UK

United Kingdom · Operations · Director/VP (16-20 years)

Director, Global Quality Systems

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  • Experience bandDirector/VP (16-20 years)
  • Direct reports25-100+ reports
  • Reports toVP, Global Quality & Compliance
  • UK framework levelUsually a director, accountable for a division and its numbers

Also advertised as Head of Operations Quality Systems · Global QMS Lead · VP of Quality Systems (smaller firm equivalent)

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

Two short quizzes about you

1From this job to a course

The qualifications matched to this job

GQA Level 5 Diploma in the Practice of Process Safety Management GQA Qualifications Limited · Level 5 · covers 3 of 17 standards
ProQual Level 6 NVQ Diploma in Quality Management ProQual Awarding Body · Level 6 · covers 1 of 17 standards
IAO Level 5 Diploma in Leadership and Management Innovate Awarding · Level 5 · covers 1 of 17 standards
GQA PAA\VQ-SET Level 3 Diploma for a Bulk Storage Operator (Technician) GQA Qualifications Limited · Level 3 · covers 1 of 17 standards
GQA PAA\VQ-SET Level 3 Certificate in Laboratory Technical Skills GQA Qualifications Limited · Level 3 · covers 1 of 17 standards

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

The units you would start with

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
Quality Management Systems and Standards ProQual Level 6 NVQ Diploma in Quality Management
Managing quality and quality systems IAO Level 5 Diploma in Leadership and Management
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)
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)
Good Manufacturing Practice GQA PAA\VQ-SET Level 3 Certificate in Laboratory Technical Skills

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
Change Fluency taking people through change
Your Plan Illustration

Built for Director, Global Quality Systems

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

  1. Understand how to comply with the relevant Regulations, Industry Standards and Management Requirements for Process Safety GQA Qualifications Limited · covers 3 of 17 standards Level 5
  2. Quality Management Systems and Standards ProQual Awarding Body · covers 1 of 17 standards Level 6
  3. Managing quality and quality systems Innovate Awarding · covers 1 of 17 standards Level 5
  4. Principles of Safe Manufacture of Quality Medicines in the Pharmaceutical Environment Open Awards · covers 3 of 17 standards Level 3
  5. Comply with External and Internal Obligations within a Bulk Storage Operations Environment GQA Qualifications Limited · covers 1 of 17 standards Level 3
  6. Good Manufacturing Practice GQA Qualifications Limited · covers 1 of 17 standards Level 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.

2AI and this work

Will AI change your work as a Director, Global Quality Systems?

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 & Machine Learning for Predictive Quality
  • Digital Transformation Leadership for Operations
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 Director, Global Quality Systems 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.

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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 role leads the strategy for how global quality systems are managed across an organisation. It covers compliance, efficiency, and readiness for regulatory scrutiny, and involves leading a team responsible for product integrity.

4What you'd actually use

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

Veeva Vault QMS / MasterControl / TrackWise Digital / ETQ Reliance (eQMS) Strategic/Architect

Leading platform selection decisions, defining global system architecture, owning the Validation Master Plan (VMP), and setting the strategic roadmap for eQMS evolution. You're not configuring it daily, but you're dictating how it's configured and used globally.

SAP S/4HANA (QM Module) / Oracle NetSuite (ERP) Advanced

Designing and approving the integration strategy between the ERP and eQMS, ensuring seamless data flow for quality metrics (e.g., batch records, material specifications) across the enterprise. You'll troubleshoot high-level integration issues and ensure data integrity between systems.

Minitab / JMP (Statistical Software) Advanced

Setting the corporate standard for statistical process control (SPC) and data analysis tools. You'll defend statistical rationale to auditors and guide your team on advanced root cause analysis (e.g., Gage R&R, DOE) and data validation methodologies.

Power BI Premium / Tableau (BI & Reporting) Expert

Owning the executive-level Global Quality dashboard, presenting quality trends, forecasts, and strategic insights to the leadership team and board. You'll oversee the development of complex data models that pull from various quality systems to provide a single source of truth.

SharePoint / MS Project / Jira (Collaboration & Project Management) Expert

Governing the entire information architecture for Quality, including document repositories and collaboration spaces. You'll use MS Project or Jira to manage large-scale, multi-year system implementation and upgrade projects across global teams.

LabWare LIMS / Thermo Fisher SampleManager (LIMS) Advanced

Overseeing the integration and data flow between LIMS and the central eQMS/ERP, ensuring robust data integrity for lab results, sample management, and out-of-specification (OOS) investigations. You'll ensure the LIMS strategy aligns with the broader quality systems vision.

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
Global QMS Platform Selection No involvement. Follows existing system. Provides user feedback on current system's usability. Researches and recommends specific modules or features for existing platform.
Major Regulatory Audit Response Strategy Retrieves specific documents as requested by senior staff. Helps compile audit responses based on established templates. Drafts sections of audit responses, clarifies system functionality for auditors.
Annual Quality Systems Budget Allocation No involvement. Identifies minor software/hardware needs for their workstation. Proposes budget for specific system enhancements or tools within their workstream (e.g., a new Minitab licence).

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.

External Audit Findings (System-Related)
Number of critical or major findings from external regulatory audits directly attributable to quality system deficiencies or data integrity issues.
Target · Zero critical findings; less than 2 major findings annually.

After an FDA inspection at our Cork plant, we had zero critical findings related to QMS data integrity, which is a massive win and directly reflects your team's robust system validation and governance.

Operational Efficiency Gain (Quality Processes)
Percentage reduction in manual steps or cycle time for key quality processes (e.g., CAPA closure, document approval, training assignment) driven by system improvements or automation.
Target · Achieve >20% reduction in manual effort for two critical quality processes per year.

By optimising the change control workflow in Veeva, your team reduced the average approval cycle time by 25%, freeing up 150 hours of managerial time monthly across the organisation.

Cost of Poor Quality (COPQ) Reduction (System-Driven)
Contribution to the overall reduction in COPQ (e.g., scrap, rework, recall costs) through better data visibility, predictive analytics, and proactive controls enabled by the quality systems.
Target · Contribute to a 5% reduction in COPQ related to system-preventable issues annually.

The predictive trend analysis dashboard you championed in Power BI helped us spot an emerging raw material issue early, preventing a potential £1.2M batch recall in Q2.

Global System Uptime & Performance
Maintaining the availability and responsiveness of all critical quality systems (eQMS, LIMS, ERP QM) across all global sites.
Target · 99.9% uptime for all Tier 1 quality systems; average response time <2 seconds.

Despite a major server upgrade, our global Veeva Vault QMS remained available 99.95% of the time last quarter, ensuring no disruption to critical production processes.

Strategic Influence & Thought Leadership
How effectively you shape the company's long-term quality systems roadmap, influence executive decisions, and represent the organisation externally on quality systems best practices.
  • You're regularly invited to C-suite strategy sessions, your input is sought on major IT investments, and you're presenting at industry conferences on quality systems. People listen when you speak about compliance and technology.
Regulatory Relationship Management
Building and maintaining credible, transparent relationships with regulatory bodies, ensuring proactive communication and effective defence of our quality systems during inspections.
  • Regulators view you as a trusted counterpart, and you can navigate complex requests during an audit with calm authority. You're seen as the 'face' of our QMS during high-stakes interactions.
Team Leadership & Capability Building
Your ability to recruit, develop, and retain a high-performing global team of quality systems professionals, fostering a culture of excellence, compliance, and continuous improvement.
  • Your direct reports are progressing in their careers, your team has a low attrition rate, and they're consistently delivering high-quality work. You're known for developing future leaders.
Cross-Functional Collaboration & Alignment
How well you get different departments—like IT, Manufacturing, R&D, and Regulatory—to work together on quality system initiatives, ensuring everyone's on the same page and pulling in the same direction.
  • Major system integration projects are delivered smoothly, with minimal inter-departmental friction. People across the business see you as a partner, not just a 'compliance gatekeeper'.

7Would you like it

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

What people enjoy
Driving Enterprise-Wide Impact

You'll spend your days shaping the global quality strategy, seeing your decisions ripple across all our manufacturing sites and product lines. This isn't about small fixes; it's about significant, company-wide transformation.

Leading the selection and implementation of a new global eQMS that standardises quality processes across 10 countries, directly improving compliance and efficiency for thousands of employees.

Ensuring Regulatory Excellence

You'll be the ultimate guardian of our regulatory standing, constantly thinking about how our systems can meet and exceed GxP requirements. The challenge of keeping us audit-ready, always, is what gets you up in the morning.

Successfully guiding the company through a challenging FDA inspection with zero critical findings, knowing your system architecture and validation efforts were key to that success.

Building High-Performing Teams & Capabilities

A significant part of your role is mentoring and developing your leadership team, empowering them to build strong regional quality systems functions. You thrive on seeing your team members grow and excel.

Developing a global training programme for quality systems managers that significantly upskills the entire team, leading to improved project delivery and higher employee engagement.

What frustrates people
  • Slow organisational adoption of new systems or processes, despite clear benefits and regulatory mandates.
  • The constant tension between business agility and strict GxP compliance, often requiring you to be the 'bad cop'.
  • Managing complex, multi-vendor system integrations that inevitably hit snags and require significant troubleshooting.
  • Justifying large capital expenditures for quality system upgrades to leadership who might not fully grasp the regulatory imperative.
  • Dealing with 'audit fatigue' from your teams, even though you know it's crucial for our business.
  • The political dance required to get different global sites and business units to standardise on a single quality system approach.
What this role does not give you
  • A purely technical, hands-on coding or configuration role – you'll be leading, strategising, and governing.
  • A predictable, unchanging environment – regulatory landscapes shift, technology evolves, and business needs are always changing.
  • Isolation – you'll be constantly interacting with people at all levels, both internally and externally.
  • Instant gratification – large-scale system transformations take years, not months, to fully realise their benefits.

8Who you work with

Your decisions here directly shape the company's global quality posture and regulatory risk profile. You're not just improving a process; you're driving enterprise-level transformation, influencing how we operate, innovate, and compete in highly regulated markets. Get it right, and you're a strategic enabler; get it wrong, and you're a significant business liability.

Inside the business
  • C-Suite (CEO, COO, CTO)
  • Global Head of Manufacturing
  • Head of Regulatory Affairs
  • IT Leadership (CIO, Head of Enterprise Applications)
  • Legal and Compliance Teams
  • Regional Operations Directors
Outside the business
  • Regulatory Bodies (e.g., FDA, EMA, MHRA)
  • External Auditors (ISO, certification bodies)
  • Key Technology Vendors (eQMS providers, ERP vendors)
  • Industry Consortia and Standards Bodies

9What you need before you start

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

  • Extensive experience (10+ years) leading Quality Systems functions or major QMS implementation projects in a highly regulated industry (e.g., Pharma, Biotech, Medical Device).
  • Demonstrable track record of successfully managing large teams (10+ people, including managers) and multi-million-pound budgets.
  • Proven ability to interact and influence at the C-suite level, presenting complex technical and regulatory information clearly and concisely.
  • Deep, practical experience with at least two major eQMS platforms (e.g., Veeva, MasterControl, TrackWise, ETQ Reliance), including full lifecycle implementation and validation.
  • A comprehensive understanding of global GxP regulations and data integrity requirements, with experience defending systems during major regulatory audits.
  • Strong project and programme management skills, capable of overseeing multiple complex system initiatives simultaneously.

10What to practise next

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

Advanced Data Governance for Quality

With more data coming from more sources, ensuring its integrity, quality, and compliance becomes exponentially harder. You'll need to establish enterprise-wide data governance frameworks specifically for quality data, covering everything from data capture to archival.

Data Lineage & Traceability · Data Quality Management Frameworks · Master Data Management (MDM) for Quality

  • This week: Review our current data governance policies. Where are the gaps for quality data?
  • This month: Initiate a working group with IT and data owners to develop a unified data glossary for quality terms.
  • Month 2: Develop a proposal for a dedicated 'Quality Data Steward' role within your team or IT.
  • Month 3: Implement a pilot project to improve data quality for one critical quality attribute.

Quick win: Standardise naming conventions for all new data fields in the eQMS, starting with a small, manageable project.

11Staying current once you are in

What people here do to keep up
  • Regularly attend industry conferences (e.g., ISPE, PDA, RAPS) focused on GxP, quality systems, and digital transformation in regulated industries. You need to stay on top of emerging trends.
  • Actively participate in industry working groups or consortia that are shaping future regulatory guidance for computerised systems. Be a part of the conversation.
  • Pursue executive education programmes in leadership, change management, or digital strategy. This role is as much about people and business as it is about systems.
  • Mentor junior and mid-level quality professionals, sharing your knowledge and building the next generation of leaders. It's a great way to solidify your own understanding too.

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 & Machine Learning for Predictive Quality

Competitors are already using AI to predict quality deviations before they happen, identify root causes faster, and optimise processes. This isn't just about reporting historical data; it's about using advanced analytics to prevent issues and drive proactive quality management. Regulators are also starting to look at how AI is being used in GxP environments.

  • Predictive Modelling for Process Control
  • Natural Language Processing (NLP) for Quality Event Analysis
  • AI Model Validation in GxP
  • Explainable AI (XAI) for Regulatory Scrutiny

Digital Transformation Leadership for Operations

Quality systems aren't isolated; they're part of a broader digital ecosystem. As operations become more digitalised, you need to lead the integration of quality systems into this larger framework, ensuring seamless data flow and process harmonisation across manufacturing, supply chain, and R&D. This means thinking beyond just the QMS.

  • Industry 4.0 & Pharma 4.0 Principles
  • Enterprise Architecture for Quality
  • Data Orchestration & Integration Strategies
  • Cybersecurity & OT Security for GxP

13What you’ll use

What you’ll use

Skills this role draws on

Technical

  • Global GxP / GMP Compliance (Strategic)
  • Enterprise CAPA Process Management & Optimisation
  • Computer System Validation (CSV) & GAMP 5
  • Global Document Control & Records Management Architecture
  • Strategic Audit Management & Regulatory Defence

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

    Senior Manager, Global Quality Systems (Internal Promotion)

    3-5 years in previous role

    Skills to master

    • Deepen your understanding of global regulatory nuances, take on more strategic budget responsibility, lead larger cross-functional projects, and develop your executive communication skills.

    You're ready to move on when

    • Successfully led at least two major global system implementation projects end-to-end.
    • Consistently delivered on strategic objectives, demonstrating strong business acumen.
    • Built and managed a high-performing team of managers, with strong feedback on your leadership style.
    • Acted as the primary point of contact for quality systems during significant external audits.
  2. 2

    Head of Quality Systems (Smaller Company / Scale-up)

    5-8 years in previous role

    Skills to master

    • Gain broader experience across all quality system domains, manage a full departmental budget, build a team from scratch, and develop a more entrepreneurial mindset to navigate resource constraints.

    You're ready to move on when

    • Owned the entire QMS roadmap and budget for a smaller organisation.
    • Successfully scaled quality systems to support rapid company growth.
    • Demonstrated ability to influence and lead without extensive formal authority.
    • Managed all aspects of regulatory compliance related to quality systems.
  3. 3

    Director of IT Quality & Compliance (Cross-Functional Move)

    4-6 years in previous role

    Skills to master

    • Develop a deeper understanding of enterprise IT architecture, cybersecurity, and broader IT compliance frameworks. Learn to bridge the gap between pure IT and quality functions.

    You're ready to move on when

    • Successfully led IT projects with significant GxP impact.
    • Demonstrated strong collaboration with Quality leadership in previous roles.
    • Possesses a strong understanding of both IT infrastructure and quality regulations.
    • Proven ability to manage complex cross-functional relationships and drive alignment.

15Where this role leads

The long view: This work can lead to roles such as Chief Operations Officer or Chief Quality Officer, shaping quality strategy and operations at a senior level.

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 Director, Global Quality Systems is actually changing.

Where it leads

Roles this leads to

Also named as a next step, with no page in the catalogue yet:

  • Head of Operations (Regional / Business Unit)

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 Understand how to comply with the relevant Regulations, Industry Standards and Management Requirements for Process Safety, worked against Director, Global Quality Systems.

Understand how to comply with the relevant Regulations, Industry Standards and Management Requirements for Process Safety Level 5

Applied to your work in Director, Global Quality Systems

The objective of this unit is to provide learners with a comprehensive understanding of the regulations, industry standards, and management requirements for process safety. Learners will understand the role of the Process Safety Leadership Group, relevant frameworks, legal duties, and the role of the Competent Authority.

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
Director, Global Quality Systems
  • Global GxP / GMP Compliance (Strategic)
  • Enterprise CAPA Process Management & Optimisation
  • Computer System Validation (CSV) & GAMP 5
  • Global Document Control & Records Management Architecture
  • Strategic Audit Management & Regulatory Defence
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

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

  1. VP, Global Quality & Compliance

    3-5 years in Director role

    Level 7 (C-Suite)

    • Advanced Risk Management (Enterprise Level) Identifying and mitigating quality risks that could impact the entire company.
    • Global Supply Chain Quality Strategy Defining quality requirements and oversight for the entire supply chain.
    • Product Lifecycle Quality Ownership Ensuring quality from R&D through to commercialisation and post-market surveillance.

  2. Head of Operations (Regional / Business Unit)

    4-6 years in Director role

    Level 6/7 (Director/C-Suite)

    • Operational Excellence (Lean/Six Sigma at scale) Driving continuous improvement across all operational functions.
    • Capacity Planning & Demand Forecasting Managing production schedules and resource allocation.
    • Global Logistics & Distribution Overseeing the movement of goods worldwide.
    • Safety, Health & Environment (SHE) Leadership Ensuring operational compliance with all SHE regulations.
Working with AI on the job

Working with AI

Where AI is starting to help

Let's be real, as a Director, your time is precious. You should be strategising, leading, and engaging with stakeholders, not getting bogged down in manual tasks or sifting through mountains of data. AI isn't here to replace you; it's here to give you back your most valuable asset: time.

In Operations, especially in Quality Systems, there's a huge amount of data and process that AI can handle. Imagine having an intelligent assistant that helps you spot risks, draft critical documents, and even manage regulatory intelligence. That's not science fiction; it's happening now, and it's how you'll elevate your impact.

CAPA Triage & Categorization Oversight

AI can analyse incoming deviation and non-conformance reports, suggesting initial classifications (major/minor) and even identifying potential systemic issues. For you, this means quickly reviewing AI-pre-screened reports, allowing you to allocate investigation resources more strategically and proactively address emerging risks, rather than getting lost in individual incidents.

Predictive Quality Trend Analysis

Imagine AI continuously scanning all quality event data—complaints, deviations, non-conformances—to identify subtle, emerging trends that a human might miss. This isn't just reporting; it's foresight. You'll get early warnings of potential systemic issues, allowing you to initiate preventative actions and allocate resources before they escalate into major, costly problems.

Regulatory Intelligence Assistant

Keeping up with global regulatory updates (FDA, EMA, MHRA, ISO) is a full-time job in itself. AI can monitor these changes, summarise the key impacts on GxP or ISO standards, and even highlight which of our internal SOPs or system configurations might be affected. This drastically cuts down research time for your team, letting you focus on strategic adaptation, not just information gathering.

Audit Response Drafter & Reviewer

When an audit finding is issued, AI can generate a robust first draft of the formal response by pulling relevant data, procedures, and CAPA records from the QMS. For you, this means reviewing a well-structured, comprehensive draft, ensuring all required elements are included and the tone is appropriate, significantly accelerating a high-pressure, time-consuming task.

Common questions

Common questions

How do you become a Director, Global Quality Systems?

Common routes in include Senior Manager, Global Quality Systems (Internal Promotion) (3-5 years in previous role), Head of Quality Systems (Smaller Company / Scale-up) (5-8 years in previous role) and Director of IT Quality & Compliance (Cross-Functional Move) (4-6 years in previous role). Times vary with prior experience.

Where can a Director, Global Quality Systems progress to?

This role can lead on to VP, Global Quality & Compliance (3-5 years in Director role) and Head of Operations (Regional / Business Unit) (4-6 years in Director role), depending on the skills you build.

What new skills matter most for a Director, Global Quality Systems?

Increasingly, AI & Machine Learning for Predictive Quality and Digital Transformation Leadership for Operations. These are the skills our record of this role lists as growing.

Free tools

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

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17Where to go from here

Other roles at Level 7

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

 More jobs in operations

Stay in the field you know and move sideways rather than up.
If you leave this industry

Expertise in regulated quality systems transfers to other GxP industries, such as food and beverage, aerospace, or defence. It also applies to consulting work in quality and compliance. Demand for people who can build compliant digital quality infrastructure continues to grow.

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.