22 Financial Regulations jobs in London

Job Details

Location: Hybrid (City of London office for a minimum of 3 days per week)

Length of Contract: Permanent (subject to a 6-month probation period)

Holidays: 25 days per year, plus a break between Christmas and New Year

Salary : £38,000 per annum

Start Date: December 2025/January 2026 (to be discussed)

About the role

The Association of Foreign Banks (AFB) is a trade association which represents 170 foreign banks in the UK, advocating for their interests to the Government and regulators (

You will work with the Director of Policy and Regulatory Affairs (and colleagues in the policy team) to: (a) provide access for AFB members to Government, policy makers and regulators; (b) aggregate and represent members’ views and opinions to help shape and influence the UK political and regulatory agenda on behalf of AFB members; and (c) monitor key regulatory and political developments that affect AFB members.

Your main responsibilities will include:

·    Regulatory and political monitoring

·    Assisting in drafting communications to AFB members

·    Attending meetings and roundtables to take notes and produce summaries

·    Desk based research of policy topics of relevance for non-UK headquartered banks

·    Drafting responses to consultation papers from regulators and Government

·    Drafting briefing notes

·    Drafting communications to external stakeholders such as the FCA, BoE, HMT

·    Creating presentations

·   Committee meeting and Policy event planning and organisation

·    Ad-hoc administrative tasks

The successful candidate will have:

·    a 2:1 (or equivalent) degree or postgraduate degree, ideally in economics, law or politics

·   some knowledge of wholesale bank/financial regulation issues in the UK, gained from study or from a previous or current role

·   an ability to read detailed information and draw out the key points in a concise manner

·   An interest in policy topics relevant to non-UK banks, e.g. ESG, artificial intelligence, visa and immigration, Senior Managers & Certification Regime, capital and supervisory requirements

·   excellent written and verbal communication and attention to detail

·   an ability to work to deadlines

What will make you stand out?

·   Evidence of a keen interest in banking and financial services/the City

·   at least three months’ experience in financial services and/or a public affairs department (e.g. an internship or work placement)

Closing Date for Applications : 15 September 2025

Interview Dates: Candidates selected for interviews will be contacted by Tuesday 23 September 2025

Application Details : To apply, please email your CV and a cover letter of a maximum of one page to 

Job Title:

Job Title: Regulatory Affairs Manager

Location: London

Hours: Monday to Friday

Hybrid: 2 days home working per week

Role Summary

This position is focused on ensuring regulatory compliance across food and feed safety, product quality, and integrity standards. The role involves monitoring legislative developments, supporting compliance strategies, and collaborating with internal teams and exter
Make your application after reading the following skill and qualification requirements for this position.
Please click on the apply button to read the full job description

Job title: Associate Director, Regulatory Affairs

A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical development plans to bring new products to patients in the most efficient way.

Responsibilities:

• Working together with multi-functional / geographical teams and other internal stakeholders to ensure that projects meet all key objectives and are delivered on time.
• Develop Regulatory Strategies for any new submissions as well as identifying risks.
• Contribute to the preparation of briefing packages for Scientific Advice, orphan drug designation, PRIME program.
• Participate during the interactions with Health Authorities.

Requirements:

• Substantial experience within Regulatory affairs and pharmaceutical industry.
• Extensive experience in the submission of new products.
• Experience working with new MA's.
• Experience interacting with EU/UK regulatory authorities.

Salary and benefits:

A highly competitive salary and wider benefits scheme is on offer.

To apply for this position or hear further details then please contact Freddie Hill via

G&L have an opportunity for a senior Regulatory professional with a strong background in CMC and biotechnology. Our UK team, which is based West London, has a number of projects with requirements in the coming months. Our projects are diverse and so we are considering all regulatory talent for our upcoming openings, which will include biotechnology and pharmaceutical as well as development and approved products.

As a G&L consultant, you will be working with a variety of clients, and your duties may include the following:

• Developing submission strategies and planning for post-approval CMC activities, including variations, renewals, market expansions, and annual reports.
• Evaluating change controls and providing regulatory assessments to classify quality changes in production and quality control.
• Supporting client project teams in the preparation of the CMC sections of all submission content to facilitate approvals and continued compliance.
• Reviewing key study reports (e.g. process validation, stability studies, analytical method validation) to ensure regulatory compliance.
• Developing and maintaining high quality, realistic Chemistry, Manufacturing & Control (CMC) plans for products in development.
• CMC authoring of Module 2.3 and Module 3 sections of the CTD dossier.
• Maintaining a positive and productive liaison with internal and external contacts. This may include clients, regulatory agencies, and related institutions.
• Attending formal interactions (face-to-face meetings, teleconferences etc.) with clients, and possibly, government agencies. Building positive working relationships with clients.
• Identifying gaps and risks in the CMC plans and working with the team to proactively develop solutions which will increase efficiency and minimize timelines.
• Assisting in the development of assessments and strategic regulatory plans for client product development programs.
• Reviewing CMC sections of BLA submissions and preparing gap analysis detailing requirements for submission to different jurisdictions.
• Participating in project teams and advising other departments on CMC regulatory issues and strategies, including manufacturing, supply chain, quality control, quality assurance, and other regulatory and local entities.

Person specification:

• A Life Science degree
• Around 5-10 years working knowledge of CMC regulatory Affairs including a minimum of 3 years working with Biotechnology products
• Experience in authoring technical / CMC parts of regulatory documents
• Knowledge of Health Canada, FDA, EMA and International Conference on Harmonization practices, regulations and guidelines and implementation into regulatory filings; integration of CMC data into regulatory and quality documents.
• Ability to maintain a high level of accuracy and attention to detail
• Problem solving, judgment and decision-making skills to seek creative solutions to issues surrounding on-time, on-budget and high-quality project outcomes
• Excellent planning, organization, interpersonal, time and change management skills.
• Working knowledge of RIM Systems including Veeva Vault
• Proficiency in MS-Office applications including Microsoft Word, Excel and PowerPoint.

If you would be interested in joining the team at G&L Scientific, please send your CV to today.

G&L Scientific is an equal opportunities employer and welcomes applicants from all sections of the community regardless of their gender, religious belief, political opinion, sexual orientation, disability, age, marital status or race. We recruit based on talent alone and firmly believe that an individual’s background should play no part in the recruitment and selection process.

I'm working on a new Associate Director Regulatory Affairs role with a fantastic global pharmaceutical manufacturing organisation based in London. Regulatory is one of the key functions being scaled within the organisation. This hire is a cornerstone role in that build-out and will have a massive impact on the future of the business.

Job Description Summary

• Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports.
• Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies.
• Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending registration and answers any questions.
• Serves as a regulatory liaison on the project team throughout the product lifecycle. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices.
• Serves as regulatory representative to marketing or research project teams and government regulatory agencies.
• Provides advice to development and/or marketing teams on manufacturing changes, line extensions, technical labelling, appropriate regulations and interpretations.
• Coordinates, reviews, and may prepare reports for submission

Must-Haves

• 6–10 years regulatory affairs experience in pharma/biotech.
• European regulatory experience (EMA procedures, centralised filings, scientific advice).
• Submissions across MAA, CTA, variations, RMPs (IND/global a bonus).
• Evidence of strategic contribution to regulatory development planning.
• Ability to represent regulatory in cross-functional teams.
• Strong communicator, able to liaise with HA and global counterparts.

Nice-to-Haves

• Direct EMA/MHRA negotiation experience.
• IND or global dossier exposure.
• Background in Cardiometabolics or related TAs.

If this is something you'd be interested in, get in touch with

Job Title: Global Regulatory Lead (GRL), Senior Regulatory Program Manager

Job Type: Full-time permanent position

Location: West London, UK – 3x a week in the office

Salary: Attractive salary plus benefits package

Working for one of the industry’s leading pharmaceutical companies, this is a fantastic opportunity to provide expert regulatory knowledge from pre-clinical through clinical studies to initial registration in key global markets.

Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending registration and answers any questions. Serves as a regulatory liaison on the project team throughout the product lifecycle. Ensures rapid and timely approval of new drugs, biologics/biotechnology, and/or medical devices, and continued approved status of marketed drugs or medical devices. Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Provides advice to development and/or marketing teams on manufacturing changes, line extensions, technical labelling, appropriate regulations, and interpretations. Coordinates, reviews, and may prepare reports for submission.

Role responsibilities:

• Drive global Regulatory Affairs strategies for the portfolio, including managing internal and external stakeholders.
• Lead interactions with the health authorities/ local agencies – MHRA, EMA & FDA. This will be including pre-submission meetings, pre-IND meetings, Scientific advice and type B/C meetings with the FDA.
• Support both early and late-stage development activities CTAs, IND, ODD, PIPS, IND, IMPD, and initial MAAs.
• Confident in doing submissions in global markets with a main focus on the UK, EU, US, and ROW.
• Support and lead cross functional team discussions with medical, quality, PV, and other departments.

Requirements:

• A scientific degree is essential.
• Proven track record of leading successful European (CP, DCP, MRP), European national and US submissions.
• Confident in leading global RA strategies.
• Knowledge of regulatory frameworks and external environments as it applies to project specific global regulatory strategy document (GRSD) delivery.
• Ability to drive new regulatory approaches to improve and expedite development products submissions to meet business/project objectives and patient needs.
• Ability to clearly convey and exchange information with internal and external stakeholders.

This role is a very senior role within the regulatory team and within any other business, it may be titled an Associate Director . You will need at least 8 years of relevant regulatory experience, ideally within a large pharmaceutical business.

All the Regulatory team members attend the office 3x a week, so you would be expected to attend the office on a hybrid basis in White City, London.

For more information, please reach out to me at