Regulatory Affairs Manager

Hayati; Manchester; On-site; GBP 65,000 - 105,000; Full time

Job summary

Hayati is seeking a Regulatory Affairs Manager / Senior Regulatory Affairs Specialist to support international market access and regulatory compliance for vaping, e-cigarette and nicotine-related products. Based in Manchester, this on-site role focuses on interpreting regulations, coordinating with laboratories and regulatory bodies, and guiding development and marketing teams to ensure compliance.

The successful candidate will have direct regulatory experience with vaping products and fluency

Qualifications

• Bachelor’s degree or higher in Regulatory Affairs, Chemistry, Toxicology, Pharmacy, Engineering, Tobacco Science, Law or similar.
• Regulatory affairs experience in product compliance or market access.
• Direct experience with vaping, e-cigarette, tobacco or related products.
• Strong understanding of e-cigarette/vaping regulations in at least one key region (UK/EU/US/Middle East).
• Familiarity with UK vaping product requirements (TPD) and US FDA requirements.
• Experience translating regulations and standards into test scopes, docs or market-entry plans.
• Experience coordinating labs, testing bodies, regulatory consultants or client projects.
• Ability to review test scopes and regulatory reports; laboratory work not required.
• Fluent written and spoken English.

Responsibilities

• Research, monitor and interpret vaping, e-cigarette and nicotine-product regulations across UK, Europe, US, Middle East and target markets.
• Maintain regulatory information and advise internal stakeholders on market-entry, product-testing, registration and documentation requirements.
• Liaise with overseas laboratories, testing providers, regulatory consultants and external organisations to confirm standards, testing scopes and timelines.
• Coordinate and monitor product testing, notification and registration projects; identify gaps and follow up on actions.
• Review testing plans, reports and supporting documents for regulatory adequacy.
• Provide regulatory guidance to Product Development, R&D, Quality and Supply Chain teams.
• Review packaging, labelling, warnings, descriptions and marketing claims from a regulatory perspective.
• Prepare regulatory summaries, internal guidance and training materials; deliver regular compliance training.

Education

Bachelor’s degree or higher

Tools

TPD knowledge

US FDA/PMTA understanding

Regulatory interpretation

Job description

Regulatory Affairs Manager / Senior Regulatory Affairs Specialist Vaping & Nicotine Products

Location:

Manchester, UK

Working arrangement:

On-site

Position Level

The successful candidate may be appointed at either Regulatory Affairs Manager or Senior Regulatory Affairs Specialist level, depending on their directly relevant industry experience, regulatory expertise and ability to independently manage international compliance projects.

Job Overview

The Regulatory Affairs Manager / Senior Regulatory Affairs Specialist will support the international market access and regulatory compliance of the company’s vaping, e-cigarette and nicotine-related products.

The role will focus on researching and interpreting regulatory requirements across global markets, identifying applicable product testing and registration requirements, coordinating with overseas laboratories and regulatory organisations, and providing practical compliance guidance to Product Development, R&D, Marketing teams.

This is a regulatory interpretation and compliance project role rather than a laboratory testing or instrument-operation position.

Key Responsibilities

• Research, monitor and interpret vaping, e-cigarette and nicotine-product regulations, policies and technical standards across the UK, Europe, the United States, the Middle East and other target markets.
• Maintain clear and organised regulatory information and advise internal stakeholders on market-entry, product-testing, registration and documentation requirements.
• Liaise with overseas laboratories, testing providers, regulatory consultants and relevant external organisations to confirm applicable standards, testing scopes, required documents and project timelines.
• Coordinate and monitor product testing, notification and registration projects, identify documentation or compliance gaps, and follow up on outstanding actions.
• Review testing plans, reports and supporting documents to confirm that they are appropriate and sufficiently complete for the intended regulatory or market-access purpose.
• Provide practical regulatory guidance to Product Development, R&D, Quality and Supply Chain teams to help ensure that products meet target-market requirements.
• Review product packaging, labelling, warnings, descriptions and marketing claims from a regulatory-compliance perspective.
• Prepare regulatory summaries, internal guidance, compliance updates and training materials, and deliver regular compliance training to relevant teams.

Qualifications and Experience

• Bachelor’s degree or above in Regulatory Affairs, Chemistry, Toxicology, Pharmacy, Engineering, Tobacco Science, Law or another relevant discipline.
• Relevant experience in regulatory affairs, product compliance, product registration, certification, regulatory consultancy or international market access.
• Direct experience involving vaping, e-cigarette, tobacco, nicotine or closely related regulated products.
• In-depth understanding of e-cigarette/vaping regulations and registration procedures in at least one target region (UK, EU, US, or Middle East).
• Familiarity with TPD-related requirements, UK vaping-product requirements and applicable US FDA requirements.
• Experience interpreting regulations and technical standards and translating them into product-testing, documentation or market-entry requirements.
• Experience coordinating laboratories, testing organisations, certification bodies, regulatory consultants or client regulatory projects.
• Ability to understand and review test scopes, technical reports and compliance documents. Direct operation of laboratory equipment is not required.
• Experience providing regulatory guidance to product-development, technical or commercial teams.
• Fluent written and spoken English.

Desirable Experience

• Direct experience with TPD, EU-CEG, MHRA vaping-product notification, FDA／PMTA or Middle Eastern registration projects.
• Previous employment with a testing laboratory, certification organisation, regulatory consultancy or electronic-cigarette manufacturer.
• Experience supporting inhalation devices, nicotine-delivery devices or nicotine-replacement-related products.

About PAX(Hayati®)

PAX, established in 2021 and headquartered in Hong Kong, operates globally. As a world-leading consumer electronics company, we focus on cutting-edge technologies.

Hayati®, PAX’s flagship brand, was born in the UK and has since grown into one of Britain’s best-known consumer electronics brands, with a strong and expanding international presence. Alongside Hayati®, we continue to incubate and develop a diverse portfolio of brands—including Quokka®, Moxy®, Liora®, Finebar® and Philia®—each designed for different lifestyles, moments and markets around the world.

In 2025, PAX completed a pre-IPO reorganisation of its corporate structure and governance framework, entering the preparation phase for a potential NASDAQ listing. PAX Group Holdings Limited leads the Group’s global governance and long-term strategy, with operating offices across the UK, Germany and the UAE to support local markets worldwide. The Group’s exclusive Chinese mainland partner, PAX Innovations (Shenzhen) Limited, provides integrated R&D, branding, supply chain and quality management services, connecting our global brands with world-class manufacturing capabilities.

Guided by integrity as our core value, PAX is driven by innovation, centred on users, and committed to building for the long term and sustainable development. By combining dependable products with trusted partnerships, we work alongside consumers, partners, and the broader industry to shape a credible, future-oriented global ecosystem.