United Kingdom · Compliance, quality and safety · Mid-Level (2-5 years)

Management Systems Specialist

Here is the whole job, in plain words. What it is, 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.

See how AI is changing this job, and get the full read by email.

As a Management Systems Specialist, a good place to start on AI-Assisted Compliance Analysis is Automating a Repeated Task in Own Work, a free Future Fluency module at Level 3. You'd practise automating the part of a weekly task that never changes, and checking it really saves you time.

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One email: what AI is changing in this job, the new skills it asks for, where it leads, and where to start free. With a link back here. Nothing else follows unless you confirm your address.

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  • Experience bandMid-Level (2-5 years)
  • Direct reportsNo direct reports
  • Reports toManager, Integrated Management Systems
  • UK framework levelUsually a coordinator, or early in a professional job

Also advertised as ISO Systems Coordinator · Compliance Systems Analyst · Quality Assurance Specialist (ISO) · EHSQ Systems Professional

Built on 43,079 real UK job descriptions we analysed · grounded in what real qualifications cover

1From this job to a course

The qualifications matched to this job

GQA PAA\VQ-SET Level 3 Diploma for a Bulk Storage Operator (Technician) GQA Qualifications Limited · Level 3 · covers 2 of 10 standards
IWFM Level 4 Diploma in Facilities Management Practice Institute of Workplace and Facilities Management · Level 4 · covers 1 of 10 standards
ProQual Level 4 NVQ Diploma in Management ProQual Awarding Body · Level 4 · covers 1 of 10 standards
GQA PAA\VQ-SET Level 3 Certificate in Laboratory Technical Skills GQA Qualifications Limited · Level 3 · covers 1 of 10 standards
GQA Level 5 Diploma in the Practice of Process Safety Management GQA Qualifications Limited · Level 5 · covers 1 of 10 standards

Matched from the standards this job is measured against: a suggestion, not an official ruling.

The units you would start with

Comply with External and Internal Obligations within a Bulk Storage Operations Environment GQA PAA\VQ-SET Level 3 Diploma for a Bulk Storage Operator (Technician)
Implement health and safety and environmental facilities management procedures IWFM Level 4 Diploma in Facilities Management Practice
Manage Health and Safety in own area of responsibility ProQual Level 4 NVQ Diploma in Management
Good Manufacturing Practice GQA PAA\VQ-SET Level 3 Certificate in Laboratory Technical Skills
Principles of Safe Manufacture of Quality Medicines in the Pharmaceutical Environment Open Awards Level 3 Technical Occupational Entry in the Principles and Practice for Pharmacy Technicians (Diploma)
Understand how to comply with the relevant Regulations, Industry Standards and Management Requirements for Process Safety GQA Level 5 Diploma in the Practice of Process Safety Management

The future skills this job leans on

AI Fluency working with AI as a thinking partner
Data Fluency turning numbers into a decision
AI Governance Fluency using AI responsibly
Automation Fluency building AI into how work runs
Systems Fluency seeing the whole picture
Your Plan Illustration

Built for Management Systems Specialist

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

  1. Comply with External and Internal Obligations within a Bulk Storage Operations Environment GQA Qualifications Limited · covers 2 of 10 standards Level 3
  2. Implement health and safety and environmental facilities management procedures Institute of Workplace and Facilities Management · covers 1 of 10 standards Level 4
  3. Manage Health and Safety in own area of responsibility ProQual Awarding Body · covers 1 of 10 standards Level 4
  4. Good Manufacturing Practice GQA Qualifications Limited · covers 1 of 10 standards Level 3
  5. Principles of Safe Manufacture of Quality Medicines in the Pharmaceutical Environment Open Awards · covers 1 of 10 standards Level 3
  6. Understand how to comply with the relevant Regulations, Industry Standards and Management Requirements for Process Safety GQA Qualifications Limited · covers 1 of 10 standards Level 5
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.

2AI and this work

Will AI change your work as a Management Systems Specialist?

Nobody can say exactly how. Here is what this job is being asked for next, and where to start.

The new skills this role is being asked for

  • AI-Assisted Compliance Analysis
  • Digital Process Optimisation
Why each one is rising

The future skills this job leans on

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

What happens when you start

Next, a free account. We build your Management Systems Specialist plan as you set up, starting with the free Automation Fluency module. No card.

Your first Future Fluency module is free. After that, your AI tutor is £70 a month.

Keep this read. One email with what AI is changing in this job, the new skills it asks for and where to start free. Nothing else follows unless you confirm your address.

3What this role really is

This job means checking that ISO management systems work in practice. It involves checking processes day to day, spotting issues, and helping teams fix them. The work is about making a business more reliable.

4What you'd actually use

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

EHSQ/GRC Platform (e.g., Intelex, Cority, Enablon) Intermediate

You'll be entering audit findings, updating risk registers, managing CAPA records, and pulling standard reports. You should be comfortable navigating the system and ensuring data accuracy.

SharePoint Online (for Document Control) Intermediate

Uploading documents, managing version control for assigned procedures, and following established review/approval workflows. You'll need to know where everything lives and how to keep it tidy.

Audit Management Software (e.g., AuditBoard, Workiva) Basic

Populating checklists during internal audits, uploading evidence, and responding to findings assigned to you. You'll be a user, not necessarily a configurator.

Power BI / Tableau (for basic reporting) Basic

Viewing and filtering pre-built dashboards to track KPIs for your assigned areas. You might export data for simple analysis, but you won't be building complex dashboards from scratch.

MS Visio / Miro (for process mapping) Intermediate

Creating basic process flowcharts to document current state processes or proposed improvements. You'll use these to visually communicate how things work.

MS Teams (for collaboration) Intermediate

Participating in team channels, managing tasks in Planner, and using it for daily communication and meetings with operational teams.

5What 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 in Where you are nowThe step above
Internal Audit Scope & Schedule Proposes initial scope and schedule; requires full review and approval from supervisor. Defines scope and schedule for assigned audits within the annual plan; consults with manager on significant deviations or complex areas. Approves internal audit schedules for multiple workstreams; consults with Director on strategic audit focus areas.
Corrective Action Plan (CAPA) Approval Drafts CAPA plans; requires full review and approval from supervisor and process owner. Develops and verifies CAPA plans with process owners; manager reviews and approves final plan before closure. Reviews and approves complex or high-impact CAPA plans; provides guidance on systemic corrective actions.
Document Updates (Procedures/Work Instructions) Suggests minor edits to existing documents; changes are implemented by supervisor. Drafts and updates specific procedures or work instructions within their assigned scope; requires approval from process owner and manager. Designs new document structures or major procedure revisions; approves changes for their responsible standards/regions.
Process Improvement Recommendations Identifies potential improvements; escalates to supervisor for further action. Proposes and helps implement process improvements within assigned areas; discusses with manager for resource allocation or cross-functional impact. Leads process re-engineering initiatives; makes recommendations to leadership on significant changes to operational processes.

6How you'll be judged

The scoreboard, and what is not on it. The hard targets, how often each is actually looked at, and the quiet signals that never reach a dashboard.

CAPA Closure Rate & Timeliness
The percentage of Corrective and Preventive Actions (CAPAs) that you're responsible for closing, and how quickly they're completed.
Target · 95% of assigned CAPAs closed within agreed timescales; average closure time of 30 days or less.

If you're assigned 10 CAPAs in a month, you'd need to close 9 or 10 of them on time. For instance, a CAPA raised on 1st March with a 15th April deadline needs to be closed by then.

Internal Audit Completion & Quality
The number of internal audits you complete for your assigned area, and the quality of your findings and reports.
Target · 100% of assigned internal audits completed per the annual plan; less than 5% of your audit findings challenged by management.

You might be assigned to audit the 'Warehouse Operations' and 'Customer Service' departments. We'd expect you to complete these on schedule, with clear, evidence-based findings that stand up to scrutiny.

Document Control Accuracy
Ensuring that the documents and records you manage are accurate, up-to-date, and correctly filed within our document control system.
Target · Zero non-conformances related to document control during internal or external audits for your scope.

If the 'Work Instruction for Product Assembly' falls under your scope, you'd ensure the latest version is always available, approved, and older versions are archived correctly. An auditor checking this wouldn't find any discrepancies.

Non-Conformance Reduction (Assigned Area)
The year-over-year reduction in minor non-conformances identified in the specific operational area you support.
Target · 10-15% reduction in minor non-conformances in your assigned area year-over-year.

If the Production department had 20 minor non-conformances last year, we'd aim for 17 or 18 this year, thanks to your work on root cause analysis and process improvements.

Operational Team Engagement
How well you build relationships with the operational teams you support, making them feel like you're helping them, not just auditing them.
  • Operational managers proactively seek your advice on process changes
  • positive feedback from teams during internal surveys or informal check-ins
  • teams are responsive and cooperative during audits, rather than resistant.
Problem-Solving Effectiveness
Your ability to get to the real root cause of issues and propose practical, lasting solutions, rather than just quick fixes.
  • CAPAs you manage don't see recurrence of the same issue
  • solutions are adopted by the business and lead to demonstrable improvements
  • you're able to clearly articulate the 'why' behind a non-conformance and its fix.
Knowledge Sharing & Mentorship
Your willingness and ability to share your ISO knowledge with colleagues, especially new joiners or those less familiar with the systems.
  • You're seen as a go-to person for ISO questions
  • you offer informal guidance to junior team members
  • you contribute to internal training materials or lunch-and-learn sessions
  • colleagues feel comfortable asking you for help.
Proactive Improvement Identification
Your knack for spotting opportunities to make our systems better, even when there isn't a formal non-conformance.
  • You regularly suggest 'Opportunities for Improvement' (OFIs) that get adopted
  • you propose updates to procedures before an audit flags them
  • you identify potential risks before they become problems.

7Would you like it

Both sides. What people enjoy, and what grinds them down.

What people enjoy
Bringing Order to Chaos

You'll get a genuine kick out of taking a messy, inconsistent process and helping a team standardise it. It's about seeing the tangible improvement in how things run, knowing you've made operations smoother and less prone to error.

You're helping the warehouse team document their goods-in process, moving from informal notes to a clear, step-by-step procedure. You feel satisfied seeing them follow it consistently and reduce receiving errors.

Solving Puzzles & Preventing Problems

You enjoy digging into a problem, finding its root cause, and then putting a fix in place that genuinely prevents it from happening again. It's like being a detective for operational issues.

After a minor quality issue, you lead the root cause analysis, identify a training gap, and then help implement a new training module. You're motivated by the fact that this specific issue won't recur.

Making a Real Impact on Quality & Safety

You're driven by the knowledge that your work directly contributes to making our products better, our environmental footprint smaller, and our workplaces safer. It's about tangible improvements that affect people and the planet.

You help implement a new safety procedure after identifying a recurring hazard. Knowing that your work could prevent an injury is a powerful motivator.

What frustrates people
  • The 'Certificate on the Wall' Mentality: Fighting the perception that our ISO systems are just about passing an annual external audit, rather than continuous business improvement.
  • Audit Fatigue: Pleading with busy operational teams for their time when they feel they're constantly being audited by internal, external, and customer auditors.
  • Shadow Systems: Discovering a critical department is running their entire operation off uncontrolled, un-backed-up Excel spreadsheets instead of the official system you've helped implement.
  • The CAPA Graveyard: Chasing people for weeks or even months to close out corrective actions for issues they've already forgotten about.
  • Translating 'Clause 8.3.2' into Business Impact: The endless challenge of explaining the tangible, bottom-line importance of an abstract clause in an ISO standard to a skeptical colleague.
What this role does not give you
  • Direct people management responsibilities (not at this level, anyway).
  • A purely strategic, 'big picture' focus – you'll be very hands-on.
  • A role where you can avoid confrontation or difficult conversations.
  • A 'set it and forget it' type of job; it's all about continuous improvement and ongoing engagement.

8Who you work with

This role is critical for maintaining our certifications, which are often a prerequisite for doing business with key clients. You'll directly contribute to reducing operational risks, improving product/service quality, and ensuring a safe working environment. Your work helps us avoid fines, reputational damage, and operational downtime. Essentially, you're a guardian of our operational integrity.

Inside the business
  • Site Operations Managers (e.g., Manufacturing, Logistics)
  • Quality Control Teams
  • Environmental & Health and Safety Leads
  • Internal Audit Team
  • Document Control Administrator
Outside the business
  • Certification Body (e.g., BSI, SGS)
  • External Auditors
  • Suppliers (for audit purposes)
  • Customers (for specific compliance requests)

9What you need before you start

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

  • At least 2 years of hands-on experience working with ISO management systems (e.g., 9001, 14001, 45001) in an operational or quality role, or equivalent experience.
  • Proven ability to conduct internal audits, including planning, execution, and reporting, and manage corrective actions.
  • Demonstrable experience in drafting or updating operational procedures and work instructions.
  • Strong understanding of root cause analysis methodologies and their practical application.
  • Comfortable using digital tools for document control, task management, and basic reporting (e.g., SharePoint, EHSQ platforms, Excel).
  • Excellent communication skills, both written and verbal, for engaging with diverse teams.
  • A genuine curiosity about how things work and a desire to make them better.

10What to practise next

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

Advanced EHSQ/GRC Platform Configuration

As we rely more heavily on our central EHSQ/GRC platform, the ability to configure workflows, design custom dashboards, and manage user permissions will become essential for driving efficiency and tailored reporting.

Workflow Design & Optimisation · Custom Reporting & Dashboard Creation · User Access & Permissions Management · Data Model Understanding

  • This month: Spend dedicated time exploring the configuration settings and options within our EHSQ/GRC platform.
  • Next quarter: Seek out and complete any vendor-provided training modules or certifications for advanced platform usage.
  • Month 4-6: Work with a more senior colleague to shadow them as they configure a new workflow or build a custom report.
  • Month 6-9: Take on a small project to configure a new feature or optimise an existing workflow within the platform for your assigned area.

Quick win: Identify one report you regularly pull manually and explore if it can be automated or customised within the EHSQ/GRC platform's reporting module.

Advanced Data Visualisation (Power BI/Tableau)

Moving beyond just viewing dashboards, you'll need to be able to connect to various data sources (including our EHSQ platform's API), build interactive dashboards for Management Review, and use more advanced features to present compelling compliance insights.

Data Source Connection & Transformation · DAX/Calculated Fields · Interactive Dashboard Design · Storytelling with Data

  • This month: Complete an online introductory course on Power BI or Tableau (if you haven't already).
  • Next quarter: Replicate one of our existing compliance dashboards from scratch, connecting to the raw data sources.
  • Month 4-6: Work on a small project to create a new, interactive dashboard for a specific compliance metric (e.g., CAPA closure rates by department).
  • Month 6-9: Present your new dashboard to a small group of stakeholders and gather feedback for iterative improvements.

Quick win: Take a simple compliance dataset (e.g., internal audit findings) and try to visualise it in a new way using Power BI or Tableau, even if it's just a basic chart.

11Staying current once you are in

What people here do to keep up
  • Regularly review updates to ISO standards and relevant legislation to stay current.
  • Attend industry webinars or workshops on specific compliance challenges or new technologies.
  • Participate in internal training sessions on new systems or processes.
  • Seek out mentorship from more senior colleagues in the Compliance team.
  • Join professional bodies like the CQI (Chartered Quality Institute) or IEMA (Institute of Environmental Management and Assessment) for networking and continuous learning.

12The rising capability

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 Compliance Analysis

AI is rapidly changing how we can analyse large datasets of audit findings, incident reports, and CAPAs. Those who can use AI to spot trends and systemic issues faster will be far more effective at preventing problems and driving targeted improvements.

  • Prompt Engineering for Compliance
  • Data Synthesis & Pattern Recognition
  • Impact Analysis Automation
  • AI Output Validation

Digital Process Optimisation

As more of our systems become digital, understanding how to optimise processes within digital platforms (like our EHSQ/GRC system or SharePoint workflows) will be key. It's about moving beyond paper-based thinking to truly digital efficiency.

  • Workflow Automation Principles
  • Data Structure & Integrity
  • User Experience (UX) for Compliance Tools
  • Integration Basics

13What you’ll use

What you’ll use

Skills this role draws on

Technical

  • Integrated Management Systems (IMS) Concepts
  • PDCA (Plan-Do-Check-Act) Cycle Application
  • Root Cause Analysis (RCA) Techniques
  • Risk-Based Thinking & Auditing
  • Process Mapping & Documentation (BPMN basics)
  • ISO 19011 Auditing Guidelines

14The pathway

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

    ISO Coordinator / Quality Assistant

    1-2 years

    Skills to master

    • Document control, basic internal auditing, CAPA follow-up, understanding of core ISO clauses, data entry into EHSQ systems.

    You're ready to move on when

    • Consistently completes assigned tasks accurately and on time.
    • Demonstrates initiative in learning about ISO standards.
    • Can independently manage simple non-conformances from start to finish.
    • Receives positive feedback on attention to detail and reliability.
  2. 2

    Operational Role with Compliance Exposure (e.g., Production Supervisor, EHS Officer)

    2-3 years

    Skills to master

    • Practical application of ISO requirements in an operational setting, understanding of process interdependencies, experience with incident investigation, basic risk assessment.

    You're ready to move on when

    • Proactively identifies and addresses compliance issues within their operational area.
    • Has a strong understanding of how operational processes interact with ISO requirements.
    • Demonstrates a keen interest in improving systems and preventing recurrence.
    • Can clearly articulate the business impact of compliance failures.
  3. 3

    Junior Compliance Analyst / Auditor

    1-2 years

    Skills to master

    • Audit methodology, regulatory research, data analysis for compliance, stakeholder engagement, report writing.

    You're ready to move on when

    • Has experience conducting formal audits (internal or external).
    • Can interpret regulatory requirements and apply them to business processes.
    • Strong analytical skills and ability to present findings clearly.
    • Comfortable interacting with various levels of management.

15Where this role leads

The long view: This work can lead to designing management systems across a whole standard or region, managing an integrated management system, or specialising in compliance and quality data analysis.

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 Management Systems Specialist is actually changing.

How you would learn this

One to one, on the work you already do

A tutor sets the task against your own job and marks the reasoning, at your pace. There is no cohort to fall behind.

A lesson from Comply with External and Internal Obligations within a Bulk Storage Operations Environment, worked against Management Systems Specialist.

Comply with External and Internal Obligations within a Bulk Storage Operations Environment Level 3

Applied to your work in Management Systems Specialist

The objective of this unit is to enable learners to comply with both external and internal obligations within a bulk storage operations environment. Learners will be able to perform audits, inspections, and safety sampling, adhere to safe systems of work, control systems for fiscal and excise compliance, and review and improve standard operating procedures.

How the thinking builds
  1. 1 Remember
  2. 2 Understand
  3. 3 Apply
  4. 4 Analyse
  5. 5 Evaluate
  6. 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.

It is £70 a month, billed monthly. Your free first module is Future Fluency, and you can cancel any time.

See Your Progress Grow Illustration
Management Systems Specialist
  • Integrated Management Systems (IMS) Concepts
  • PDCA (Plan-Do-Check-Act) Cycle Application
  • Root Cause Analysis (RCA) Techniques
  • Risk-Based Thinking & Auditing
  • Process Mapping & Documentation (BPMN basics)
  • ISO 19011 Auditing Guidelines
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.

16The 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

Management Systems Specialist is a start, not a ceiling. Each step below asks for new skills and hands back more autonomy.

  1. Senior Management Systems Specialist (L3)

    3-5 years in current role

    You'll move from owning specific processes or sites to leading audit teams, mentoring junior specialists, and managing projects like implementing a new ISO standard across multiple departments. You'll be making more independent technical decisions.

    • Advanced Lead Auditor techniques (e.g., ISO 19011 application).
    • Broader understanding of multiple ISO standards and their integration.
    • More in-depth root cause analysis methodologies (e.g., FMEA basics).
    • Ability to design and implement new procedures, not just update existing ones.
Working with AI on the job

Working with AI

Where AI is starting to help

Imagine spending less time on the tedious bits of compliance and more time on the strategic stuff that truly improves our systems. AI isn't here to replace you; it's here to supercharge your productivity and help you focus on what really matters.

Our department is investing in AI tools to streamline how we manage ISO systems. For a Management Systems Specialist, this means automating some of the repetitive tasks, getting smarter insights, and making your day-to-day work more efficient and impactful. You'll be at the forefront of using these tools to transform our compliance efforts.

Automated Audit Report Generation

AI can draft the initial audit report by pulling together your checklist responses, uploaded photo evidence, and interview notes. It'll even flag inconsistencies and suggest potential non-conformance wording based on the standard's clauses, giving you a solid first draft in minutes. You'll then refine it, adding your expert judgment.

Systemic Root Cause Analysis Assistant

Instead of manually sifting through old records, AI can analyse thousands of historical CAPA and NCR records. It'll identify recurring themes, hidden correlations, and systemic risks across different sites or departments that might be invisible to human analysis. This helps you target your improvement efforts where they'll have the biggest impact.

Regulatory & Standard Change Monitoring

An AI agent continuously scans ISO publications and regulatory bodies for updates. It provides you with a summarised brief of changes and performs an initial impact analysis against our current internal procedures, flagging documents that likely need your review. No more manual trawling through dense publications!

Compliance Communication Simplifier

Use AI tools to translate dense, jargon-filled ISO clauses and internal procedures into simple, easy-to-understand language for frontline employee training, toolbox talks, and company-wide communications. It can even help generate simple visual aids or infographics to make complex topics more digestible.

Common questions

Common questions

How do you become a Management Systems Specialist?

Common routes in include ISO Coordinator / Quality Assistant (1-2 years), Operational Role with Compliance Exposure (e.g., Production Supervisor, EHS Officer) (2-3 years) and Junior Compliance Analyst / Auditor (1-2 years). Times vary with prior experience.

Where can a Management Systems Specialist progress to?

This role can lead on to Senior Management Systems Specialist (3-5 years in current role), depending on the skills you build.

What new skills matter most for a Management Systems Specialist?

Increasingly, AI-Assisted Compliance Analysis and Digital Process Optimisation. These are the skills our record of this role lists as growing.

Free tools

Want a read on where you stand?

Three free tools, no account needed. Each one ends with a role, a level and a way in.

17Where to go from here

Other roles at Level 3

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

More jobs in compliance, quality and safety

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

If you leave this industry

The skills built in this role apply across most industries that work to ISO standards, from manufacturing and aerospace to healthcare and technology. Process, quality and risk management skills carry over between sectors.

This role profile is © 2026 Growth 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. Start my free Automation Fluency module What happens next: a free account, then we build your plan as you set up. 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.