Quality Engineer Graduate Jobs in Navi Mumbai

An Erection & Commissioning Engineer is an engineer responsible for:Erection (Installation)Supervising installation of industrial equipment, machinery, pipelines, electrical systems, or plant structures.Ensuring equipment is assembled according to drawings and technical specifications.Coordinating with mechanical, electrical, civil, and instrumentation teams.CommissioningTesting and starting up systems after installation.Checking performance, safety, calibration, and operational readiness.Troubleshooting issues before handing over the plant/equipment to operations.

Job Description: Quality EngineerPosition Details Position Title: Quality Engineer Location: Khopoli - Pali Road Department: Quality / Operations Reports To: Assistant Sourcing Manager and Functionally to Assistant Customer Service Manager Employment Type: Full-timeLocation Preference Candidates residing in the Navi Mumbai or Khopoli region will be preferred or should be willing to relocate.Role Overview The Quality Engineer will ensure that all manufactured machines, assemblies, and spare parts meet inhouse drawing specifications and meet customer expectations. The role involves supplier quality improvement, shop-floor quality control, interpretation of OEM Belgium drawings. The engineer will coordinate closely with sourcing, production, and customer service teams, including handling quality or delivery risks related to new suppliers and ongoing orders. The role also includes supporting reliability analysis through run life calculations and Mean Time Between Failure (MTBF) evaluation for critical parts and complete machines, along with driving root cause analysis and continuous improvement.Work Distribution 60% Supplier Quality & Supplier Visits (initial phase) 40% Shop Floor Quality at Khopoli Note: This ratio will gradually shift toward more shopfloor focus as suppliers stabilize and the Khopoli factory becomes fully operational.Supplier Quality Conduct supplier evaluations, capability assessments, and audits. Work with suppliers to improve machining quality and implement robust process controls. Ensure suppliers correctly interpret engineering drawings, GD&T, tolerances, and material standards. Support suppliers in scaling up quality for complex, high-precision components.Typical QC Scope (Parts & Machines) Perform QC on machined parts such as tool holders, die holders, shafts, bushes, plates, brackets, fabricated assemblies, and other components related to group company enquiries. Understand machining processes including CNC Turning, CNC Milling, VMC/HMC, grinding, fabrication, bending, laser cutting, wire-cut EDM, etc. Evaluate secondary processes such as heat treatment, hardening, stress relieving, surface finishing, and other value-adding operations.Quality Management & Compliance Implement and maintain QA procedures, documentation, and reporting systems. Ensure compliance with ISO 9001, IATF 16949, ISO 14001, and customer standards. Maintain control plans, PFMEA, work instructions, and inspection documents. Support customer audits, internal audits, and compliance reviews.Inspection & Testing Conduct incoming, inprocess, and final inspections Use precision measurement instruments such as height gauge, vernier caliper, micrometer, bore gauge, and dial indicators. Verify material grades as per EN and IS standards. Analyze inspection trends to determine deviations and corrective actions.OEM Drawing Understanding & Technical Communication Extract key technical details from OEM Belgium drawings (GD&T, tolerances, fitment requirements). Coordinate with OEM engineering teams for clarifications. Recommend design modifications for cost reduction and enhanced manufacturability. Communicate technical requirements clearly to suppliers and internal teams.Root Cause Analysis & Problem Solving Apply structured methodologies such as 5 Why, Fishbone Diagram, 8D, and DMAIC. Lead crossfunctional teams to address quality issues. Drive implementation and verification of corrective and preventive actions (CAPA).Continuous Improvement Support lean manufacturing and wastereduction initiatives. Identify process capability improvement opportunities. Participate in capability studies including Cp, Cpk, MSA, and GRR.Qualifications & Requirements Degree in Mechanical, Production, or Industrial Engineering. 2-5 years experience in machining quality, supplier quality, or manufacturing QC. Strong knowledge of machining processes (CNC, VMC, fabrication, grinding). Handson experience with APQP, PPAP, FMEA, MSA, SPC, 8D. Proficient with precision measuring instruments. Strong understanding of EN & IS material standards. Ability to read and interpret technical drawings with GD&T. Strong communication skills for interaction with OEM Belgium. Experience with QMS/ERP systems is an advantage.Key Competencies Analytical and detailoriented Ownership and accountability Strong technical communication skills Continuous improvement mindset Customerfocused approachWhy Join Us? Fastgrowing and technically dynamic environment Opportunity to contribute to advanced manufacturing and quality systems Longterm growth and development opportunities

Monitor and ensure quality of construction work as per approved drawings and specificationsConduct site inspections, tests, and audits to ensure compliance with standardsPrepare and maintain quality documentation, reports, and checklistsCoordinate with site engineers, contractors, and consultants for quality-related mattersEnsure materials used at site meet required quality standardsIdentify defects and suggest corrective and preventive actionsEnsure compliance with BMC and other regulatory guidelinesMaintain records of tests (concrete, soil, materials, etc.)Participate in client/authority inspections

Job Position: Site SupervisorRequirement: Male Candidate below 40 yearsQualification: Diploma / BE in Mechanical Experience: Should have 3-5 years Key Objectives:To manage Fire Fighting projects from start to finish, and the responsibilities include: Safety: Ensuring the safety of all workers on site, including making sure they wear the correct protective equipment Quality: Ensuring that work is carried out to the required standards and specifications Cost: Controlling costs Deadlines: Meeting project deadlines Communication: Regularly communicating with project stakeholders, such as clients, suppliers, and architects Planning: Helping project managers plan work activities Organization: Organizing work schedules and managing teams of workers Procurement: Managing the procurement of firefighting materials and equipment Inspections: Regularly inspecting the on-going site Records: Completing site reports and other records Meetings: Attending site management meetings

Key Responsibility.Incoming material inspection.in-process Quality inspection.pre- Dispatch inspection.(PDI)Documentation.

We are hiring for Quality Engineer- Chemical A) Qualification : To become a QA person in the pharmaceutical industry, one should have a degree in a science-related field, such as chemistry or pharmacy, to better understand pharmaceutical products.B) Experience : 0 to 2 years in R&D Pharmaceutical Industry from QA Department.C) Responsibility :1. Review of Manufacturing Processes.2. Knowledge of All regulated Guideline & Pharmacopoeia.3. Preparation & implementation of SOPs related to the concerned department & Justification of Specification.4. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.5. QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.6. The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.7. A QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements8. The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.9. The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA).10. A QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.11. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.12. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.Qualification- Graduate in Chemical Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Job Description: Assist the sustainability lead to assess various plastic recycling technologies - Identify, understand, and evaluate plastic recycling technologies. To Identify opportunities in various biopolymer product/technology and bio composites. Assessment of various technology for sorting / segregation and cleaning of waste plastic for mechanical recycling Support for preparation of overview/prefeed documents for new projects Validate equipment data sheets prepared by consultant/ engineering contractor for various projects. Execute process design calculations for the various schemes. Assist to develop process design package using appropriate tools. Identify opportunities for product quality enhancement/ product upgradation. Participate in pilot / commercial plant trials. Understand and evaluate basic engineering design documents. Validate modifications to ensure specified standards and codes are followed in calculations. Participate in PHA/ HAZOP of new projects/ modifications. Contribute to derive value from technology network. Understand and be abreast with legislation/ regulation as and when mandated by CPCB/ MoEF, GoI.Skills and Competencies Sound knowledge regarding polymerization process and technology. Knowledge on polymer product, processing, and applications. Experience in polymer plant operation / technical service domain Knowledge of chemical engineering and process technology Ability to plan / discuss results and network under the guidance of senior colleagues. Process design calculations at Skill level Use of process calculation templates at Skill level Process simulation skills Use of Six sigma for problem solvingEducation RequiredBE/B Tech in Chemical Engineering from a reputed instituteMBA will be added advantage.Experience Required3 to 4 years of experience with at least 2 years in plant Operations / CTS

Production Manager position. Looking after daily production of medical devices and following SOP and maintaining QMS as per required. Looking after waste management, production management, raw material management and quality assurance in production. Looking after production time frame for dispatch

1.Analysing information received from stakeholders to plan and execute software development for varying needs2.Finding bugs and fixing them to ensure the software runs without errors3.Developing and implementing new techniques for testing and validating software systems4.Guiding the software programming efforts5.Directing the compilation of the documentation6.Communicating project statuses and proposals in close collaboration with clients and other internal departments7.Exploring the areas for improvement and constantly developing the user experience by adding new features8.Maintaining and enhancing current codebases, and peer-reviewing code modifications, Ecommerce expertise,API integration,aws deployment ,serializer.

Job title QA & QC - Quality Assurance & Quality ControlSalary 2.82 LPA & Based on experience and last drawn CTC.Shift Required GeneralQualification BE Mechanical /B.TechGender - FemaleDesignation Quality Engineer/ Quality TraineeExperience Minimum 1 Year ExperienceVacancy- 01Roles & Responsibilities Inspection of end fittings as per sampling plan, Drawing and SO. Reporting of Lot acceptance or rejection of individual lot/ GRN Decision on rejected Lot by concerning with Asst Manager- QA Assembly Information to Purchase Head, QA Head and Planning Head Review supplier MTC received along with documents for end fitting with standard or specification. In case MTC is not received, inform to purchase immediately. Supplier visit as and when required. SAP working Raise the Internal NC. Knowledge of 7 Quality Tools Technical Knowledge of ISO 10380:2012 Knowledge of ISO systems related to QAThanks & Regards, Human Resource - Executive

Hiring for 1 Mechanical Engineer Job in midc taloja, AutoCAD Designer, Quality Assurance Incharge, Quality Assurance Inspector, with minimum 3 Years Experience, Required Educational Qualification is : B.Tech/B.E with Good knowledge in AutoCAD, Mechanical Maintenance, Mechanical Electrical Plumbing, Mechanical Testing, Mechanical Metallurgy, AutoCAD Designer, Quality Assurance Incharge, Quality Assurance Inspector etc.,

Required Skills:No degree/qualification requiredStrong Java programming skills and OOPS conceptsBasic knowledge on QA testing methodology and toolsBasic knowledge of Selenium web driver.Decent understanding of QA automation on web, mobile and APIBasic knowledge of using git and shell scripting.Decent understanding of performance testingRoles and responsibilities:Will be working as a freelancer and should be able to devote atleast 25 hours/weekFlexible working hoursWill be required to do both manual and automation QAAnalysing/preparing test cases and debugging defects.Automation responsibility - developing test scripts/framework using Java for web/mobile/APIs.Performance testing of web based applicationsDecent understanding of performance testingSince this is a freelancing role - no laptop/machine will be provided for the same.Highest qualificationYears of experience into QA/Dev if any?Expected salary/monthLink to github or any open source contribution (if any)Configuration of the machine/laptop which you will be using to workLatest CV

Job Accountabilities Process & Quality Monitoring For Respective Technology Plants Identify And Analyse Deviations Perform Root Cause Analysis Propose Corrective Action And Track The Status Of Process Improvement Identify Opportunities For Profit Improvement Identify Opportunities For Product Quality Enhancement Process Design Calculations For The Improvement Schemes Develop Process Design Package Using Appropriate Tools Participate In Commercial Plant Trials Understand And Evaluate Basic Engineering Design Documents Participate In Plant Performance Audits As Per Set Guidelines Participate In Critical PHAs And Turnaround Activities Of The Related Plants Validate MoCs To Ensure Specified Standards And Codes Are Followed In Calculations Support Preparation Of Stage Gate-2 And 3 Document For Capital Projects Participate In HAZOP Of New Projects Validate Equipment Data Sheets Prepared By Engineering Contractor Contribute To Derive Value From Technology NetworkSkill & Competencies Analytical Ability For Problem Solving Programming Exposure Knowledge Of Chemical Engineering And Process Technology Ability To Plan / Discuss Results And Network Under The Guidance Of A Senior Colleagues Process Design Calculations At Skill Level Use Of Process Calculation Templates At Skill Level Simulation Skills Use Of Six Sigma For Problem Solving Good Communication Skills Leadership Quality With Management Skills Result OrientationEducation Required Bachelors Or Master's Degree In Chemical EngineeringExperience Required Operations / Technology Experience Of EOEG / MEG Plant Will Be Preferred 8 To 13 Yrs Of Relevant Experience

Designation : QA ManagerLocation : MumbaiQualifications : Degree in a science-related field, chemistry or pharmacyExperience : 3+ years in R&D Pharmaceutical Industry from QA DepartmentResponsibility :* Review of Manufacturing Processes.* Knowledge of All regulated Guideline & Pharmacopoeia.* Preparation & implementation of SOPs related to the concerned department & Justification of Specification.* Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.* QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.* The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.* QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements* The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.* The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA)* QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.* Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.* Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.* Implementation & verification, in-process checks, online entries in BPR of product at Pilot plant manufacturing site.* Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site.Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Need a candidate who has good amount of production management knowledge with minimum 5 to 6 years of experience in the same field. He should have qualities like Production control, quality control, stock management waste management, error control, costing control, QMS, SOP, 5 P of production. production staff management. We looking for candidate for long term for at least 5 years.