Senior QC Engineer

Arviups; Bengaluru; On-site; INR 670,000 - 1,116,000; Full time

Job summary

Arvi Systems and controls Pvt Ltd in Bengaluru requires a Senior QC Engineer with 3–5 years of hands-on QC experience in EMS/electronics manufacturing. You will own product quality and reliability across UPS production, audit QC inspections, and drive CAPA and supplier quality improvements.

The role involves in-process QC, FAT, supplier audits, and continuous improvement. 3–5 years’ experience and BE in Electronics/Electrical are mandatory; female candidates may also apply.

Qualifications

• BE in Electronics or Electrical is mandatory.
• 3–5 years of hands-on QC experience in EMS/electronics manufacturing is mandatory.
• ISO quality documentation, internal auditing, non-conformance management and CAPA are required.
• Continuous improvement mindset; male preferred, female candidates considered.

Responsibilities

• Hands-on in-process quality control and inspection of UPS parts assembly.
• Verify workmanship and conformity to drawings, specs, procedures and checklists.
• Audit in-process QC and ensure corrective actions are implemented.
• Conduct FAT before dispatch and document deviations and retesting outcomes.
• Lead supplier quality improvements and ensure acceptance testing and NC closure.

Skills

QC Experience

Electronics

Audit Capability

CAPA

Education

BE in Electronics/Electrical

Job description

Yeshwanthpur industrial suburb, Bangalore 3–5 years Electronics manufacturing QC Salary up to ₹1,00,000

Own product quality. Strengthen processes. Drive reliability.

Position overview

Company : Arvi Systems and controls Pvt Ltd

Experience : 3–5 years of relevant hands-on QC experience in an EMS (ElectronicManufacturing Services) or electronics manufacturing company – (mandatory)

Qualification: B.E. in Electrical or Electronics Engineering – (mandatory)

Attractive salary and benefits; salary upto Rs.1,00,000.00

Role Purpose

Take ownership of product quality and reliability across electronic manufacturing andindustrial UPS production. This role requires hands-on technical knowledge to verify andaudit inspections carried out by QC personnel, oversee in-process quality controls, conductsupplier conduct pre-dispatch acceptance testing, and ensure effective follow-through onfailure analysis and corrective and preventive actions across departments.

Drive supplier quality improvement through process audits, incoming non-conformanceanalysis, root-cause identification, and implementation and verification of corrective andpreventive actions at the supplier’s premises to prevent recurrence and ensure consistentincoming material quality.

Qualifications and Experience

• B.E. in Electronics, Electrical, Instrumentation or a related electronics discipline.Mechanical engineering qualifications are not suitable for this role.
• 3–5 years of relevant hands-on QC experience in an EMS (Electronic ManufacturingServices) or electronics manufacturing company. Prior experience in electronicsmanufacturing is mandatory.
• Practical experience in ISO quality documentation, internal auditing, non-conformancemanagement, corrective and preventive action (CAPA), and continuous improvement ismandatory.
• Male candidates preferred; suitably qualified female candidates will also be considered.No specific language requirement.

Key Responsibilities

Hands-on in-process quality control. Conduct physical inspection of UPS parts assembly,wiring, testing, heat-run and pre-dispatch QC. Verify workmanship and conformity to approveddrawings, specifications, procedures and inspection checklists. Identify and address qualitygaps at the stage where they originate.

Verification and audit of in-process quality. Recheck and audit inspections carried out bydesignated QC personnel for bare PCB, PCB assembly and soldering. Verify workmanship,inspection accuracy and conformity to approved drawings, specifications and procedures.

Conduct unannounced, sample-based reinspection of previously QC-approved items to identifymissed defects and verify the effectiveness of existing QC checks. Provide guidance andensure corrective action for identified gaps.

Factory acceptance and dispatch clearance. Conduct and document Factory Acceptance Tests(FAT) before dispatch. Verify required electrical, functional, performance and safety checksagainst approved test procedures and acceptance criteria. Record deviations, coordinaterectification and retesting, and confirm quality clearance before dispatch.

Failure analysis and quality feedback. Document internal failures, test failures andfield-return feedback. Work with the concerned teams to identify root causes and determinewhether the issue relates to design, PCB fabrication, soldering, assembly, testing or aquality-control gap. Translate findings into specific actions for the responsibledepartment.

Quality Actions and Reliability Ownership

Department-specific improvements. Coordinate necessary work instructions, process controls,drawing revisions, test procedure improvements, inspection criteria, ISO document updatesand targeted employee training. Ensure approved changes reach the relevant department and are implemented at the point of use.

Corrective and preventive action. Assign and track action owners, target dates,implementation progress and evidence of completion with the concerned departments. Progressively monitor implementation, verify effectiveness and prevent recurrence. Closeactions only after implementation and effectiveness have been confirmed.

Immediate flagging of non-conformances. Immediately flag and highlight every identifiednon-conformance (NC) to the concerned department and management. Maintain its open andflagged status until it is resolved and verified. Escalate overdue, recurring or unresolvedissues and ensure suitable containment of affected products.

ISO documentation and auditing. Maintain controlled quality records, failure-analysisreports, NC registers, CAPA records, inspection and FAT reports, audit findings and trainingrecords. Conduct process and documentation audits, follow up findings and keep relevantquality-system documents current.

Continuous improvement and reliability. Review recurring defects, failure trends and processweaknesses. Drive measurable improvements in manufacturing quality and product reliability,verify that revised controls are followed, and report unresolved risks and action status tomanagement.

Supplier Quality and Incoming Material Control

Own the quality of purchased materials and outsourced processes from PO specificationsthrough supplier manufacture, incoming verification and confirmed corrective-action closure.Prevent defects at the supplier’s premises and build confidence in supplier QC approval andtest reports.

Technical specifications and PO quality requirements. Work with engineering and procurementto strengthen specifications issued with purchase orders. Define applicable electricalratings, tolerances, materials, workmanship criteria, inspection and test parameters,acceptance limits, drawing revisions, traceability and mandatory test-report requirements.Ensure suppliers understand and use the approved requirements and obtain approval beforechanging materials, processes or specifications.

Incoming inspection controls. Strengthen incoming QC for raw materials, components,subassemblies, sensing transformers, power transformers, capacitors, bare PCBs andoutsourced PCB assemblies. Identify additional checks needed from failure history andquality risks. Maintain current inspection drawings, checklists, work instructions, testprocedures and acceptance criteria, and verify that incoming QC personnel apply themcorrectly.

Supplier process improvement. Visit suppliers to review their manufacturing, inspection andtesting controls. Investigate defects at their source, including outsourced wave solderingand manual soldering. Agree and drive improvements to supplier procedures, drawings, workinstructions, process settings, inspection methods and personnel training to preventdefective material from reaching Arvi Systems.

Incoming non-conformances and root causes. Immediately flag incoming NCs, contain affectedmaterial and escalation to the supplier, procurement and concerned technical teams. Requiredocumented root-cause analysis and corrective and preventive actions; visit the supplierwhen needed to validate the cause. Set action owners, implementation targets and completiondates, and keep NCs open until actions and effectiveness are verified.

Implementation verification and supplier audits. Monitor supplier action plans and verifyimplementation through follow-up visits, re-audits and unannounced audits where accessarrangements permit. Check that agreed process changes, document revisions, training andquality controls are actually followed. Verify sustained effectiveness in subsequentsupplies and elevate recurring or overdue issues.

Supplier test reports and independent rechecks. Require relevant inspection and test reportswith each supply, traceable to the supplied lot or items and stating actual results againstspecified acceptance limits. Randomly recheck selected reported parameters and QC-approveditems to confirm report accuracy. Raise an NC for any discrepancy, investigate its cause andrequire correction of both the product and the reporting or testing process.

Supplier accountability and evaluation. Evaluate suppliers against quality, repeat defects,test-report accuracy, responsiveness, adherence to specifications and commitment tocorrective actions. Recommend applicable rejection, replacement, rework-cost recovery orpenalties through procurement and management in accordance with agreed PO or supplier terms.Strengthen future PO quality clauses based on identified gaps.

Controlled reduction of incoming inspection. Build reliable supplier QC approval throughdemonstrated process capability, accurate test reports and sustained conformity. Recommend a gradual move from 100 percent incoming inspection to risk-based sampling only after supplierperformance supports it and the change is approved. Retain random verification and restorestricter inspection if defects or report discrepancies recur.

ISO records and continuous improvement. Update relevant ISO quality-system documentation andmaintain supplier audit reports, incoming inspection records, approved specifications anddrawings, NCs, action trackers and effectiveness evidence. Track defect and recurrencetrends, supplier action closure and incoming inspection effort to demonstrate improvedmaterial quality and reduced inspection time.

Required Technical and Professional Skills

• Ability to read electronic schematics, PCB drawings, assembly drawings and wiringdiagrams, and assess electronic manufacturing workmanship.
• Hands-on technical knowledge to assess and verify the work of QC inspectors, supportedby testing ability, structured root-cause analysis and clear technical documentation.
• Ability to coordinate firmly with design, PCB production, assembly, testing and serviceteams, and ensure actions are implemented and sustained.
• Strong ownership, attention to detail and the discipline to keep quality issues visibleuntil verified closure.

Accountability

The Senior QC Engineer is accountable for driving product reliability through effectivequality controls and verified action closure across departments. The role extends beyondidentifying defects: the engineer must ensure that the responsible teams implement therequired improvements and that their effectiveness is demonstrated.