Job Description

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Summary

We are seeking a forward-thinking, detail-oriented, and structured Training and Document Management Business Adviser to join our team. In this critical role, you will ensure compliance with training and document management requirements for Pharmaceutical GxP and Business compliance processes while supporting efficient execution of Country Organisation Quality and Compliance activities. You will be instrumental in fostering a culture of operational excellence, maintaining high standards for quality systems, and enabling compliance with regulatory requirements.



The ideal candidate will thrive in dynamic, multi-entity environments, show proficiency in document control systems, and work proactively with associates across the business to ensure training readiness and document accuracy.
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About the Role

#LI-Hybrid

Key Responsibilities:

Ensure compliant and efficient execution of quality and compliance activities related to training and documentation systems. Support resolution of quality-related issues, including investigations, deviations, and CAPAs. Promote a "right-first-time" culture of quality compliance across the organization. Act as a recognized expert in training and document management, liaising with global teams and stakeholders. Coordinate training logistics, including onboarding, role updates, and course material preparation. Monitor training expiry dates and schedule refreshers to maintain compliance. Drive continuous improvement initiatives to streamline training processes. Manage the internal document system, ensuring documents are current, compliant, and properly archived. Prepare and support audits and inspections as a subject matter expert in training and documentation. Report and analyze KPIs related to training and document management, escalating risks and issues as needed.

Essential Requirements:

Degree in a Science or data management subject or equivalent 2-3 years' experience in a quality, document management, training coordination, or learning and development role. Knowledge of Pharmaceutical GxP requirements and/or business compliance processes. Previous experience administering or managing training for new starters, role changes, and operational teams. Exposure to continuous improvement initiatives within a compliance-driven environment is desirable. Professional fluency in English, with excellent verbal and written communication skills.

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network:

Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards:

Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards



Division
Operations
Business Unit
Universal Hierarchy Node
Location
United Kingdom
Site
London (The Westworks)
Company / Legal Entity
GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.