument malfunctions during QC and provide feedback for improvements. Collaborate with service teams to analyze field performance and incorporate learnings into QC processes. Maintain QC test logs, calibration records, and instrument performance data. Responsibilities Reagents Conduct chemical, biochemical, and functional testing of reagent batches. Ensure lot-to-lot consistency, stability, and accuracy of reagents. Develop and optimize QC test methods specific to reagent performance with instruments. Perform precision, sensitivity, and linearity testing of reagents. Maintain control samples and reference standards for reagent QC. Support troubleshooting of reagent-related issues in coordination with production and service teams. Document reagent QC results and prepare stability and shelf-life reports. Team Management & Leadership Lead, train, and mentor the QC team to ensure adherence to test protocols and accuracy. Allocate resources, assign tasks, and monitor team performance for timely QC operations. Conduct regular training on instruments, reagents, and testing procedures. Drive continuous improvement initiatives within the QC department. Ensure proper maintenance and availability of QC equipment and consumables Preferred candidate profile M.Sc. or B.Sc. in Biochemistry or Chemistry (mandatory). 10 12 years of experience in Quality Control, with at least 3–5 years in a leadership role. Strong knowledge of QC testing methods for IVD instruments and reagents. Hands-on experience with calibration, stability studies, and performance validation. Excellent troubleshooting and analytical skills. Proven ability to lead a QC team and manage multiple priorities. Strong documentation, reporting, and data interpretation skills.

Key Role 1. Develop, write, and maintain compliance and quality-related documents, including: 2. Standard Operating Procedures (SOPs) 3. Work Instructions (WIs) 4. Validation Protocols (IQ/OQ/PQ) 5. Risk Assessments 6. Quality Manuals 7. Audit Response Documentation 8. Collaborate with QA, Regulatory, IT, and Project teams to gather inputs and ensure document accuracy and clarity. 9. Translate complex technical and regulatory content into structured, user-friendly documentation. 10. Ensure all content complies with applicable FDA , EMA , and ICH guidelines and client-specific quality frameworks. 11. Assist in preparing documentation for client audits, internal assessments, and regulatory inspections. 12. Maintain version control, change history, and document archiving using tools like SharePoint , Veeva Vault , or Documentum . Contribute to the development of training materials and knowledge-sharing resources Role & responsibilities Technology Hands on Exp : AWS, Azure, GCP, SAS, BI, Databricks, sFTP, SaaS, PaaS, IaaS Domain: GDP, GxP, GAMP, CRO, 21 CFR Part 11, FDA, NDA, ALCOA+, QMS, SOP Preferred candidate profile We are striclty looking for System Validation side not For Medical Devices, Equipments or Instruments validation side Relevant Work Experience/Job Requirements: 1. Hands-on experience in Computer System Validation (CSV) including preparation of VMP, URS, FS, RTM, IQ/OQ/PQ, and validation reports . 2. Strong understanding of GxP, 21 CFR Part 11, EU Annex 11, and GAMP 5 guidelines with exposure to regulatory audits . 3. Experience with quality and compliance documentation including SOPs, change controls, deviations, and CAPA in a pharma environment. 4. Practical knowledge of EDMS/QMS systems, LIMS, MES, and electronic signature platforms . 5. Proven ability to collaborate with QA, IT, Manufacturing, and Regulatory teams for compliant system implementation and maintenance. Must have Skill sets required: 1. Computer System Validation (CSV) Expertise Hands-on in preparing and executing VMP, URS, FS, RTM, IQ/OQ/PQ, and validation reports. 2. Regulatory & Compliance Knowledge Strong understanding of GxP, 21 CFR Part 11, EU Annex 11, GAMP 5, and data integrity principles. 3. Quality Documentation & Audit Readiness Skilled in SOPs, change control, CAPA, deviations, and maintaining audit-ready records. 4. Technical & System Knowledge Familiar with EDMS, QMS, LIMS, MES, and electronic signature platforms in regulated environments. 5. Cross-functional Collaboration & Communication Ability to work closely with QA, IT, Manufacturing, and Regulatory Affairs teams. Technology Hands on Exp : AWS, Azure, GCP, SAS, BI, Databricks, sFTP, SaaS, PaaS, IaaS Domain: GDP, GxP, GAMP, CRO, 21 CFR Part 11, FDA, NDA, ALCOA+, QMS, SOP Other Skills: 1. Risk Assessment & Impact Analysis Ability to perform risk-based validation and assess system changes for regulatory impact. 2. Data Integrity & Audit Trail Review – Ensuring compliance with ALCOA+ principles and monitoring system audit trails.

Develop, implement, and maintain Quality Assurance systems , final inspections , . Work closely with production, design, and supply chain Lead root cause analysis (RCA) and corrective/preventive actions (CAPA) , . Review and interpret.

SUMMARY OF THE OVERALL JOB To be responsible for implementing and managing the Quality Management System To ensure the compliance of Quality in R & D and to approve all the technical documents. To be also responsible for Quality oversight through Quality Plan . Stay abreast with GMP requirements and on time training within the team as well as cross functional teams. KRA Management of state of control for QMS elements through Quality oversight. Effective implementation, monitoring and maintenance of the QMS. On time availability of approved specification and STP to QC. To ensure ISO certification audits are performed on time successfully and ensure compliance. Ensuring timely approval and closure of QMS documents Provide training to all departments on GMP topics. Procedural requirements Prepare the Opex and Capex budget Ensuring conforms to the requirement of ISO standards. Ensuring Ops Excellence To ensure implementation of strategic decisions related to Quality

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Job Requirements At Quest Global, it’s not just what we do but how and why we do it that makes us different. With over 25 years as an engineering services provider, we believe in the power of doing things differently to make the impossible possible. Our people are driven by the desire to make the world a better place—to make a positive difference that contributes to a brighter future. We bring together technologies and industries, alongside the contributions of diverse individuals who are empowered by an intentional workplace culture, to solve problems better and faster. Key Responsibilities ControlST Embedded Software Validation for MarkVIe, IOPacks. knowledge of Bug Life Cycle (Visual studio TFS tool knowledge is a plus) Hands on experience in using instruments (Function Generator, DMM etc.) Test execution / development in visual studio (C# / spec flow). Should be able to analyse the failures in the script. Desired Characteristics Experience with Control Systems firmware validation for MarkVIe. Experience working with Industry protocols like MODBUS, Profibus, Profinet, FF, CAN, Ethernet Self-starter, able to work with multi-functional teams (Hardware, Software, System Test. etc.) Good interpersonal skills. We are known for our extraordinary people who make the impossible possible every day. Questians are driven by hunger, humility, and aspiration. We believe that our company culture is the key to our ability to make a true difference in every industry we reach. Our teams regularly invest time and dedicated effort into internal culture work, ensuring that all voices are heard. We wholeheartedly believe in the diversity of thought that comes with fostering a culture rooted in respect, where everyone belongs, is valued, and feels inspired to share their ideas. We know embracing our unique differences makes us better, and that solving the worlds hardest engineering problems requires diverse ideas, perspectives, and backgrounds. We shine the brightest when we tap into the many dimensions that thrive across over 21,000 difference-makers in our workplace. Work Experience Qualifications/Requirements (must) B Tech/ BE in Electrical/Electronics/Computers Engineering Test engineer should have 6+ year of experience in testing & test script development. Significant knowledge in embedded testing.

Role and Responsibilities: 1. Collaborate with design and architecture teams to understand SoC design and create validation plan to uncover Si issues 2. Develop and maintain firmware for CPU for functional bring up and validation 3. Debug Silicon issues in collaboration with HW teams to identify root cause. Skill Requirements: 1. Experience in Si bring up and pre-Si or post Si validation 2. Excellent C programming skills 3. Experience in Si debug using T32, JTAG and awareness of debug methodologies Good to have: 1. Experience in bringing up CPU on Post Si and on emulation 2. Knowledge of SoC architecture, ARM architecture and boot flows 3. Experience on firmware development for bare metal platform Experience: 5+ years of experience in Si validation and firmware development

Conduct Gas chromatography analysis of Pharmaceutical Samples To perform Validation of analytical methods To maintain all records as per cGLP and ISO 17025. Perform periodic calibration of Instruments/Equipments in Lab Preparation and Maintenance of standards

As a Program Manager for water purifier products, you will be responsible for leading New Product Introduction (NPI) projects from concept to launch. You will own project timelines, cost targets, and quality metrics throughout the product lifecycle. It will be your duty to establish clear program governance, conduct stage-gate reviews, and implement risk management frameworks. Collaboration with cross-functional teams including R&D, design, sourcing, manufacturing, quality, service, and marketing will be a key aspect of your role. You will align stakeholders to meet product specifications, regulatory standards, and customer requirements. Engaging with suppliers and vendors during development and ramp-up phases will also be part of your responsibilities. You will ensure that Design for Manufacturing & Assembly (DFMA) and other design principles are incorporated early in the design process. Supervising prototyping, pilot builds, and validation testing for performance, reliability, and regulatory compliance will be essential. Additionally, you will lead issue tracking and resolution during EVT, DVT, and PVT phases. Preparing for production readiness with manufacturing teams, optimizing costs through value engineering, and ensuring a smooth handover to operations post-launch are critical tasks. Continuous improvement of NPI processes, tools, and best practices tailored for consumer appliance development will also fall under your purview. Monitoring post-launch performance metrics and driving iterative improvements will be part of your ongoing responsibilities. Key skills and competencies required for this role include strong program management abilities, a deep understanding of appliance product development (preferably in water purifiers/home appliances/consumer electronics), knowledge of various components and processes, hands-on experience in DFMA, validation testing, and regulatory certifications, as well as excellent problem-solving, stakeholder management, and leadership skills. Strong communication and documentation abilities are also essential. In this role, you will have the opportunity to lead and influence the Native water purifier product line within a fast-growing organization. You will have a high-impact position with visibility across leadership and various cross-functional teams. The work culture is described as entrepreneurial and innovation-driven, offering you a dynamic and challenging environment to thrive in.,

As a Systems Engineer at our Electronics Manufacturing Cluster in Jabalpur, M.P., you will play a crucial role in designing and developing new products while also supporting and sustaining existing ones. Your responsibilities will include working on the design and integration of Battery System Architecture, encompassing electronics and electrical design. Additionally, you will be involved in verification and validation testing development, ensuring that design documentation is meticulously archived. Your role will also involve driving product enhancements and innovations to contribute to the exponential change towards electrification. With our pilot manufacturing line of 100MWh successfully operational, we are at the forefront of innovating in core battery design and are gearing up to rapidly scale our offerings and production in the near future. Being part of our team means having the opportunity to shape the future of ENERGY by thinking differently and contributing your passion and skillset to this dynamic sector. We are committed to providing you with a rewarding and agile environment that supports your professional growth and success on this transformative journey. If you are excited about making a meaningful contribution in the field of electrification and possess the necessary passion and skillset, we invite you to join us as a Systems Engineer in Jabalpur, MP.,

To check and monitor the GMP and GLP compliances. Dispatch of goods from plant - completion of all documentation and give the batch release To be responsible for overall quality assurance functions in the factory. To approve and monitor all SOPs related to QA, QC, Production, stores, Admin and Engineering departments. To approve all specifications of Raw Materials, Packing Materials, Intermediates and Finished Goods. To review and approve Validation Master Plan, Master Formula Records, Master BMR, Master BPR, Site master files. To approve and monitor all process validations, Cleaning validations, Hold Time Studies, Validations of premises, equipment and procedures. To approve the stability programme and procedure. To carry out the internal and external audits and to monitor the compliances of regulatory audits. To release the finished product after verifying the Batch manufacturing and packing records, analytical records and other related documents thereof. To design and approve the training schedule & impart training to all personnel. To check and approve the preventive maintenance schedule. To check for the sanitation of premises and equipment, hygiene & housekeeping of factory. To check and approve deviations, change controls, OOS, Investigation reports, all IPQA records and annual product reviews. To handle market complaints, FDA related matters and FDA complaints, product recalls and quality management systems activities. To monitor compliances for systems and documents and ensure all legal standards are met. To monitor the effectiveness and efficiency of HVAC, water system, Compressed air and all utilities used in the manufacturing of products. To monitor the formulation development and technology transfer activities from R&D and ADL To Confirm Quality Assurance at every stage of Product Processing. Responsible for handling and monitoring of control samples and upkeep of control samples room.

Responsibilities Lead designing and architecting Test Strategies and solutions along with their execution with other team members. • Co-develop, strategize and lead projects in manufacturing space to create low cost, highly efficient and sustainable processes within Zebra adopted framework of Industrial standards. • Test software development along with hardware design of manufacturing test systems for calibration & functional testing of electronic devices and opto-mechanical electronic products. Such products include specialty printers, mobile computers, laser & imaging scanning products. • Document test solutions, drawings, schematics and specifications as per departmental practices. • Perform Measurement validation and acceptance criteria using Measurement System Analysis (MSA) tools to validate the designed test system (Cpk, GR&R). • Support product testing during the New Product Introduction (NPI) phase as well as sustaining support. • Lead in Benchmarking test solutions to latest technologies and trends in manufacturing environment with the goal to improve product quality, line efficiencies and throughput within LSS and I4.0 Framework • Makes changes to or upgrades existing systems. Enhances and improves existing technologies to apply to new solutions seeking new tools to analyze and solve problems. • Be able to exchange ideas and articulate designs for test systems with peers and others in solution architecture Qualifications - Key Skills and Competencies: Expert in (5+ yrs.) Python scripting, Labview, C++ Minimum 2 yrs of experience in use of Data analytics tools and development – Power BI/Looker Expert in Technical analysis with problem-solving capability associated with the manufacturing or functionality of electronic systems • Licenses/Certifications, special qualifications: S/W development - training certifications

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview As a Test and Validation Engineer for TE Connectivity you will focus on test system design and verification-validation testing of high-speed products in cable assemblies targeting high speed communications and connectivity within datacenters and wireless infrastructure. You will be expected to independently work on projects in the areas of validation for product, test system design including selection of hardware and programming. You will work collaboratively within a broader cross functional team of electrical, mechanical, manufacturing, & operations to execute leading edge products designs. You will be the responsible for the electrical validation of a product/platform beginning with the initial analysis and leading into production verification testing and manufacturing. You will tackle challenging design problems and utilize cutting edge hardware and software tools to guide complex designs toward success. Responsibilities Responsibilities Subject matter expert in high-speed test systems and validation activities through product development cycles Testing, performance enhancement, and validation of high-speed cable assemblies using BERTs, network switches, traffic generators, etc. Establishing testing requirements for new products based on electrical and software specifications Development of high-speed cables test systems/fixtures from conception to manufacturing deployment Test system architecture, system diagramming, test software, hardware build, and validation into manufacturing of product Creating actionable recommendations based upon design reviews and product specifications Making data driven decisions about the product functionality and areas for improvement. Required Skills Bachelors degree in Electrical Engineering, Masters degree preferred Minimum of 10+ years of work experience in a high-speed test engineering role Experience with cable/cable assembly designs (high speed twin-ax cables, direct attach copper (DAC) cables, active copper cables) Experience with high speed test equipment (Digital Sampling Oscilloscope, Vector Network Analyzer, Bit Error Rate Tester, TDR, Pattern Generators, Power Supplies, etc.) Strong experience with Python Strong analytical capabilities to interpret test/lab data to identify issues and provide solutions to fix identified problem. Experience in project leadership, especially as it applies across design, development & manufacturing teams Excellent verbal and written communication skills Ability to work in a global environment able to accommodate varying time zones, fluent in English (verbal/written), able to collaborate with individuals across geographies Individual must be highly motivated, a quick learner, and able to work independently Nice to have Skills/Experience: Familiarity with embedded systems and ANSI C Familiarity with NI Test Stand Familiarity with signal conditioning techniques (equalization, amplification, FIRs, CTLEs) Familiarity with SFF/IEEE specifications for high speed cable assemblies Familiarity with PAM4/8 and other higher order modulation techniques Six Sigma methodologies or other strong data analytics background a PLUS Competencies

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview As a Test and Validation Engineer for TE Connectivity you will focus on test system design and verification-validation testing of high-speed products in cable assemblies targeting high speed communications and connectivity within datacenters and wireless infrastructure. You will be expected to independently work on projects in the areas of validation for product, test system design including selection of hardware and programming. You will work collaboratively within a broader cross functional team of electrical, mechanical, manufacturing, & operations to execute leading edge products designs. You will be the responsible for the electrical validation of a product/platform beginning with the initial analysis and leading into production verification testing and manufacturing. You will tackle challenging design problems and utilize cutting edge hardware and software tools to guide complex designs toward success. Responsibilities Responsibilities Subject matter expert in high-speed test systems and validation activities through product development cycles Testing, performance enhancement, and validation of high-speed cable assemblies using BERT s, network switches, traffic generators, etc. Establishing testing requirements for new products based on electrical and software specifications Development of high-speed cables test systems/fixtures from conception to manufacturing deployment Test system architecture, system diagramming, test software, hardware build, and validation into manufacturing of product Creating actionable recommendations based upon design reviews and product specifications Making data driven decisions about the product functionality and areas for improvement. Required Skills Bachelor s degree in Electrical Engineering, Master s degree preferred Minimum of 10+ years of work experience in a high-speed test engineering role Experience with cable/cable assembly designs (high speed twin-ax cables, direct attach copper (DAC) cables, active copper cables) Experience with high speed test equipment (Digital Sampling Oscilloscope, Vector Network Analyzer, Bit Error Rate Tester, TDR, Pattern Generators, Power Supplies, etc.) Strong experience with Python Strong analytical capabilities to interpret test/lab data to identify issues and provide solutions to fix identified problem. Experience in project leadership, especially as it applies across design, development & manufacturing teams Excellent verbal and written communication skills Ability to work in a global environment - able to accommodate varying time zones, fluent in English (verbal/written), able to collaborate with individuals across geographies Individual must be highly motivated, a quick learner, and able to work independently Nice to have Skills/Experience: Familiarity with embedded systems and ANSI C Familiarity with NI Test Stand Familiarity with signal conditioning techniques (equalization, amplification, FIR s, CTLE s) Familiarity with SFF/IEEE specifications for high speed cable assemblies Familiarity with PAM4/8 and other higher order modulation techniques Six Sigma methodologies or other strong data analytics background a PLUS Competencies Location

Hardware Engineer a) Functional testing of all Airtel Devices including Wifi, BT, BLE etc. b) Hardware Testing of Video platforms (like Android, Connected STBs etc.), GPON routers, 5G Devices, Power Adaptors, POE etc. c) Component level Analysis and verification from Prototype to pre-production as well as MP products. d) Handling of Testing Equipments such as CRO, Multimeter, Signal Generators and Power supply AC & DC Loads, Thermal Chamber, Wifi and BT testers. Analytical and Logical Thinking. Willingness to learn new upcoming technologies.

Key Role and Responsibilities: Should have experience in CSV (Computer System Validation) in Life Sciences domain. Should have good knowledge of GxP regulations and GAMP 5 Guidelines. Should have a good knowledge of 21 CFR part 11 and EU Annex 11 regulations. Should have experience in defining the validation strategy, approach, and alignment with customer on QMS. Should have good knowledge of Good Documentation Practices. Should have experience in authoring of CSV deliverables such as Validation Plan, Test Plan, RTM, Test Summary and Validation Summary Report, GxP Assessments, 21 CFR Part 11 assessments and System Release Notice. Should have experience of Validating Safety Systems. Should have strong understanding of pharmacovigilance, regulations and guidelines for difference geographic location. Should have experience in reviewing the CSV deliverables such as IQ, OQ and PQ scripts. Experience of QA in FDA / EMEA regulated environment is preferred.

The Materials Engineer will be responsible for developing, testing, and evaluating materials used in the manufacturing of Steering and Driveline products. This role involves ensuring that materials meet the required specifications and standards, conducting research to develop new materials, and improving existing materials. You will work closely with cross-functional teams to ensure that materials are used efficiently and effectively in the production process. The safety, quality, and performance of the materials must be prioritized, with timely escalation of any risks. You will also develop and maintain comprehensive documentation for all materials used from the IMDS standpoint. Primary Responsibilities - Analyze customer requirements to create detailed material specifications. - Develop and test materials to ensure they meet required specifications and standards. - Conduct research to develop new materials and improve existing materials. - Communicate with global teams and customers for program and technical reviews. - Execute product development process assignments on schedule. - Participate in cross-functional team meetings. - Support production in the region and provide material engineering expertise for supplier development, manufacturing quality analysis, and customer requests. - Lead material-related problem-solving and root-cause analysis. - Support new business pursuit activities for material applications. - Support project cost and timing estimations & Continuous Improvement Process (CIP). - Understand validation requirements for materials and plan for internal and customer-specific testing. - Enhance current material systems with new technology based on future OEM requirements. - Ensure seamless communication and documentation between all stakeholders. - Develop and maintain comprehensive material documentation throughout the product lifecycle. - Leverage knowledge of local supplier bases and competitor material landscapes to make informed design decisions. - Conduct thorough analysis of field failures and implement corrective & preventive measures. - Witness and understand various tests at both component and system levels. - Apply NVH (Noise, Vibration, and Harshness) basics to ensure optimal material performance. - Understand and implement testing requirements to meet customer and industry standards. - Collaborate with manufacturing teams to understand and optimize material processing techniques. - Stay updated with the latest developments and research in materials science, including nanomaterials and advanced manufacturing techniques. - Evaluate the sustainability and environmental impact of material choices. - Ensure compliance with industry standards and regulations (e.g., REACH, RoHS). - Perform cost-benefit analysis for material selection and processing methods. - Manage projects, including timelines, budgets, and resource allocation. - Collaborate with other engineering disciplines to integrate materials into product designs. - Use software tools for material simulation and data analysis. - Collate information for all product lines and coordinate with suppliers for entering data into the iPoint database. - Prepare IMDS reports for PPAP submissions to customers. - Ensure accurate and timely submission of IMDS data to meet customer and regulatory requirements. - Maintain up-to-date knowledge of IMDS regulations and best practices. Core Responsibilities - Ensure seamless communication and documentation between all stakeholders. - Develop and maintain comprehensive material documentation throughout the product lifecycle. - Support product validation activities and perform design reviews. - Collaborate with the Quality, Manufacturing, and Procurement teams to ensure that materials meet requirements. - Assist in problem-solving and troubleshooting to resolve material, manufacturing, or customer issues.,

6+ years of experience in Tosca automation testing. Knowledge of test automation frameworks and methodologies. Experience with API testing and database validation. Proficiency in defect tracking and test management tools. Write and execute test cases

As a Senior Battery Test Engineer, you will be responsible for designing experiments and fixtures, conducting battery-related test work, and documenting the results. Your role will involve applying first-principal engineering to new applications and collaborating closely with a team to deliver high-voltage architecture. Your key responsibilities will include preparing DFMEA, DVP&R, conducting RCA & FTA, and providing necessary support to the design team, battery prototyping, and battery production team. You should have a diploma or a bachelor's degree in Mechatronic, Electrical & Electronics, Mechanical, or equivalent field with relevant experience in high voltage Li-ion battery pack validation. To excel in this role, you must have a strong understanding of electrical-overcharge, force discharge, short circuit, imbalance charging, and other validation aspects. Experience in developing DVP based on industry standards and internal requirements is essential. You should be skilled in tear down analysis, using tools such as DMM, Oscilloscope, vibration shaker, climatic chamber, and various battery testers. Your expertise in vehicle-level validation, BMS functionality validation, battery prototyping, and data logging will be valuable. A solid grasp of electrical theory, mechanical structural failure theory, and the ability to design fixtures and conduct basic fabrication are required. You should be comfortable working independently with minimal oversight and possess skills in data processing for CAN and temperature data. Overall, this role requires a proactive individual with a keen interest in battery technology, vehicle testing, and validation processes.,

Test EV chargers (AC/DC) as per specs, set up stations, run diagnostics, log issues, ensure IS/IEC/BIS compliance, document reports, support R&D, update test SOPs, and maintain test equipment health. Required Candidate profile Diploma/BE in Electrical/Electronics with 1–4 yrs in product testing. Knowledge of EV chargers, testing tools, diagnostics, IS/IEC/BIS standards, troubleshooting, & basic SAP/MS Office skill required.

Roles and Responsibilities Lead the development team for UPS-INVERTER products, ensuring timely delivery of high-quality solutions. Design and develop power electronics systems, including PCB testing and validation using MATLAB simulations. Collaborate with cross-functional teams to integrate hardware design, software development, and automation testing. Develop test plans, procedures, and reports for new product launches. Conduct relay testing and application testing to ensure product reliability and performance. Desired Candidate Profile 10-20 years of experience in Power Electronics industry with expertise in Inverter technology. Bachelor's degree in Engineering (B.Tech/B.E.) from a recognized university. Strong knowledge of electrical testing tools such as oscilloscopes, multimeters, etc., as well as proficiency in PCB testing techniques.

Roles and Responsibilities Design, develop, test, and validate power electronics systems using MATLAB and Simulink. Conduct hardware testing of inverters, PCBs, relays, and other electrical components. Collaborate with cross-functional teams for application testing and validation. Troubleshoot issues related to power electronics systems using debugging techniques. Develop automated tests using various testing tools to ensure efficient testing processes. Desired Candidate Profile 4-9 years of experience in UPS Testing Engineer role or similar position. Bachelor's degree in B.Tech/B.E. (Computers) or B.Tech/B.E. (Electrical). Strong knowledge of power electronics principles, including inverter design and operation. Proficiency in PCB testing, relay testing, and automation technologies such as MATLAB/Simulink.

As an experienced and dynamic Validation Lead/Manager with 8-12 years of experience, you will be responsible for overseeing validation activities to ensure compliance with Good Practice (GxP) standards, including GLP, GCP, and GMP. Your role will involve managing validation teams, driving the validation strategy for key projects, and ensuring regulatory compliance. Your key responsibilities will include leading the validation team in maintaining GxP compliance, developing and implementing validation strategies, supervising and mentoring validation engineers/specialists, overseeing the development and approval of Computer System Validation (CSV) documentation, leveraging product knowledge in life sciences and Healthcare products, staying updated on regulatory changes, collaborating with cross-functional teams, conducting training sessions, and managing validation projects. To excel in this role, you must possess leadership and management skills, project management expertise, knowledge of GxP compliance, familiarity with regulatory requirements and industry standards, understanding of quality management systems in R&D environments, expertise in validation testing and CSV principles, and hands-on experience with life sciences products such as eQMS, eTMF, RIM, CTMS, Argus, RAVE EDC, or similar systems. Qualifications for this position include a Bachelors or Masters degree in a relevant field, a minimum of 7 years of experience focusing on GxP, validation testing, and CSV, strong analytical and problem-solving skills, excellent communication and collaboration abilities, and the ability to lead, mentor, and motivate a team.,

Walk-In Drive For API Plant Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 30-08-2025. Requirement for Executive / Senior Executive - API Plant AR&D - API Analytical Research & Development(AR&D) HPLC,GC API QC Experience also Consider High performance liquid chromatography (HPLC) & GC HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance API QC Experience also Consider Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines and execution through proper protocols. Compliance of Good Laboratory Practice in the lab Responsible for providing support to technical issues related to R&D to file the Drug Master files. Effective method development ensures that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery time-lines and adherence to quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues and communicating conclusions from stability studies. Interview Date : Saturday 30-08-2025 Department : Plant Analytical Research & Development(API AR&D) HPLC,GC API QC Experience also Consider Experience : 1 to 6 Years Qualification : M.Sc Position: Executive / Senior Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details :Venue Details : MSN Laboratories Pvt. Ltd, R&D Centre, Pashamylaram (V), Patancheru (M), Sangareddy (D.t), Telangana