United Kingdom · Compliance Quality Health Safety · Entry Level (0-2 years)

Quality Technician / Associate

Here is the whole job, in plain words. What it is, a real day, what you decide, how you're judged, how people get here and where they go next. Then the part no course gives you: twelve AI tutors who learn your work.

  • Experience bandEntry Level (0-2 years)
  • Direct reportsNo direct reports
  • Reports toQuality Engineer / Specialist
  • UK framework levelUsually someone starting out, or keeping a process running

Also advertised as Junior Quality Assistant · Compliance Support Officer · QMS Administrator · Quality Data Entry Specialist

Built on an analysis of 43,079 real UK job descriptions · grounded in qualifications employers recognise

Start with a free Future Fluency check, tuned to Quality Technician / Associate

Ten quick questions, one per Future Fluency, asked against this role rather than a generic one. About five minutes, and no card.

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1What this role really is

This isn't just about ticking boxes; it's about making sure our products and processes meet the mark every single time. As a Quality Technician, you'll be right there on the front lines, helping us keep our ISO 9001 certification shiny and our customers happy. You'll be the eyes and ears for quality, spotting issues early and making sure everything's documented properly. Honestly, it's a critical role because you're the first line of defence against things going wrong. You'll learn the ropes from experienced folks, getting a proper grounding in how a global quality system actually works in practice.

2What you'd actually use

The tools this job runs on, and how well you'd need to know each one.

ETQ Reliance (or similar QMS)Intermediate

You'll be logging non-conformances, entering inspection data, and managing assigned tasks within workflows. Essentially, you'll be a regular user, navigating the system to do your daily work.

SAP S/4HANA (QM Module - or similar ERP)Basic

You'll use it to look up batch records, material specifications, and inspection lots. It's about understanding where quality data lives in the broader business system.

Minitab (or similar Statistical Analysis Software)Intermediate

You'll use pre-set templates to enter data and run basic statistical tests like control charts or histograms. You'll be following instructions to generate outputs, not designing the analysis.

MS SharePoint/Teams (or similar Collaboration & Document Control)Intermediate

You'll manage documents within established libraries, follow version control procedures, and participate in review/approval workflows. It's about keeping our digital files organised and accessible.

You'll view and interact with pre-built dashboards to monitor daily KPIs, like inspection completion rates. You might export underlying data to Excel for simple tasks, but you won't be building new dashboards.

3What you get to decide, and how that grows

Power in a job isn't your title. It's what you're allowed to decide. Here's how it grows as you move up.

The choiceComing inWhere you are nowThe step above
Product Release/HoldIdentify potential non-conformance and escalate to Quality Engineer. Do NOT make a decision to release or hold product independently.Recommend a product hold based on defined criteria and data. Consult with Quality Engineer for final decision.Authorise product hold based on established procedures and risk assessment. Inform production and sales immediately.
Process Deviation ApprovalReport any observed deviation from a procedure immediately to supervisor. Do NOT approve any deviation.Assess minor, temporary process deviations against risk and documented criteria. Propose temporary approval to Quality Manager.Approve minor, temporary process deviations with documented justification. Escalate major deviations to Director.
CAPA Investigation ScopeAssist in data collection for CAPA investigations as directed. Do NOT define the scope of an investigation.Define the scope for routine CAPA investigations (e.g., specific product line, process step).Define and approve the scope for complex, cross-functional CAPA investigations.
Document Control ChangesPropose minor edits to documents to supervisor. Do NOT make changes to controlled documents.Draft and route minor document changes for approval (e.g., typo correction, clarity improvement).Authorise and implement significant changes to quality documentation (e.g., new SOPs, major revisions).

4How you'll be judged

The scoreboard, honestly: the hard targets, how often each one is actually looked at, and the quiet human signals that never make it onto a dashboard.

Non-Conformance Report (NCR) Data Entry Accuracy
The percentage of NCRs you log into the QMS without errors (e.g., wrong part number, incorrect date, missing details).
Target · 99% accuracy

If you process 100 NCRs in a month, we'd expect no more than one minor data entry mistake. Missing a critical date on an NCR would count as an error.

On-Time Inspection Completion
The percentage of assigned incoming material or in-process inspections completed by their scheduled deadline.
Target · 95% on-time

If you have 20 inspections due this week, you'd need to complete at least 19 of them by the deadline. Missing one means a potential delay in production.

Document Control Adherence
How often you correctly follow the procedures for document version control, archiving, and retrieval within our QMS.
Target · Zero non-conformances in internal audits related to your document control activities

During an internal audit, the auditor finds that all the documents you've filed are the correct version, in the right place, and properly signed off. No 'old' versions are accidentally in use.

Calibration Schedule Compliance (Assistance)
The percentage of calibration activities you assist with that are completed before the equipment's due date.
Target · 98% compliance

If you're helping the Quality Engineer track 50 pieces of equipment due for calibration this month, only one or two can slip past their date. This is about being organised and proactive.

Learning and Application of QMS Procedures
How quickly and effectively you learn and apply our standard operating procedures (SOPs) for quality tasks.
  • You'll be able to perform routine tasks independently after initial training. You'll ask smart questions about 'why' we do things a certain way, not just 'how'. Your Quality Engineer will see you improving and taking on more complex tasks over time.
Proactive Issue Identification
Your ability to spot potential quality issues or deviations during your routine checks and bring them to the attention of the Quality Engineer.
  • You'll flag an unusual reading on a gauge, notice a batch record that looks incomplete, or point out that a process step might have been missed, rather than just blindly signing off. This shows you're actually thinking, not just processing.
Team Collaboration and Communication
How well you work with the immediate quality team and production staff, communicating clearly and professionally.
  • You'll give clear, concise updates on your work. When you find an issue, you'll explain it calmly to the operator. You'll ask for help when you need it, and offer it when you can. People will generally find you easy to work with.
Adherence to Safety Protocols
Consistently following all health and safety guidelines while performing quality checks on the shop floor or in the lab.
  • You'll always wear your PPE (personal protective equipment) correctly. You'll report any safety hazards you spot. Your supervisor won't have to remind you about basic safety rules.

5Would you like it

The honest version. What people enjoy, and what grinds them down.

What people enjoy
Making Things Right

You get a real kick out of finding an error and correcting it, or ensuring a process is followed perfectly. The idea of preventing a mistake before it happens genuinely excites you.

Spotting a missing signature on a batch record that could have caused an audit finding, and getting it rectified before it becomes an issue.

Learning and Development

You're keen to understand the 'why' behind quality standards and processes. You'll actively ask questions, seek feedback, and want to master new skills related to quality management.

Spending extra time understanding the different types of control charts and how they apply to our production data, even if it's not strictly part of your immediate task.

Contributing to a Tangible Product/Service

You like seeing the direct result of your work in a physical product or a well-run operation. Knowing that your efforts contribute to something real and reliable is important to you.

Seeing a product you've helped quality-check leave the warehouse, knowing it meets all the standards and will satisfy the customer.

What frustrates people
  • The 'Quality Police' Stigma: People sometimes see you as a roadblock, not a helper.
  • Repetitive Tasks: A lot of the daily work involves consistent, routine checks and data entry.
  • Resistance to Change: Getting people to adopt new or even existing procedures can be a slow process.
  • The 'Human Error' Blame Game: When something goes wrong, it's often easier for others to blame an individual than to fix a flawed process.
What this role does not give you
  • High-level strategic decision-making (not yet, anyway).
  • A fast-paced, constantly changing project environment (it's more about consistent execution).
  • A role where you're always the 'hero' solving big, glamorous problems (it's more about preventing them).
  • A job where you never have to deal with paperwork (there's quite a bit, actually).

6Who you work with

This role is fundamental to maintaining our operational quality. Your accurate data collection and adherence to procedures directly support our ISO 9001 certification, reduce the risk of product defects, and help us avoid costly reworks or customer returns. Basically, you're helping us keep our promises to our customers and regulators.

Inside the business
  • Quality Engineers
  • Production Supervisors and Operators
  • Warehouse and Logistics Teams
  • Customer Service (for feedback on issues)
Outside the business
  • Suppliers (for incoming material checks)
  • Certification Auditors (indirectly, through documentation)

7What you need before you start

Not a wish list. The things you would be expected to already have.

  • A genuine interest in quality assurance and a desire to learn how quality systems operate.
  • Strong attention to detail – you're the kind of person who notices small errors.
  • Basic computer literacy, including using Microsoft Office (Word, Excel, Outlook).
  • Ability to follow instructions accurately and work methodically.
  • Good written and verbal communication skills in English.
  • A 'can-do' attitude and willingness to ask questions and seek help when needed.

8What to practise next

Where the job is going, and what to do about it starting this week.

Intermediate Statistical Process Control (SPC)

Moving beyond just plotting data, you'll need to start understanding what the charts are telling you. This means interpreting trends and identifying when a process is 'out of control' or needs attention.

Control Limits vs. Specification Limits · Common Cause vs. Special Cause Variation · Basic Chart Interpretation

  • This month: Ask your Quality Engineer to explain recent control charts and what they mean.
  • Month 2: Take an online course on basic SPC principles (e.g., from ASQ or a reputable MOOC provider).
  • Month 3: Practice interpreting historical control charts and try to identify potential issues before reviewing them with a senior colleague.

Quick win: Start asking 'what does this chart tell us?' every time you look at a control chart, rather than just 'is it in spec?'

Enhanced Root Cause Analysis (RCA) Facilitation

You'll move from just gathering data to actually helping to facilitate initial RCA sessions for simpler issues. This means guiding a small group through a structured problem-solving process.

Fishbone (Ishikawa) Diagrams · Problem Statement Definition · Evidence Gathering & Verification

  • This month: Shadow your Quality Engineer during a 5 Whys or Fishbone session. Take notes on how they lead it.
  • Month 2: Read up on different RCA tools and practice drawing a Fishbone diagram for a hypothetical problem.
  • Month 3: Offer to lead a very simple 5 Whys session for a minor, non-critical issue, with your Quality Engineer observing and providing feedback.

Quick win: For any problem you encounter, mentally (or physically) draw a Fishbone diagram to organise your thoughts on potential causes.

9Staying current once you are in

What people here do to keep up
  • Shadowing experienced Quality Engineers and Technicians to learn practical application of QMS.
  • Participating in internal training sessions on specific quality tools or procedures (e.g., measurement techniques, documentation standards).
  • Attending industry webinars or online courses to build your knowledge of quality standards and best practices.
  • Taking advantage of any internal mentorship programmes to get guidance from senior colleagues.

10How the AI economy is changing work like this

Before we ask anything of you, here's what we can already say about AI and work of this kind:

The new skill this role is being asked for: AI-Assisted Data Validation & Review

Our competitors are already using AI to quickly validate incoming quality documents and inspection reports. It's about reducing manual grunt work and speeding up initial checks, letting you focus on the exceptions.

We'll only ever tell you what we can actually back up. No hype, no scare tactics.

Your PlanIllustration

Built for Quality Technician / Associate

2 units that map to this job, from the qualifications that cover it.

  1. Maintaining Quality and Control in Process ManufacturingSIAS · covers 2 of 10 standardsLevel 3
  2. Implementing Quality Control Systems and Procedures in an Engineering EnvironmentETC Awards Limited · covers 1 of 10 standardsLevel 3
These are the real units behind this job, in the order they rank for it. Nothing here is marked done, because this plan has not been started by anyone yet. Yours would fill in as you go.

The rising capability

Zavmo analysis

What's rising in its place

This is where the work is heading, and the higher pay with it. Get fluent here and the shift stops being a threat and starts being your edge.

AI-Assisted Data Validation & Review

Our competitors are already using AI to quickly validate incoming quality documents and inspection reports. It's about reducing manual grunt work and speeding up initial checks, letting you focus on the exceptions.

  • Automated Anomaly Detection
  • Template-Based Extraction
  • Confidence Scoring

Digital Literacy for QMS Optimisation

Our QMS platforms are becoming more sophisticated, and understanding how to get the most out of them isn't just for IT anymore. It's about making your daily tasks smoother and more efficient.

  • Workflow Automation Basics
  • Basic Data Querying
  • User Interface Customisation

What you’ll use

Skills this role draws on

Technical

  • ISO 9001:2015 Interpretation & Application
  • Root Cause Analysis (RCA) Methodologies
  • Corrective and Preventive Action (CAPA) Management
  • Statistical Process Control (SPC)

The pathway

How you actually get there, here

How you become one varies far more by country than what one does. This is the UK route. Most people take one of these ways in; the right one depends on where you're starting from.

  1. 1

    Recent College/Vocational Graduate

    0-1 year of initial experience in a related field (e.g., engineering technician, lab assistant).

    Skills to master

    • Strong foundational understanding of technical principles, ability to follow complex instructions, basic data recording, and a keen eye for detail.

    You're ready to move on when

    • Achieved good grades in technical subjects.
    • Completed relevant practical projects or apprenticeships.
    • Demonstrates a strong desire to learn and apply quality principles.
  2. 2

    Manufacturing/Production Operative looking for a career change

    1-3 years experience on the shop floor.

    Skills to master

    • Deep practical understanding of our production processes, strong work ethic, attention to detail in their current role, and a desire to understand the 'why' behind quality.

    You're ready to move on when

    • Consistently followed procedures in their current role.
    • Proactively identified small issues or areas for improvement.
    • Expressed interest in moving into a quality-focused role.
    • Understands the impact of quality on production efficiency.
  3. 3

    Administrative Assistant with a technical bent

    1-2 years experience in an administrative role, ideally in a technical or regulated environment.

    Skills to master

    • Exceptional organisational skills, meticulous record-keeping, strong written communication, and an aptitude for learning technical concepts.

    You're ready to move on when

    • Managed complex filing systems or databases.
    • Demonstrated high accuracy in administrative tasks.
    • Expressed interest in moving into a more technical or process-driven role.
    • Quickly picks up new software and systems.

11Where this role leads

The long view:Your journey starts here, at the foundational level, but the potential for growth is immense. We're looking for someone who sees this as more than just a job; it's a chance to build a real career in a field that genuinely makes a difference to product safety and customer trust.

Pay & demand

Pay and demand for this role will appear here, each figure traced to a named authoritative source (e.g. the ONS Annual Survey of Hours and Earnings, under the Open Government Licence). We don’t show numbers we can’t attribute.

The ten Future Fluencies

Zavmo analysis

The credential is what you can do today. These are what keep you valuable.

A qualification proves you can do the job as it's defined today. These ten are what decide whether you're still the obvious person for it in five years. They're the capabilities employers are now writing into senior roles faster than people are learning them. Zavmo weaves them through whatever you study, so you come out with both: the credential and the fluency.

The highlighted ones are the Fluencies your role leans on hardest, from how Quality Technician / Associate is actually changing. In about two minutes, the free confidence check asks where you stand on each of the ten. That's the whole check, and it's what makes the plan yours rather than generic.

12The team that's yours

No two people are taught the same way. This is one-to-one, not one-to-many.

Zavmo is a hyper-personalised AI learning platform. Twelve virtual tutors, each with a different way of teaching, and one orchestration agent that picks the right one for the moment. So every single lesson is shaped around you, your role, and the way you learn. Not a course everyone sits through. A conversation built for you, and no one else.

…and nine more, matched to you after your first chat. Meet all twelve

13What it feels like

A conversation, not a course

Because your tutor knows your role, your projects and your last session, learning sounds like this. And it's different for every single person:

Maintaining Quality and Control in Process ManufacturingLevel 3

Applied to your work in Quality Technician / Associate

This unit aims to provide learners with a comprehensive understanding of maintaining quality and control in process manufacturing. Learners will learn about the function and components of process control systems, documentation requirements and control procedures, and the role of laboratory procedures in quality control.

How the thinking builds
  1. Remember
  2. Understand
  3. Apply
  4. Analyse
  5. Evaluate
  6. Create
An illustration of a Zavmo lesson, built from this role’s own route. The unit, its objective and every criterion above are the awarding body’s own words, not an example.

One to one, not one to many

No two people run this the same way

A course is written once and handed to everyone. This is assembled around you, and keeps changing as it learns you. Five things it reads, and what each one changes.

  1. Your actual work Every lesson is taught against a live piece of your own work, not a worked example from a textbook.
  2. What you already know The first conversation finds your starting point, so you skip what you can already do and spend the time on what you cannot.
  3. The conditions you learn under Not a learning-styles quiz. The evidence does not support those. The dimensions the research does back, read once and used to shape the plan.
  4. How far you got last time It picks up mid-thought. The tutor knows what you said, what you struggled with, and what it asked you to try.
  5. Which tutor suits the moment Twelve of them, each for a different kind of thinking. The one who walks you through a first idea is not the one who stress-tests it.

See how you learn, free. Eight questions, no sign-up. A directional taster; the diagnostic inside Zavmo goes deeper and keeps adapting.

DemonstrateIllustration

Evidenced on your work in Quality Technician / Associate

You do not finish by watching something. You finish by showing it on the work you already do, against the measures this job is judged on.

  • Non-Conformance Report (NCR) Data Entry AccuracyThe percentage of NCRs you log into the QMS without errors (e.g., wrong part number, incorrect date, missing details).If you process 100 NCRs in a month, we'd expect no more than one minor data entry mistake. Missing a critical date on an NCR would count as an error.99% accuracy
  • On-Time Inspection CompletionThe percentage of assigned incoming material or in-process inspections completed by their scheduled deadline.If you have 20 inspections due this week, you'd need to complete at least 19 of them by the deadline. Missing one means a potential delay in production.95% on-time
  • Document Control AdherenceHow often you correctly follow the procedures for document version control, archiving, and retrieval within our QMS.During an internal audit, the auditor finds that all the documents you've filed are the correct version, in the right place, and properly signed off. No 'old' versions are accidentally in use.Zero non-conformances in internal audits related to your document control activities
  • Calibration Schedule Compliance (Assistance)The percentage of calibration activities you assist with that are completed before the equipment's due date.If you're helping the Quality Engineer track 50 pieces of equipment due for calibration this month, only one or two can slip past their date. This is about being organised and proactive.98% compliance
These are this job's own measures, with its own targets. Nothing is marked evidenced, because nobody has started this yet. Yours would fill in from the work you bring.

Your passport

This isn't a certificate you file away. It's a passport to the life you're designing.

Every credit you earn and every fluency you build adds up: evidence where it counts, carried with you. Zavmo keeps the map: where you are, where you're heading, and the next step, at your pace, around your life. From Quality Technician / Associate to Quality Engineer / Specialist (Level 002), and whatever you decide comes after.

Level 2 · in progressAI Fluency→ Quality Engineer / Specialist (Level 002)→ your design
Where this takes you

Your journey starts here, at the foundational level, but the potential for growth is immense. We're looking for someone who sees this as more than just a job; it's a chance to build a real career in a field that genuinely makes a difference to product safety and customer trust.

See Your Progress GrowIllustration
Quality Technician / Associate
  • ISO 9001:2015 Interpretation & Application
  • Root Cause Analysis (RCA) Methodologies
  • Corrective and Preventive Action (CAPA) Management
  • Statistical Process Control (SPC)
This is your Mind Palace on learn.zavmo.ai. Every skill above comes from this role's own record, not an example borrowed from another job. A node lights up when you evidence it, and what you build stays yours between jobs. That is the part a course cannot do.

14The detail, folded away

Everything else the record holds

The career branches in full, how AI is already showing up in the day-to-day, and the questions people ask about this job. Here when you want them, out of the way while you decide.

Where it leads next, rung by rung

Where it leads

The career path, and where it branches

Quality Technician / Associate is a start, not a ceiling. Each step below asks for new skills and hands back more autonomy.

  1. Quality Engineer / Specialist (Level 002)

    2-3 years in the Quality Technician role.

    This is the natural next step, moving from executing tasks to owning specific quality processes and contributing to investigations.

    • Leading minor non-conformance investigations.
    • Contributing to internal audits as an auditor.
    • Configuring basic workflows within the QMS.
    • Interpreting SPC charts and recommending actions.
Working with AI on the job

Working with AI

Where AI is starting to help

Imagine spending less time on repetitive data entry and more time actually learning and understanding our quality processes. That's what AI can do for you in this role.

Truth is, a lot of entry-level quality work involves sifting through documents and logging data. AI isn't here to replace you, but to give you a serious leg up, turning those hours of manual grind into minutes of verification. Think of it as your super-efficient digital assistant, helping you get through the necessary admin faster so you can focus on the interesting stuff.

Automated Document Triage & Review

Use AI to scan incoming supplier certificates of analysis, inspection reports, and other quality documents. It'll flag non-conforming data, missing signatures, or deviations from templates, turning a 30-minute manual review into a 5-minute verification. You'll just need to double-check its work.

Smart Data Entry & Logging

Feed structured notes from your inspections or audit findings into an AI tool, and it can help draft the initial entries for NCRs or inspection logs in our QMS. This means less typing and fewer typos, freeing you up to focus on the actual quality issue.

Quick SOP & Procedure Search

Got a question about a specific procedure or standard? Instead of sifting through dozens of documents, use an LLM to quickly find the relevant section, summarise it, or even explain it in simpler terms. It's like having an instant expert on our entire document library.

Basic Report Generation Assistance

When you need to summarise your weekly inspection results or compile data for a monthly quality report, AI can help. Give it your raw data and key points, and it can draft an initial summary or even populate a basic report template, saving you hours of formatting.

Common questions

Common questions

How do you become a Quality Technician / Associate?

Common routes in include Recent College/Vocational Graduate (0-1 year of initial experience in a related field (e.g., engineering technician, lab assistant).), Manufacturing/Production Operative looking for a career change (1-3 years experience on the shop floor.) and Administrative Assistant with a technical bent (1-2 years experience in an administrative role, ideally in a technical or regulated environment.). Times vary with prior experience.

Where can a Quality Technician / Associate progress to?

This role can lead on to Quality Engineer / Specialist (Level 002) (2-3 years in the Quality Technician role.), depending on the skills you build.

What level is a Quality Technician / Associate in the UK?

This role aligns to RQF Level 2 on the UK framework, a guide to the depth of qualification it maps to, not a hard entry bar.

What new skills matter most for a Quality Technician / Associate?

Increasingly, AI-Assisted Data Validation & Review and Digital Literacy for QMS Optimisation. These are the areas where the higher-paid, future-proof work is heading.

The honest bit

You’ve started things before

Most of them were built for a room full of people who aren’t you. A cohort moves on whether or not your week allowed it, and by the third week the thing you’re behind on becomes the reason you stop opening it.

There’s no cohort here, and no timetable to fall behind. Before anything starts, Zavmo asks when you’re sharpest and how long you can realistically sit down for, then builds the sessions around those answers. A bad fortnight changes your pace. It doesn’t put you behind.

And you only pay once you start learning. Searching and planning are free, and you can cancel any time — so the cost of finding out is an afternoon, not a year.

What it costs

Less than one coaching session. Every month.

A single career-coaching hour costs more than a month of this, and it ends when the hour does. Zavmo doesn't. It's £70 a month, about £2.30 a day, for a companion that knows a Quality Technician / Associate, works on the job you actually do, and keeps going at your pace rather than a timetable's.

  • Searching and planning stay free. You only pay when you start learning.
  • Your credits are yours. Regulated, and they don't vanish when a subscription ends.
  • Cancel any time and billing stops. No notice period, no minimum term.

Your path, personalised

You have the map. Walking it is the part we do together.

This route runs to 10 national skill standards. That is a real journey.

Zavmo shapes a learning experience as unique as you are. It fits how you learn, your pace and the work you already do. Every step stays benchmarked to recognised national standards. That’s the plan for becoming a Quality Technician / Associate: personal to you, and it still counts. The first steps are free.

Independent research finds well-designed intelligent tutoring performs nearly as well as one-to-one human tutoring: VanLehn (2011), Educational Psychologist.

A private tutor in the UK averages £35–40 an hour . Zavmo is £70/month.

A real plan on learn.zavmo.ai: Ofqual-regulated units, credits, and a three-month run at your own pace.
Start free No commitment. See your first steps free.

15Where to go from here

Other roles at Level 2

Same depth of qualification, different job. Useful if the work appeals but this particular role does not.

Other roles in Compliance Quality Health Safety

Stay in the field you know and move sideways rather than up.

If you leave this industry

The skills you'll gain in this role – understanding quality systems, process control, auditing, and problem-solving – are highly transferable across almost any regulated industry. Think pharmaceuticals, aerospace, automotive, food & beverage, or medical devices. Once you understand ISO 9001, adapting to other standards is much easier.

Not sure this is the right direction?

Work out what you actually want from work first, then come back and see which roles fit it. Takes about ten minutes.

This role profile is © 2026Growth Engineering Technologies Ltd. Built from UK occupational standards and regulated qualification data, and written for Zavmo.

You're not behind. You're right on time. The shift is only just beginning. Your role won't look the same in two years. Be the one who leads the change, not the one it happens to. Build my plan, free Here's the first ten minutes: a 2-minute confidence check → your personalised roadmap → meet the tutors matched to you. No card, cancel any time. No card. Build your plan, see your roadmap and meet the twelve tutors matched to you. All free. When you're ready to start learning, it's £70 a month, billed monthly. Cancel any time and billing stops.