34 tester jobs found for you.

. Experience in Javascript/Java with Playwright2. Experience in BDD framework3. Strong experience in Automation and Manual Testing4. Good knowledge in CICD process5. Good to have Medical Device Software experience experience7

Senior Automation Testing experience10

Key Responsibilities Architecture & Designo Contribute to the design of scalable, maintainable QA automation frameworks for API, UI, integration, andperformance testing.o Implement automated test scenarios across microservices, APIs, data workflows, and distributed systems.o Participate in design discussions to ensure testability, document risks, and propose automation strategiesaligned with engineering standards. Engineering Excellenceo Produce clean,

Hi Please find the below skills listed to be discuss on call Here is what will be discussed on the call:Senior Test Automation Engineer – JobDescription Job Summary:We are looking for a highly experienced and strategic Principal Automation Test Engineer tolead and drive our test automation strategy across complex systems, with a primary focus onour new business critical Integration platform. This role involves planning, executing, andreporting on various

Experience (in years): Five (5) YearsProduct Experience & Technical Expertise:1)Architect, design, and develop automated EOL (End-of-Line) test systems for automotive electronic products— (infotainment, telematics, ECUs, sensors, switches, and control modules.)2)Develop ATE software architecture including:LabVIEW-based test sequences, GUIs, and hardware abstraction layers.Python/C/C++ modules for device communication, business logic, and data

Experience: 5+ years of experienceQualifications: Bachelor’s degree, preferably B.E / B. TechTechnical Skills:• Strong background in, and at least 3+ years of working in QA automation• Experience in programming languages like Java, Python, or C++• Experience in writing, executing and monitoring automated test suites using a variety oftechnologies including, but not limited to, Cucumber, Concordion, Selenium, Fit/FitNesse, SoapUI• At least 2 years of

Role:  • Lead and manage procurement process for all material and service requirements of MBD• Establish procurement processes including analyzing market, reviewing supplier base, setting pricing structure, benchmarking with competitors and supplier management• Float RFPs to existing and potential suppliers in case of new material / service requirements• Oversee negotiations with approved suppliers for procurement within budget; closely monitor

• Lead the drafting and validation of Business Requirements Documents (BRDs) for allExchange applications including Trading, Surveillance, Listing, and Member interfaces• Oversee the creation and maintenance of User Manuals and operational documentation• Manage testing activities across multiple applications, including:o User Acceptance Testing (UAT) – functional and non-functionalo System Integration Testing (SIT)o Load & Performance Testingo Usability

Job Description: Group Leader – Assembly Maintenance (Permanent Role)Location: TKM, Bidadi, MaintenanceExperience Required: 9–12 yearsEducation: Diploma in Mechanical, Electrical, or Mechatronics EngineeringAge Group: 28–32 yearsTeam Size: Lead a team of approximately 8–10 subordinatesShift Pattern: 3 shifts weekly rotation, including holiday and shutdown workCore ResponsibilitiesFilling Equipment Maintenance: Lead the troubleshooting and preventive

Analytical Scientist II - Pharma/Biotech   Designation: Analytical Scientist II    Job Location: Bengaluru   Department: Analytical Research and Development - Complex injectables    Educational qualification: Bachelor’s or Master’s degree in Pharmacy or Chemistry     Experience:4 to 6 years (in Analytical research and development – Injectable drug products)       Behavioural skills:Should have the capability to work individually and in a team.Should have

Java Software Engineer About the Role:We are seeking a talented and passionate Java Software Engineer to join our growing team.In this role, you will be responsible for designing, developing, and maintaining high-performance Java applications.You will work closely with other engineers and stakeholders to deliver innovative and scalable solutions that meet our business needs.Responsibilities:Design, develop, and test Java applications using object-oriented

Job Details:   Title: Hardware Test Leader  EducaƟonal QualificaƟons: B.E. / B Tech /M Tech with Electrical/Electronics/Instrumentation.   Experience: Minimum 10-14 years of experience in Electronics Hardware development/TesƟng in the automoƟve  industry   Location: Bengaluru India Technical Center  Job Purpose:   As an experienced Hardware Test Lead, you will be involved in the verificaƟon and qualificaƟon of Power Electronics  Hardware design for

APAR INDUSTRIES LTDMANPOWER REQUISITION FORM (MRF)Job Description / Competency Profiling DesignationAsst. Manager / Dy. ManagerDate of requisition30th Oct, 2025 Company / Division / SBUTelecom Solutions(Project Kavach)LocationPurulia / Adra / Kharagpur, West Bengal Function / DepartmentProjectsWork Cadre(SMC/MMC/JMC/NMC)  Basic QualificationB.Tech / Diploma – Electronics & Communication/ Electrical / Telecommunication / Instrumentation

Key Responsibilities 1. Process Quality Control • Ensure adherence to defined quality standards across the production process. • Implement and monitor process verification checks on the shop floor. • Ensure proper documentation and records of all verification activities. 2. Product Verification • Verify production outputs to ensure quality standards are maintained. • Conduct sampling checks from production batches to validate product quality. • Ensure

1. Co-ordinating quality checks for process parameters as per desired frequency2. Ensuring product quality at standard with Quality best practices3. Prepare SOP and checklist of all quality process.4. Safety and upkeep of the assets of the organization5. Directly responsible RM PM testing.6. Ensuring Calibration of lab instruments.7. Ensure CCP monitoring and control.8. Responsible for NPD product trial quality compliance9. Responsible for daily shift

KEY RESPONSIBILTIES / WHAT WE EXPECT: ✓ Review of Aker Manufacturing record books to ensure technical & administrative correctness. for the assigned projects. ✓ Prioritise and manage assigned work. ✓ Ensure timely communication with stakeholders. ✓ Manage the progress of the MRB’s which are on hold. ✓ Support MRB DC’s on technical aspect of the Manufacturing Record Books. Provide training on  product and technical aspect of the documentation.  SKILLS AND

Key Responsibilities of the QSE1. Review of Supplier Documentation (70% of Time)Review pre-verification documents such as SMDL (Supplier Master Document List), ITP (Inspection and Test Plan), and Procedures received from the Supplier.Review verification documents against requirements from the PO (Purchase Order), Project/Client specifications, Material specifications, product specific requirements, and applicable codes & standards.Create a COM document in

Quality Documentation Expertise● Lead the implementation of automation for APQR (Annual Product Quality Review)preparation.● Support AI training and validation using real-world pharma quality documents.● Assist in automating documentation related to:○ APQR (Primary)Quality investigations (Secondary)○ Deviations and CAPA (Secondary)○ SOP documentation (Secondary)○ Quality reports and summaries (Secondary)experience5

We are looking to fill a Asst Manager- Quality position. I would like to seek your assistance in identifying suitable candidates for this role. Below are the details about this role, also attached JD for your ref. Position Summary-Looking for an Asst. Manager – Quality with 5–8 years of experience in managing Quality Management Systems (QMS) and EHS compliance. The role involves conducting internal and third-party audits, ensuring timely NCR closures, and

Key responsibilities:Oversee daily operations, manage personnel, and provide technical andstrategic direction for the QC department.Develop, implement, and maintain quality control systems and ensure allprocesses adhere to company standards and regulatory requirements.Supervise the analysis of raw materials, in-process samples, finishedproducts, and stability samples. Review analytical data, protocols, andreports. Thorough knowledge in handling all

Job Title - Condition Monitoring AnalystJob Description:Analyzes condition monitoring data (S·O·SSM, inspections, electronic data, site conditions, equipment history) and provides relevant recommendations for the customer as indicated by the data. Essential Duties and Responsibilities include  Analyze condition monitoring data (e.g. S·O·S, inspections, electronic data, site conditions, equipment history)Provide equipment and/or operation recommendations

QC Analyst (Contract) - Bengaluru, KarnatakaWe are seeking a proactive and detail-oriented QC Analyst to join our team in Bengaluru on a contract basis. This role is crucial for ensuring the quality and compliance of our products within the healthcare industry. If you possess strong analytical skills and a commitment to excellence, we encourage you to apply.Responsibilities:Perform routine analytical tests to ensure product quality and consistency.Conduct

Education: Bachelor's degree in a scientific or engineering discipline, or equivalent experience.Experience: 3-5 years of proven experience in QA review/approval of validation deliverables within aregulated industry, such as pharmaceuticals, biotechnology, medical devices, or otherrelevant sectors. Experience in computer system validation using GAMP 5   Experience in infrastructure qualification Experience with Quality Systems (e.g. change control,

Quality Associate- Nanded Purpose of the Role:Support the QA Team in the effective functioning of the QA department in alignment with defined quality systems. Evaluate incoming raw materials, intermediates, and finished products. Conduct routine testing of processed and incoming goods. Calibrate and maintain inspection, measuring, and testing equipment. Ensure raw and packaging materials meet defined standards. Ensure Safety at laboratory Conduct line

QA Associate - Contract - Mining - Odisha, IndiaWe are seeking a proactive and detail-oriented QA Associate to join our team on a contract basis within the mining sector. This is a fantastic opportunity for a qualified professional to contribute to our quality assurance efforts in Bhubaneaswar Pur, Odisha. If you have a strong background in quality assurance and a keen interest in the mining industry, we encourage you to apply.Responsibilities:Conduct

Senior professional in the QA / QS with additional experience in Tool Room domain  is advantage to take on the role of Head . This position will be responsible for Head of the quality. Job Responsibility :Incoming InspectionReview incoming raw material quality reportsApprove or reject incoming materials based on inspection findingsCoordinate with purchase and suppliers for material quality issuesEnsure compliance with supplier quality agreementsSupplier

Pre-funding Reviews: Audits conducted before loans are finalized to catch errors early.Post-closing Audits: Typically, a random sample of at least 10% of monthly production is reviewed within 90 days of closing to identify deficiencies.Compliance Checks: Ensuring adherence to regulations like TILA-RESPA, FDCPA, and ECOA.Servicing QC: Monitoring loan servicing activities, including escrow, payment processing, and loss mitigation.Technology

QA Incharge (Contract) - Steel Industry - Jamshedpur, IndiaWe are seeking a proactive and experienced QA Incharge for a contract position within the Steel industry in Jamshedpur, Jharkhand, India. The ideal candidate will possess a strong background in Quality Assurance and a minimum of 3 years of experience, with a maximum of 10 years, demonstrating a comprehensive understanding of quality control processes within a manufacturing

Greetings from Randstad ! Job DescriptionHaving knowledge Non non-destructive testing field.• Having knowledge in Heat treatment process & Post weld heat treatment process.• Self-dependent working style and analytical thinking.• Very good communication skills.• Self-motivated, self-starter, creativity and strong work ethic.• Good team player with the capability to work under pressure and maintain good rapport with teammembers.• Capability to learn and

QA head – Pharma Sterile Formulations Location: Jeedimetla Unit 2 Education : B. Pharm, M.Pharm or M. Sc related in pharmaceutical science  Experience: 10-15 years in Pharmaceutical QA with a strong preference for experience in sterile formulations.  Key Responsibilities Core experience in manufacturing of eye drops, ear drops and nasal sprays. Perform online monitoring and in-process checks during manufacturing, filling, and packing operations in aseptic