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Quality Audit Software

Quality Audit Software for Consistent Products, Processes and Service

Run product, process, service, packaging, supplier, defect, non-conformance, complaint, and CAPA follow-up audits with verified evidence, consistent scoring, corrective actions, and real-time quality visibility across every location.

Verified quality findingsConsistent audit scoringCAPA and action tracking
Taqtics audit dashboard showing quality audit scores, defect trends, open non-conformances, and corrective actions
Quality Audit Score94%
Locations Audited134
Open Quality Gaps27
Quality Audit Software

A clearer way to verify quality and close recurring gaps

Taqtics connects quality standards, inspection criteria, mobile evidence, scoring, defect records, reports, responsible teams, and corrective actions in one workflow across locations, products, processes, suppliers, departments, and service teams.

Verify quality executionCapture product, batch, process, supplier, location, time, photos, comments, defect details, and supporting evidence together.
Standardize quality scoringApply the same inspection criteria, answer types, severity rules, evidence requirements, category weights, and score logic across teams.
Close defects and quality gapsAssign owners, containment, root-cause follow-up, deadlines, escalation, corrective action, effectiveness checks, and verified closure.
Manual Quality Audit Gaps

Where manual quality audits break down

Select a common gap to see why spreadsheets, paper forms, photo folders, and disconnected CAPA follow-ups make recurring quality issues harder to control.

Defect evidence

Defects are recorded without enough context to investigate them

Teams need the product, batch, process step, supplier, severity, location, photo evidence, comments, containment, owner, and action history behind every quality failure.

Scoring consistency

The same quality condition is judged differently by different auditors

Without clear acceptance criteria, severity definitions, critical checks, and required proof, product and process scores become subjective and hard to compare.

Corrective action

Quality findings stay as audit comments instead of accountable actions

Non-conformances need containment, root-cause notes, ownership, due dates, escalation, closure evidence, and effectiveness verification—not disconnected follow-up messages.

Network visibility

HQ cannot see repeat defects and weak quality areas early enough

Recurring defects, supplier issues, complaint drivers, failed CAPA effectiveness, weak locations, and overdue actions stay hidden without one consolidated view.

Audit Coverage

What a Quality Audit Program Should Cover

Move through five practical quality areas covering product and packaging standards, process execution, service consistency, supplier quality, defects, non-conformance, and CAPA closure.

Coverage area 01

Verify that products and packaging meet approved quality specifications

Compare sampled output against defined appearance, dimensional, finish, condition, packaging, label, batch, and customer-facing standards.

Product Specification ChecksAppearance, dimensions, weight, quantity, finish, freshness, functional condition, batch details, tolerance, sample result, and release status.
Packaging and Label QualityPackaging material, seal integrity, damage, print quality, labels, barcodes, date codes, quantity, presentation, and approved specification match.
Coverage area 02

Verify that approved process controls are followed consistently

Inspect process steps, control points, instructions, sampling methods, approvals, handoffs, deviations, and records that influence final quality.

Process Execution and Control PointsSOP steps, work instructions, sequence, settings, critical process checks, handoffs, approvals, changeovers, and deviation handling.
Inspection and Sampling ControlsSample size, inspection frequency, method, acceptance criteria, pass/fail decisions, rejected units, hold status, and inspector sign-off.
Coverage area 03

Measure service consistency and turn complaints into quality signals

Review service execution, response quality, accuracy, customer experience, complaint handling, recovery, and recurring service failures.

Service Quality ChecksResponse time, staff behaviour, accuracy, service standard, handoff quality, customer-facing execution, issue resolution, and consistency.
Complaint and Recovery ChecksComplaint type, product or service issue, evidence, root cause, refund or replacement, action owner, closure proof, and repeat complaint trends.
Coverage area 04

Control incoming quality and recurring supplier-related defects

Verify supplier documentation, delivered condition, incoming inspection results, certificates, packaging, rejection records, and follow-up actions.

Incoming Quality InspectionMaterial or product condition, quantity, batch, delivery temperature where relevant, packaging integrity, visual defects, specification match, and acceptance status.
Supplier Quality Follow-UpSupplier documents, certificates, rejected items, recurring defects, delivery quality, response time, corrective action, and effectiveness evidence.
Coverage area 05

Track defects and non-conformances from containment to effective closure

Connect defect classification, immediate containment, root cause, responsible teams, corrective action, preventive action, and recurrence checks.

Defect and Non-Conformance ControlDefect type, severity, product, batch, process step, evidence, containment, disposition, investigation, owner, and escalation status.
CAPA and Effectiveness VerificationRoot cause, corrective action, preventive action, deadlines, closure proof, verifier review, recurrence checks, reopening, and effectiveness confirmation.
How It Works

How Taqtics Digitizes Quality Audits

Set quality standards once, schedule audits by location, product, process, supplier, or risk, capture verified findings, score performance consistently, and track every failed check through closure.

01 · ConfigureCreate Quality Audit TemplatesBuild sections for product, packaging, process, service, supplier, complaints, defects, non-conformance, documentation, and CAPA.
02 · StandardizeSet Quality Criteria, Proof, and ScoringDefine Pass, Partial, Fail, and N/A responses, severity, critical checks, specifications, required photos, documents, and score weights.
03 · AssignSchedule by Location, Product, Process, or RiskAssign routine product checks, process audits, supplier reviews, complaint follow-ups, high-defect inspections, or CAPA effectiveness audits.
04 · InspectCapture Verified Quality Findings on MobileRecord product, batch, supplier, defect, severity, process notes, photos, comments, documents, timestamps, location proof, and inspection results.
05 · ImproveAnalyze Defects and Close Corrective ActionsCompare quality scores, identify recurring defects, assign CAPA owners, escalate overdue actions, verify closure, and track effectiveness.
Audit Reliability

Make Every Quality Finding Easier to Trust

Verify the location, inspection time, product or process context, defect evidence, score, severity, ownership, and corrective-action closure behind every quality finding.

Mobile Quality Audit
Facility 218 · Line 03Within Geofence
64%
Today03:18 PM
Quality Score92%
Completion64%
In progress: failed quality checks require evidence
2.0 Product & Packaging Quality5/8 answered
Score: 92%
Progress: 64%Quality: 92%Priority: Critical
Q1*
Critical

Does the sampled product meet the approved specification for appearance, dimensions, finish, and packaging?

PassPartialFailN/A
Defect photo and batch reference required on failure
Q2*

Are packaging seals, labels, date codes, and quantity checks within the approved tolerance?

PassPartialFailN/A
Q3*

Has the detected defect been contained, classified, and assigned for corrective action?

PassPartialFailN/A
Save DraftSubmit
?

Validated observations

Confirm where, when, by whom, and with what product, batch, process, supplier, or defect evidence every response was submitted.

  • Geo-fenced and time-bound location submissions
  • Product, batch, process, supplier, defect, photo, comment, and document evidence
  • Timestamped location-level quality audit trail

Standardized scoring

Apply the same acceptance criteria, objective answer types, category weights, critical-defect rules, proof requirements, and score logic across teams.

  • Question-level quality specifications and inspection instructions
  • Pass, Partial, Fail, and N/A responses with severity and proof rules
  • Automated quality score and category-level summaries

Corrective actions

Assign failed product, process, packaging, service, supplier, complaint, defect, or non-conformance checks and track them through effective closure.

  • Containment, owners, priorities, and deadlines
  • Root-cause notes, escalation, corrective and preventive actions
  • Closure evidence, recurrence checks, and effectiveness verification

Connect audits with corrective action tracking software so quality gaps are not left unresolved.

Quality Audit Programs

Run Different Audits for Different Quality Risks

Quality is not one checklist. Run focused programs to inspect product output, control how quality is produced and delivered, and verify supplier issues, non-conformance, CAPA, and repeat-defect closure.

01
InspectVerify product output and customer-facing quality
Product quality

Product Quality Audits

Specification match, appearance, dimensions, weight, quantity, finish, freshness, condition, batch details, sampling, defects, and release status.

Packaging quality

Packaging Quality Audits

Materials, dimensions, seals, damage, print quality, labels, barcodes, date codes, quantity, case condition, pallet quality, and approved presentation.

02
ControlControl process execution and service consistency
Process quality

Process Quality Audits

SOP execution, control points, process settings, sampling, approvals, handoffs, deviations, records, inspection frequency, and work instructions.

Service quality

Service Quality Audits

Customer experience, accuracy, response time, staff behaviour, service consistency, issue handling, complaint recovery, and recurring service gaps.

03
ImproveControl external defects and verify improvement
Supplier quality

Supplier Quality Audits

Incoming quality, certificates, delivered condition, specification match, rejected items, recurring supplier defects, response time, and corrective follow-up.

Defects and CAPA

Non-Conformance and CAPA Audits

Defect severity, containment, disposition, root cause, corrective action, preventive action, owners, escalation, closure proof, recurrence, and effectiveness checks.

Reports and AI Insights

Quality Audit Reports That Reveal Recurring Defects

Turn quality audit data into clear visibility across locations, products, processes, suppliers, defect categories, complaints, non-conformance, CAPA, action status, and recurring quality patterns.

01Compare quality performance
02Identify recurring defects
03Track CAPA closure
04Find weak locations and suppliers
View all report insights
  • Quality score by location, region, product, process, supplier, and category
  • Product, packaging, service, and process quality trends
  • Defect type, severity, batch, and non-conformance reports
  • Supplier quality and incoming inspection performance
  • Complaint drivers and recurring customer-facing failures
  • Open, overdue, and closed corrective actions
  • CAPA closure and effectiveness verification status
  • AI-based recurring pattern detection from historical quality data
Quality Performance ReportLocation performance, recurring defects, and CAPA trends
Jul 1 – Jul 31, 2026
Export Report
Quality Audit Score94%↑ 4 pts vs previous period
Open Non-Conformances27↓ 6 vs previous period
CAPA Closure Rate87%↑ 9 pts vs previous period
1. Quality Audit Score by LocationLocation-level product, process, service, supplier, and CAPA performance
Score
96%
Location 118
91%
Location 218
82%
Location 306
71%
Location 421
Quality audit scoreNetwork average
2. Quality Score and Open-Defect TrendsWeekly quality performance and unresolved defect count
Trend
100%75%50%25%0%86%88%90%92%94%191613107Jul 1–7Jul 8–14Jul 15–21Jul 22–28Jul 29–31
Quality scoreOpen defects
AI InsightPackaging seal failures are the highest repeat defect across three locations.Review sealing setup, supplier material consistency, operator verification, and recent CAPA effectiveness before the next production cycle.
Priority · High
Checklist Library

Start With a Ready-to-Use Quality Checklist

Use structured templates for product and packaging quality, incoming inspection, process checks, defect capture, customer complaints, evidence requirements, scoring, and corrective-action triggers.

FAQs

Quality Audit Software Questions

What is quality audit software?

Quality audit software helps teams run mobile product, process, service, supplier, packaging, defect, non-conformance, complaint, and CAPA audits with verified evidence, standardized scoring, reports, and corrective actions.

What types of quality audits can Taqtics support?

Teams can configure product quality, packaging quality, process quality, service quality, supplier quality, incoming inspection, defect, non-conformance, complaint, documentation, training, and CAPA effectiveness audits.

Can Taqtics track defects and non-conformance?

Yes. Teams can capture defect type, severity, product, batch, supplier, process step, location, evidence, containment, root cause, ownership, deadlines, action status, and closure proof.

Can failed quality checks create corrective actions?

Yes. Failed product, process, packaging, service, supplier, complaint, or non-conformance checks can create actions with owners, priorities, deadlines, escalations, evidence, and verification requirements.

Can Taqtics support CAPA follow-up and effectiveness checks?

Yes. Teams can track containment, root cause, corrective action, preventive action, owners, due dates, closure proof, recurrence checks, verifier review, and effectiveness confirmation.

Can managers compare quality performance across locations?

Yes. Reports can compare quality scores, defect categories, supplier issues, complaints, non-conformance, CAPA closure, repeat failures, and action performance across locations, regions, products, and processes.

Can Taqtics identify recurring quality problems?

Yes. Historical audit and action data can help teams identify recurring defects, repeat complaint drivers, weak suppliers, repeated failed checks, ineffective CAPA, and locations requiring attention.

Reliable Quality Audits

Make Every Quality Audit Reliable and Actionable

Digitize product, process, service, supplier, packaging, and defect-related quality audits, verify findings with evidence, identify recurring gaps, and close corrective actions faster across every location.